Original Research ARTICLE
β2-Adrenergic Receptor Activation Suppresses the Rat Phenethylamine Hallucinogen-Induced Head Twitch Response: Hallucinogen-Induced Excitatory Post-synaptic Potentials as a Potential Substrate
- 1Department of Psychiatry, School of Medicine, Ribicoff Research Facilities of the Connecticut Mental Health Center, Yale University, New Haven, CT, United States
- 2Astellas Pharma Global Development, Inc., Global Medical Science, CNS and Pain, Northbrook, IL, United States
- 3Department of Neurobiology, School of Medicine, Yale University, New Haven, CT, United States
5-Hydroxytryptamine2A (5-HT2A) receptors are enriched in layers I and Va of the rat prefrontal cortex and neocortex and their activation increases the frequency of glutamatergic excitatory post-synaptic potentials/currents (EPSP/Cs) onto layer V pyramidal cells. A number of other G-protein coupled receptors (GPCRs) are also enriched in cortical layers I and Va and either induce (α1-adrenergic and orexin2) or suppress (metabotropic glutamate2 [mGlu2], adenosine A1, μ-opioid) both 5-HT-induced EPSCs and head twitches or head shakes induced by the phenethylamine hallucinogen 2,5-dimethoxy-4-iodoamphetamine (DOI). Another neurotransmitter receptor also localized to apparent thalamocortical afferents to layers I and Va of the rat prefrontal cortex and neocortex is the β2-adrenergic receptor. Therefore, we conducted preliminary electrophysiological experiments with rat brain slices examining the effects of epinephrine on electrically-evoked EPSPs following bath application of DOI (3 μM). Epinephrine (0.3–10 μM) suppressed the late EPSPs produced by electrical stimulation and DOI. The selective β2-adrenergic receptor antagonist ICI-118,551 (300 nM) resulted in a rightward shift of the epinephrine concentration-response relationship. We also tested the selective β2-adrenergic receptor agonist clenbuterol and the antagonist ICI-118,551 on DOI-induced head twitches. Clenbuterol (0.3–3 mg/kg, i.p.) suppressed DOI (1.25 mg/kg, i.p.)-induced head twitches. This clenbuterol effect appeared to be at least partially reversed by the selective β2-adrenergic receptor antagonist ICI-118,553 (0.01–1 mg/kg, i.p.), with significant reversal at doses of 0.1 and 1 mg/kg. Thus, β2-adrenergic receptor activation reverses the effects of phenethylamine hallucinogens in the rat prefrontal cortex. While Gi/Go-coupled GPCRs have previously been shown to suppress both the electrophysiological and behavioral effects of 5-HT2A receptor activation in the mPFC, the present work appears to extend this suppressant action to a Gs-coupled GPCR. Furthermore, the modulation of 5-HT2A receptor activation-induced glutamate release onto mPFC layer V pyramidal neurons apical dendrites by a range GPCRs in rat brain slices appears to results in behaviorally salient effects of relevance when screening for novel CNS therapeutic drugs.
The common pharmacological action shared between the three major classes of serotonergic hallucinogens (indoleamines [e.g., psilocybin], phenethylamines [e.g., mescaline or DOI], and ergots [e.g., lysergic acid diethylamide (LSD)] is activation of the 5-HT2 family of receptors (Nichols, 2016). Activation of 5-HT2A receptors appears to mediate these psychotomimetic effects in humans and psychotomimetic-like effects in rodents (Canal and Morgan, 2012; Kometer and Vollenweider, 2016). The head twitch response induced by serotonergic hallucinogens in rodents frequently has been used as a psychotomimetic-like screen for potential antipsychotic drugs as part of a broader effort to understand psychotomimetic effects of serotonergic hallucinogens, NMDA receptor antagonists, and amphetamine. Conversely, blockade of 5-HT2A receptors may be involved in both the antipsychotic and antidepressant effects of many psychotherapeutic drugs, which implies that screening compounds on DOI-induced head twitches in rodents may have a broader significance than simply the treatment of psychosis (Marek et al., 1992, 2003). The role played by 5-HT2A receptors in modulating thalamocortical circuitry intimately related to arousal and attention may explain the diverse nature of effects seen by both activation and blockade of 5-HT2A receptors (Berendse and Groenewegen, 1991; Marek et al., 2001; Muller et al., 2017).
Regarding the circuitry of serotonergic hallucinogens in the prefrontal cortex (PFC)/neocortex, one prominent effect of 5-HT2A receptor activation in the PFC/neocortex is to increase the frequency of spontaneous 5-HT-induced EPSCs when recording from layer V pyramidal cells with slice preparations from adult rats (Aghajanian and Marek, 1997). While most 5-HT2A receptors in the PFC would appear to be post-synaptic in pyramidal cells, activation of a minority of medial prefrontal coretex (mPFC) 5-HT2A receptors appears to induce these spontaneous EPSCs from thalamocortical afferents, likely arising from the midline and intralaminar thalamic nuclei (Lambe and Aghajanian, 2001; Marek et al., 2001). A number of generally predominantly presynaptic receptors (μ-opiate, mGlu2, mGlu4, adenosine A1) suppress these 5-HT-induced EPSCs (Marek and Aghajanian, 1998a; Marek et al., 2000; Stutzman et al., 2001; Zhang and Marek, 2007). These effects appear to be analogous to the presynaptic effect of orexin2 receptor agonists to increase the frequency of spontaneous EPSCs from thalamocortical afferents arising from the midline and intralaminar thalamic nuclei (Lambe and Aghajanian, 2003). Activation of 5-HT2A receptors in PFC slice preparations enhances synaptic overflow of glutamate (Aghajanian and Marek, 1999; Lambe and Aghajanian, 2006; Aghajanian, 2009). Stimulation of the white matter deep to the cortex or in layer V coincident with application of DOI to the slice induces late EPSPs with different pharmacological sensitivity than both the evoked early EPSPs and polysynaptic EPSPs. 5-HT, itself, completely suppresses the evoked late EPSP elicited by stimulation of the white matter deep to the cortex combined with bath application of the phenethylamine hallucinogen DOI (Aghajanian and Marek, 1999). In contrast, the evoked early EPSP elicited under these conditions is minimally suppressed by several agonists which completely suppresses the evoked late EPSP. Gi/Go-coupled GPCR receptor activation (e.g., mGlu2, adenosine A1) also suppresses the evoked late EPSPs with greater potency and efficacy than the evoked early EPSCs. Thus, there appears to be some similar pharmacological sensitivity of the evoked late EPSPs compared to the spontaneous EPSCs induced by 5-HT2A receptor activation, though there are also differences as activation of NMDA NR2B receptors appears to play a permissive role in mediating the evoked late EPSCs (Lambe and Aghajanian, 2006).
Dopamine was previously found to suppress glutamate overflow in the PFC evoked by the combination of electrical stimulation and DOI, via dopamine D1/D5 receptors and the canonical cAMP transduction pathway (Lambe and Aghajanian, 2007). These effects are consistent with preliminary experiments testing epinephrine for efficacy in suppressing late EPSCs evoked by electrical stimulation and DOI while recording from layer V pyramidal cells of the mPFC. Agonists for μ-opiate, mGlu2, mGlu4, and adenosine A1 receptors suppress both electrophysiological effects and a behavior induced by 5-HT2A receptor activation (DOI-induced head twitches) that are mediated in part by output from the mPFC (Gewirtz and Marek, 2000; Klodzinska et al., 2002; Marek, 2003, 2009; Benneyworth et al., 2007; Wieronska et al., 2012; Slawinska et al., 2013). With this background, these preliminary electrophysiological experiments led to testing both the β2-adrenergic receptor agonist clenbuterol (Ordway et al., 1987) and the antagonist ICI-118,551 (Beer et al., 1988) in modulating DOI-induced head shakes in rats. The results of these experiments are consistent with the hypothesis that activation of β2-adrenergic receptors suppresses glutamate release induced by 5-HT2A receptor activation in the PFC.
Materials and Methods
Brain slices were prepared from male Sprague–Dawley rats (Harlan, Indianapolis, IN, United States; 120–200 g; n = 10) as described previously (Aghajanian and Rasmussen, 1989). Briefly, rats were anesthetized with chloral hydrate (400 mg/kg, i.p.) and decapitated. Coronal slices (500 μm) were cut with an oscillating-blade tissue slicer at a level corresponding to approximately 2.5 mm anterior to bregma. A slice containing the mPFC was then transferred to the stage of a fluid-gas interface chamber which had a constant flow of humidified 95% O2, 5% CO2. The slices were perfused in a chamber heated to 34°C with normal ACSF which consisted of (in mM) NaCl 126; KCl 3; CaCl2 2; MgSO4 2; NaHCO3 26; NaH2PO4 1.25; and D-glucose 10.
Intracellular recording and single-electrode voltage clamping were conducted in layer V pyramidal cells using an Axoclamp-2A (Axon Instruments, Inc., Foster City, CA, United States) as previously described (Aghajanian and Marek, 1997). Stubby electrodes (∼8 mm, shank to tip) with relatively low capacitance and resistance (30–60 MΩ) were filled with 1 M potassium acetate. Layer V pyramidal cells were recorded in current clamp mode. Evoked potentials were obtained while holding cells at -80 mV and stimulating the forceps minor in the white matter deep to the cortex with a bipolar tungsten electrode.
To uncover optimal stimulating sites, 5-HT (100 μM) was bath-applied while stimulating the forceps minor at a 0.1 Hz. 5-HT was turned off within 1–2 min while stimulation continued. Several minutes after turning off the 5-HT bath application, late EPSPs emerged in a fraction of cells. In those pyramidal cells in which late EPSPs did not emerge, the stimulating site was changed. In those cells in which late EPSPs emerged during the 5-HT washout period in response to the low-frequency stimulation, the combination of 0.1 Hz stimulation and DOI also evoked late EPSPs. In those cells in which late EPSPs did not emerge during the 5-HT washout period in response to the low-frequency stimulation, the combination of 0.1 Hz stimulation and DOI also did not evoke late EPSPs.
For those cells with late EPSPs induced by the combination of DOI and white matter stimulation, either a single concentration of epinephrine or an epinephrine concentration–response relationship was tested. The effect of epinephrine on the frequency of late EPSPs during 10 consecutive electrical stimulations (0.1 Hz) as well as the maximal amplitude (mV) of early and late EPSPs was measured. For these experiments, each concentration of epinephrine was bath-applied for 1 min prior and during stimulation of the deep white matter 10 times every 10 s. A 6–8 min washout interval was used between successively higher epinephrine concentrations. For a subset of these cells, blockade of the suppressant effect by epinephrine was attempted with the selective β2-adrenergic receptor antagonist ICI-118,551 (300 nM applied initially for 10 min and between successive epinephrine administrations). EC50s for the epinephrine concentration-response curves were calculated with GraphPad Prism. The pA2 value for ICI-118,551 was calculated by using the formula derived by Arunlakshana and Schild (1959); pA2 = log [Antagonist] – log (dr -1) where dose ratio (dr) was the EC50 for epinephrine in the presence of the ICI-118,551 divided by the EC50 for norepinephrine in the absence of ICI-118,551. The apparent Kb value for ICI-118,551 was calculated from the pA2 value (Arunlakshana and Schild, 1959).
Male Sprague–Dawley rats (n = 112) weighing between 150 and 300 g at the initial behavioral testing were used (Harlan, Indianapolis, IN, United States). They were housed in suspended stainless wire cages (18 cm × 36 cm × 20 cm) with two to four rats occupying each cage. The colony room was maintained at 20°C and relative humidity (60%). The room was illuminated 12 h/day (07:00–19:00). All rats had free access to laboratory chow (Teklad 4% Rat Diet) and water except during experimental sessions. All animals were treated in accord with the National Institutes of Health’s Guide for the Care and Use of Laboratory Animals. In addition, all protocols were approved by the Yale University Animal Care and Use Committee. All experiments were performed between 09:00 and 16:00. The animals were transferred to a clear polycarbonate cage (43 cm × 21.5 cm × 20 cm) with a sawdust-covered floor. All the rats were habituated to the testing environment with a saline injection at least several days prior to the first DOI/vehicle, DOI and clenbuterol/vehicle, or DOI/clenbuterol/ICI-188,551/vehicle injection. Clenbuterol (0.3–3 mg/kg, i.p.) was administered 15 min prior to DOI. The β2-adrenergic antagonist ICI-118,551 (0.01–1 mg/kg, i.p. was injected 30 min prior to DOI. The animals were observed during consecutive 5 min periods for a total of 30 min following the DOI injection. The observations began 1 min after injecting DOI to allow time for drug absorption. In addition to counting each head shake response, forward locomotion (movement from one end to the other end of the cage was scored as one cross) and rearing (rising up on hind limbs) were recorded.
A two-way ANOVA was carried out for the electrophysiological data to compare the epinephrine concentration–response curve on the early EPSPs vs. the late EPSPs. The late EPSPs data (n = 6) was analyzed with a one-factor ANOVA and comparisons to the control condition were made with the Dunnett test (p < 0.05).
A one-factor ANOVA was carried out for measurement of head shakes, rearing, and horizontal locomotor activity. The Dunnett test was used to test for specific comparisons to the DOI alone or the DOI/clenbuterol group, respectively. The effect of the β2-adrenergic receptor agonist clenbuterol was assessed using a between-subject design where a different cohort of rats was used for each dose (n = 12/group). The effect of the β2-adrenergic receptor antagonist ICI-118,559/vehicle with DOI/vehicle also was tested using a between-subject design (n = 16/group) in a separate second behavioral experiment. A slightly higher sample size was used for the β2-adrenergic antagonist experiment given the uncertainty regarding the occupancy of β2-adrenergic receptor at the doses chosen. The level of significance was set for p < 0.05.
Doses were calculated based on the salt forms. The drugs were dissolved in saline, neutralized to a pH of ∼7.4, and injected i.p. in a volume of 1 ml/kg body weight. The β2-adrenergic receptor agonist clenbuterol and the β2-adrenergic receptor antagonist ICI-118,559 were purchased from Tocris (Ballwin, MO) and Research Biochemical International (RBI; Natick, MA, United States), respectively. The 5-HT2A/2B/2C receptor partial agonist DOI, (±)-2,5-dimethoxy-4-iodoamphetamine hydrochloride, was purchased from RBI. A dose of DOI (1.25 mg/kg, i.p.) producing a near-maximum of head shakes over a 30 min period was chosen for experiments testing suppression of head shakes by clenbuterol (Gewirtz and Marek, 2000). DOI-induced head shakes increase in a monotonic dose-dependent manner through 9 mg/kg using Sprague–Dawley rats (Pranzatelli, 1990). For the electrophysiological experiments, (-) epinephrine bitartrate was purchased from Sigma (St. Louis, MO, United States). A 1 M stock solution was prepared with 10 mM sodium metabisulfite and diluted appropriately for the final solution bath applied to the slice. 5-Hydroxytryptamine (5-HT) creatine sulfate was purchased from Sigma Chemical, Co. (St. Louis, MO, United States). 5-HT was used only to find cells in which 5-HT2A receptor stimulation would induce late EPSCs.
Layer V pyramidal cells of the mPFC (predominantly in the prelimbic area; Cg3) were recorded in a zone ca 1/2–2/3 the distance between the pial surface and the subcortical white matter. The pyramidal cells in the present study had the following characteristics similar to that reported previously using this methodology with a resting potential of ∼71 mV; an action potential amplitude of ∼82 mV; an action potential duration of ∼0.8 ms (at half-amplitude); and an input resistance for a 0.4 nA test-pulse of ∼35 MΩ.
Epinephrine Selectively Suppresses Electrically-Evoked Late EPSPS after DOI
Epinephrine (10 μM, applied for 1 min before 10 successive stimulations of the white matter every 10 s) suppressed late EPSCs following DOI (3 μM × 10–15 min) either nearly completely or completely in 10 consecutive cells from 10 different rats. Epinephrine (0.3–10 μM) suppressed, in a monotonic concentration-dependent manner, the frequency of electrically-evoked late EPSPs following bath application of DOI (3 μM) to the slice for 10 min (n = 6, Figures 1A, 2). The EC50 for epinephrine in suppressing the frequency of late EPSPs (in an all-or-none fashion) was 1.65 μM. The one-factor ANOVA for the frequencies of late EPSCs was significant [F(3,6) = 11.35, p = 0.0069]. The 1, 3, and 10 μM epinephrine concentrations showed significant suppression of the late EPSCs compared to the control condition (p < 0.05).
FIGURE 1. Epinephrine selectively suppresses late EPSPs evoked by electrical stimulation/DOI. (A, top graph) Epinephrine (0.3–10 μM), in a monotonic dose-dependent manner, suppresses the frequency of late EPSPs induced by electrical stimulation (0.1 Hz × 10 Hz) after application of DOI (3 μM × 10 min) to rat medial prefrontal cortex (mPFC) slices (n = 6). (B, bottom graph) Epinephrine (1–10 μM) selectively suppresses the amplitude of late EPSPs evoked by electrical stimulation (0.1 Hz × 10) after application of DOI (3 μM × 10 min) in slices from three of the six rats shown above. While epinephrine did significantly suppress the early EPSPs at the two higher concentrations, epinephrine did not suppress the early EPSP induced by electrical stimulation after DOI by more than 29% in any of the 3 cells at any epinephrine concentration. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 compared to control using the Dunnett test.
FIGURE 2. Epinephrine selectively suppressed late EPSPs evoked by electrical stimulation/DOI with a rightward shift in the epinephrine concentration-response curve by the β2-adrenergic receptor antagonist ICI-118.551. (A) Epinephrine (0.3–10 μM) bath application suppressed the amplitude of DOI/electrically-evoked late EPSPs in a concentration-dependent manner in a cell from the rat mPFC. (B) In the same cell shown in (A), the β2-adrenergic receptor antagonist ICI-118,551 (300 nM × 10 min pretreatment, during and between epinephrine bath applications) induced a rightward shift of the epinephrine concentration-response curve with a pA2 of 7.37 (apparent Kb of 43 nM).
Measurement of both the electrically-evoked early EPSP and the late EPSP amplitude after DOI demonstrated the selectivity of epinephrine for suppression of the late EPSPs in a subset of these cells (n = 3; Figure 1B) as epinephrine suppressed the early EPSP by 18% compared to a maximal ∼91% suppression of the late EPSP at 10 μM. The EC50 for epinephrine in suppressing the maximal amplitude of late EPSPs was 2.06 μM. The mean basal magnitude of the electrically-evoked early EPSP and late EPSP after DOI administration was 5.3 (± 1.2, SD) and 9.8 (± 2.3, SD) mV. While significant effects were observed for time factor of early vs. late EPSCs [F(1,8) = 38.42, p = 0.0003] and the epinephrine concentration factor [F(3,8) = 17.75, p = 0.0007], the robust effect of epinephrine on late EPSCs is reflected in the significant interaction between the time and epinephrine concentration factors [F(3,8) = 7.80, p = 0.0092].
Experiments were conducted in three cells where the frequency of the late EPSCs were measured to suggest whether or not β2-adrenergic receptor activation might be mediating these effects of epinephrine. Bath application of ICI-118,551 (300 nM) blocked the suppressant action of epinephrine on the electrically-evoked late EPSP after DOI in three cells (Figure 3) with a mean pA2 value of 6.74 (SEM of 0.12). The apparent Kb in these three cells ranged from 105 to 217 nM. In two of these cells, the maximal amplitude of the late EPSCs was also measured. The pA2 calculated from the Schild equation was 7.37 and 6.22 in these two cells where the pA2 determined from the late EPSC frequency analysis was 6.98 and 6.58 respectively. The cell with a pA2 of 7.37 and apparent Kb of 43 nM from the late EPSP amplitude analysis is shown in Figure 2.
FIGURE 3. ICI-118,551 blocked the suppressant action of epinephrine on late EPSPs evoked by electrical stimulation/DOI. The shift in the epinephrine concentration-response suppression in the frequency of late EPSPs induced by electrical stimulation/DOI is shown for three cells (A–C) before and during bath application of the β-adrenergic receptor antagonist ICI-118,551 (300 nM). The pA2 calculated for each cell using the Schild equation is displayed for each cell.
DOI-Induced Head Twitches
The frequency of head twitches in vehicle-treated animals is less than 1.0 per 30 min observation periods (unpublished observations) while the frequency of DOI-induced head twitches in Sprague–Dawley rats generally ranges between 15 and 30 per 30 min observational periods. For the present experiments, DOI (1.25 mg/kg, i.p.; n = 12) induced approximately 25.9 ± 4.1 (SEM) head twitches/30 min. The β2-adrenergic receptor agonist clenbuterol (0.3–3 mg/kg, i.p.) suppressed DOI (1.25 mg/kg)-induced head twitches in a dose-dependent manner [F(3,33) = 3.58, p < 0.05; Figure 4]. The lowest effective clenbuterol dose (1.0 mg/kg) resulted in a similar effect (approximately 55% decrease) as the highest dose tested (3.0 mg/kg; Dunnett test, p < 0.05) compared to the frequency of head twitches induced by DOI (1.25 mg/kg) and the clenbuterol vehicle. These suppressant effects of clenbuterol on DOI-induced head twitches do not appear to be non-specific effects as clenbuterol did not alter the number of cage crosses [F(3,33) = 1.46, p > 0.2; Figure 5] or rearing [F(3,33) = 0.96; Figure 6] seen following the administration of DOI.
FIGURE 4. Clenbuterol (0.3–3.0 mg/kg, i.p.), via β2-adrenergic receptor activation, suppresses DOI (1.25 mg/kg, i.p.)-induced head shakes. (A, top graph) A dose-dependent suppression of DOI-induced head shakes is observed with significant suppression by clenbuterol of approximately 55% at the 1.0 and 3.0 mg/kg doses (n = 12/group). (B, bottom graph) In an entirely independent experiment, the β2-adrenergic receptor antagonist ICI-118,551 blocked the clenbuterol (1.0 mg/kg)-induced suppression of DOI (1.25 mg/kg)-induced head twitches in a dose-dependent manner with a significant effect at 1.0 mg/kg ICI-118,551 (n = 16/group). ∗p < 0.05 for comparison to DOI/clenbuterol vehicle or in comparison to DOI/clenbuterol/ICI-118,551 vehicle (bottom graph).
FIGURE 5. Neither clenbuterol (0.3–3.0 mg/kg, i.p.) or ICI-118,551 (0.1–1.0 mg/kg) altered horizontal locomotor activity after DOI. (A, top graph) No significant changes were observed in the frequency cage crosses over a 30 min period following vehicle or clenbuterol and DOI. (B, bottom graph) Similarly, no significant increases in the frequency of cage crosses over a 30 min period were observed following ICI-118,551.
FIGURE 6. Clenbuterol (0.3–3.0 mg/kg, i.p.) did not alter the frequency of rearing. (A, top graph) Clenbuterol did not alter the frequency of rearing over a 30 min period in rats administered DOI. (B, bottom graph) ICI-118,551 (0.1–1.0 mg/kg) increased rearing episodes after clenbuterol (1.0 mg/kg)/DOI (1.25 mg/kg). ∗p < 0.05 for comparison to DOI/clenbuterol/ICI-118,551 vehicle.
The selective β2-adrenergic receptor antagonist ICI-118,551 (0.01–1 mg/kg, i.p.) appeared to at least partially reverse the suppression by clenbuterol (1 mg/kg, i.p.) of DOI (1.25 mg/kg, i.p.)-induced head twitches in a dose-dependent manner [F(3,60) = 4.63, p < 0.01; Figure 4) in an entirely separate experiment (n = 16/each group) compared to the initial experiment demonstrating the suppressant action of clenbuterol (Figure 4, top graph). Thus, clenbuterol suppressed the number of DOI-induced head twitches by approximately 50% while ICI-118,551 (1 mg/kg) slightly more than doubled the number of DOI-induced head twitches observed following clenbuterol (1 mg/kg) in this second experiment with the antagonist. The highest ICI-118,551 dose tested significantly increased the number of DOI-induced head twitches after clenbuterol (1 mg/kg) compared to the suppressant effect of clenbuterol (1 mg/kg) alone on DOI-induced head twitches in this second experiment (Dunnett test, p < 0.05). ICI-118,551 had no effect on locomotor activity in rats administered DOI (Figure 5), though it did appear to increase rearing at the two higher doses (Figure 6).
The present results demonstrate that activation of β2-adrenergic receptors by clenbuterol suppressed head twitches induced by the phenethylamine hallucinogen DOI that are mediated by activation of 5-HT2A receptors. The attenuation of the clenbuterol suppressant action on DOI-induced head shakes by the selective β2-adrenergic receptor antagonist ICI-118,551 is consistent with the known in vivo action of clenbuterol as a selective β2-adrenergic agonist. Given that intracerebral administration of 5-HT2A agonists into the mPFC induces head twitches (Willins and Meltzer, 1997), these findings are consistent with the present observation that epinephrine selectively suppressed DOI-induced glutamate overflow when applied to rat prefrontal cortical slices. The pharmacological experiment with the β2-adrenergic agonist, ICI-118,551 and a previous report involving the cAMP transduction pathway (Lambe and Aghajanian, 2007) are consistent with an important modulatory action of β2-adrenergic receptor activation suppressing glutamate overflow induced by phenethylamine hallucinogens. However, further work will be required to confirm that these electrophysiological effects of epinephrine are mediated by β2-adrenergic receptors and not β1-adrenergic receptors.
Novel Receptor and Potential Transduction Pathway Suppressing DOI Effects
The present results raise the question of whether a receptor with a novel transduction pathway suppresses DOI-induced head twitches. Previous work has demonstrated that a number of canonical Gi/Go-coupled receptors suppress both the electrophysiological evidence for DOI-induced glutamate release and DOI-induced head twitches (Marek, 2017). This list of G-coupled receptors includes mGlu2, mGlu4, adenosine A1, and μ-opioid receptors, all which are known to have prominent or near-exclusive presynaptic actions in the CNS. In contrast, β2-adrenergic receptors are commonly coupled with Gs-proteins where they increase production of cAMP as the initial step of their transduction pathway. While current data does not rule out a role for β1-adrenergic receptors in suppressing DOI-induced head twitches, β-adrenergic receptor activation has been associated with an increase in glutamate release from cerebrocortical synaptosomes via an increase on cAMP and downstream effects on transmitter release machinery (Ferrero et al., 2013). Activation of dopamine D1/5 receptors or application of forskolin or 8-Br-cAMP also suppressed apparent glutamate overflow induced by DOI in rat PFC (Lambe and Aghajanian, 2007). These observations, coupled with the current observations for epinephrine and a β2-adrenergic receptor antagonist are all consistent with the hypothesis that activation of β2-adrenergic receptors with the accompanying increases in cAMP suppress both the electrophysiological (late EPSPs) and behavioral (head twitches) effects of serotonergic hallucinogens (Figure 7).
FIGURE 7. Model of glutamatergic input terminating in layers I and Va onto the apical dendrites of layer V pyramidal neurons of the prefrontal cortex (PFC) prelimbic region. Serotonergic hallucinogens (including DOI, LSD) increase glutamate overflow in layers I and Va of the PFC from glutamatergic terminals originating from the intralaminar and midline thalamic nuclei. 5-HT also increases this source of glutamate release. A number of Gi/Go-coupled receptors are able to suppress this glutamate overflow induced by 5-HT2A receptor activation including mGlu2, mGlu4, μ-opioid, adenosine A1, 5-HT1-like receptors. Several canonical Gs-coupled receptors (β2-adrenergic and dopamine D1/5 receptors) also suppress glutamate release from what may be the same afferents. The model shown assumes that all of these receptors are on the same terminals. Infusions of serotonergic hallucinogens into the mPFC (prelimbic region and anterior cingulate cortex) have been shown to induce the head twitch response in rodents (mPFC regions shown in right lower inset). The relationships shown for suppressing glutamate overflow onto layer V pyramidal cell apical inputs appear to also operate for suppression of the serotonergic hallucinogen-induced head twitch response in awake, behaving rodents (right top inset). ∗ Denotes those receptors shown to be decreased in layers I and Va of the rat PFC after midline thalamic lesions where an attenuation of 5-HT-induced spontaneous EPSCs is observed. In this model, there is no attempt to show the proportion of 5-HT2A receptors localized to the post-synaptic side of glutamatergic terminals (a large majority in addition to other 5-HT2A receptors localized to GABAergic interneurons and glial cells) compared to a putative minor population on the preterminal or terminal region of thalamocortical afferents.
The known regional and cellular distribution of these receptors suppressing DOI-induced glutamate overflow or DOI-induced head twitches is consistent with the importance of thalamocortical pathways in mediating these effects. The frequency of 5-HT-induced EPSCs is decreased by extensive thalamic lesions that damage the medial and intralaminar thalamic nuclei (Lambe and Aghajanian, 2001; Marek et al., 2001). These thalamic lesions were also found to decrease the amount of mGlu2/3 receptor or μ-opioid receptor binding in layers I and Va of the PFC (Marek et al., 2001), the cortical laminae with the richest innervation arising from these so-called non-specific thalamic nuclei (Berendse and Groenewegen, 1991). In the rat, β2-adrenergic receptors appear to be enriched in layers I and Va of the PFC/neocortex, although this mid-cortical enrichment is sometimes suggested to be layer IV (Rainbow et al., 1984; Booze et al., 1989). Accordingly, mRNA in situ hybridization studies have found a moderate β2-adrenergic receptor mRNA labeling in the midline and intralaminar thalamic nuclei in contrast to a relative lack of prefrontal cortical/neocortical labeling (Nicholas et al., 1993). The highest β2-adrenergic receptor mRNA labeling in the thalamus is for the midline and intralaminar thalamic nuclei which project to layer I and Va throughout the PFC/neocortex. A lesion study has verified that thalamic lesions decrease the amount of β2-adrenergic receptor binding in the PFC/neocortex (Vogt et al., 1992). Thus, β2-adrenergic receptors appear to be similarly located within thalamocortical afferents arising from the medial and intralaminar thalamic nuclei similar to mGlu2 and μ-opioid receptors.
Therapeutic Implications of Clenbuterol Suppression of DOI-Induced HTR
As discussed above, a range of agonists or positive allosteric modulators that activate Gi/Go-coupled receptors and β2-adrenergic receptor agonists appear to both suppress the electrophysiological effects of 5-HT or serotonergic hallucinogens in additional to suppressing DOI-induced head twitches (Marek, 2017). While DOI-induced head shakes or the HTR has been used as one component of a battery of paradigms screening for potential novel antipsychotic drugs, many antidepressant drugs also suppress DOI-induced head twitches. This primarily includes most tricyclic antidepressants and heterocyclic antidepressants (mirtazapine, mianserin, trazodone, and nefazodone) that all potently block 5-HT2A receptors). Modulation of 5-HT2A receptor responses in the PFC may be a key feature in detecting novel antidepressant drugs with serotonergic hallucinogen-induced head twitches. Interestingly, mGlu2 receptor PAMs, adenosine A1 receptor agonists, and β2-adrenoceptor agonists all induce antidepressant-like activity when administered to rodents trained on an operant screen for antidepressant drugs, the DRL 72-s schedule of reinforcement (O’Donnell, 1987; Nikiforuk et al., 2010; Fell et al., 2011; Marek, 2012). While an mGlu2 receptor PAM-tested in MDD did not result in clear antidepressant effects in a phase 2 trial, there are several small positive clinical trials with the β2-adrenergic receptor agonist salbuterol in depressed patients (Lecrubier et al., 1980; Simon et al., 1984). These results raise the possibility that the distribution of receptors suppressing DOI-induced head shakes by virtue of localization within critical microcircuitry (e.g., prefrontal cortical layer V pyramidal cells) might sculpture the phenotype of associated behavioral effects toward those with antidepressant-like and/or antipsychotic-like profiles.
The pro-cognitive profile of β2-adrenergic receptor agonists in primates and rodents raises the possibility that addition of β2-adrenergic receptor agonists to ongoing treatment with SSRIs may enhance antidepressant efficacy but also improve cognitive dysfunction associated with MDD. Specifically, either direct prefrontal infusions or systemic administration of clenbuterol to rats or primates improved working memory performance (Ramos et al., 2008). Speaking to differential effects of β-adrenergic receptor subtypes on cognition, either direct prefrontal infusions or systemic administration of the β1-adrenergic receptor antagonist betaxolol also improved the working memory of rodents or non-human primates (Ramos et al., 2005). These opposing actions of β-adrenergic receptor subtypes on cognition are consistent with the differential distribution of β-adrenergic receptor subtypes. The β2-adrenergic receptor protein and mRNA distribution was described above while β1-adrenergic receptor protein and mRNA are moderately localized throughout the PFC/neocortex and is also present in GABAergic cells of the reticular nucleus of the thalamus. This differential distribution of β-adrenergic receptor subtype protein and mRNA in thalamocortical circuits may serve as a foundation for the opposing actions of β-adrenergic receptor subtypes on executive functions reflecting prefrontal cortical function (Ramos and Arnsten, 2007). These relationships may be especially important when considering unmet medical needs of cognitive impairment in the treatment of major depressive disorder (MDD), including residual cognitive dysfunction following remission of other MDD symptoms.
A primary limitation in the interpretation of the results described here is that further electrophysiological studies directed at understanding the role of β2- and β1-adrenergic receptors in thalamocortical transmission are required that could also help determine the actual source of stimulated afferents to layer V pyramidal neurons. Furthermore, exploration with a wider range of β1-adrenergic and β2-adrenergic receptor antagonists would be one strategy to confirm whether there is an exclusive role for β2-adrenergic receptors in mediating the electrophysiological effects of epinephrine described here. Second, additional studies are required to determine whether other effects of clenbuterol or ICI-118,551 might also play a role in the behavioral effects. While ICI-118,551 at a 1 mg/kg dose did not reverse DOI-induced head twitches following clenbuterol to the same absolute magnitude of head twitches following DOI in the initial experiment with clenbuterol, the most likely explanation for this effect may be the two- to three-fold variability in the number of DOI-induced head twitches observed with independent cohorts of Sprague–Dawley rats. Accordingly, clenbuterol (1 mg/kg) suppressed DOI-induced head twitches by approximately 50% in one experiment while ICI-118,551 nearly doubled the frequency of head twitches observed after the administration of both DOI and clenbuterol (1 mg/kg) in another experiment. Third, an important step forward for the behavioral studies would be to extend these results toward an exploration of the 2nd messenger pathways involved. Fourth, these results bringing forth an additional class of receptor and GPCR-protein interactions with cortical 5-HT2A receptors would appear to challenge the view that these functional interactions between a number of Gq-coupled receptors inducing glutamate release and a number of receptors suppressing glutamate release can be explained simply by heteromeric receptor complexes (Gonzalez-Maeso et al., 2008; Moreno et al., 2011, 2012). Rather, the growing number of receptor interactions would suggest that simple functional interactions may play the primary role in these effects since evidence has only been advanced for interactions of the 5-HT2A receptor with mGlu2 or mGlu4 receptors (Delille et al., 2013; Marek, 2017). Alternatively, heteromeric complexes between 5-HT2A and mGlu2 receptors and simple functional interactions could both be relevant for these electrophysiological and behavioral relationships.
Activation of β2-adrenergic receptors appears to suppress DOI-induced head twitches. This behavior appears to involve the functional output of layer V pyramidal cells in the prelimbic region of the mPFC and the anterior cingulate. This novel finding for the β2-adrenergic receptor adds a Gs-type of protein-coupled receptor (β2-adrenergic) alongside a number of Gi/Go-coupled receptors (mGlu2, mGlu4, adenosine A1, u-opioid, 5-HT1A) that similarly act to suppress both the electrophysiological and a psychotomimetic-like behavioral effect of serotonergic hallucinogens in the mPFC. These relationships are consistent with clinical data supporting antipsychotic activity for mGlu2 and μ-opioid receptor agonists (and 5-HT2A receptor antagonists) and other clinical evidence suggesting antidepressant efficacy for 5-HT1A, β2-adrenergic, μ-opioid receptor agonists (Carlson and Simpson, 1963; Lecrubier et al., 1980; Simon et al., 1984; Bodkin et al., 1995; Marek and Aghajanian, 1998b; Patil et al., 2007; Kishi et al., 2014; Kinon et al., 2015).
GM and BR designed the research, performed the experiments, and analyzed and discussed the data. GM wrote the manuscript.
These studies were supported by PHS National Institute of Mental Health Grants K08 MH01551 and R01 MH62186, a National Alliance for Research on Schizophrenia and Depression Young Investigator Award, and the State of Connecticut Department of Mental Health and Addiction Services (GM). BR was supported by a Ford Foundation Predoctoral Fellowship.
Conflict of Interest Statement
A portion of the behavioral studies (involving the β2-adrenergic receptor antagonist ICI-118,551) were conducted while GM was initially employed by Pfizer.
The other author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The present experiments were conducted at the Ribicoff Research Facility of the Connecticut Mental Health Center and the Yale School of Medicine Department of Psychiatry. We thank Allyson Abo, Sara Heron, Angela Keene, Megan Lennon, and Matthew Trowbridge for assisting with the behavioral experiments.
Aghajanian, G. K., and Marek, G. J. (1997). Serotonin induces excitatory postsynaptic potentials in apical dendrites of neocortical pyramidal cells. Neuropharmacology 36, 589–599. doi: 10.1016/S0028-3908(97)00051-8
Aghajanian, G. K., and Marek, G. J. (1999). Serotonin, via 5-HT2A receptors, increases EPSCs in layer V pyramidal cells of prefrontal cortex by an asynchronous mode of glutamate release. Brain Res. 825, 161–171. doi: 10.1016/S0006-8993(99)01224-X
Aghajanian, G. K., and Rasmussen, K. (1989). Intracellular studies in the facial nucleus illustrating a simple new method for obtaining viable motoneurons in adult rat brain slices. Synapse 3, 331–338. doi: 10.1002/syn.890030406
Beer, M., Richardson, A., Poat, J., Iversen, L. L., and Stahl, S. M. (1988). In vitro selectivity of agonists and antagonists for beta1 - and beta2-adrenoceptor subtypes in rat brain. Biochem. Pharmacol. 37, 1145–1151. doi: 10.1016/0006-2952(88)90523-0
Benneyworth, M. A., Xiang, Z., Smith, R. L., Garcia, E. E., Conn, P. J., and Sanders-Bush, E. (2007). A selective positive allosteric modulator of metabotropic glutamate receptor subtype 2 blocks a hallucinogenic drug model of psychosis. Mol. Pharmacol. 72, 477–484. doi: 10.1124/mol.107.035170
Berendse, H. W., and Groenewegen, H. J. (1991). Restricted cortical termination fields of the midline and intralaminar thalamic nuclei in the rat. Neuroscience 42, 73–102. doi: 10.1016/0306-4522(91)90151-D
Booze, R. M., Crisostomo, E. A., and Davis, J. N. (1989). Species differences in the localization and number of CNS beta adrenergic receptors: rat versus guinea pig. J. Pharmacol. Exp. Ther. 249, 911–920.
Canal, C. E., and Morgan, D. (2012). Head-twitch response in rodents induced by the hallucinogen 2,5-dimethoxy-4-iodoamphetamine: a comprehensive history, a re-evaluation of mechanisms, and its utility as a model. Drug Test. Anal. 4, 556–576. doi: 10.1002/dta.1333
Delille, H. K., Mezler, M., and Marek, G. J. (2013). The two faces of the pharmacological interaction of mGlu2 and 5-HT2A - Relevance of receptor heterocomplexes and interaction through functional brain pathways. Neuropharmacology 70, 296–305. doi: 10.1016/j.neuropharm.2013.02.005
Fell, M. J., Witkin, J. M., Falcone, J. F., Katner, J. S., Perry, K. W., Hart, J., et al. (2011). N-(4-((2-trifluoromethyl)-3-hydroxy-4-(isobutyryl)phenoxy)methyl)benzyl)-1-methyl-1H-imidazole-4-carboxamide (THIIC), a novel metabotropic glutamate 2 potentiator with potential anxiolytic/antidepressant properties: in vivo profiling suggests a link between behavioral and central nervous system neurochemical changes. J. Pharmacol. Exp. Ther. 336, 165–177. doi: 10.1124/jpet.110.172957
Ferrero, J. J., Alvarez, A. M., Ramirez-Franco, J., Godino, M. C., Bartolome-Martin, D., Aguado, C., et al. (2013). β-Adrenergic receptors activate exchange protein directly activated by cAMP (Epac), translocate Munc13-1, and enhance the Rab3A-RIM1α interaction to potentiate glutamate release at cerebrocortical nerve terminals. J. Biol. Chem. 288, 31370–31385. doi: 10.1074/jbc.M113.463877
Gewirtz, J. C., and Marek, G. J. (2000). Behavioral evidence for interactions between a hallucinogenic drug and group II metabotropic glutamate receptors. Neuropsychopharmacology 23, 569–576. doi: 10.1016/S0893-133X(00)00136-6
Gonzalez-Maeso, J., Ang, R. L., Yuen, T., Chan, P., Weisstaub, N. V., Lopez-Gimenez, J. F., et al. (2008). Identification of a serotonin/glutamate receptor complex implicated in psychosis. Nature 452, 93–97. doi: 10.1038/nature06612
Kinon, B. J., Millen, B. A., Zhang, L., and McKinzie, D. L. (2015). Exploratory analysis for a targeted patient population responsive to the metabotropic glutamate 2/3 receptor agonist pomaglumetad methionil in schizophrenia. Biol. Psychiatry 78, 754–762. doi: 10.1016/j.biopsych.2015.03.016
Kishi, T., Meltzer, H. Y., Matsuda, Y., and Iwata, N. (2014). Azapirone 5-HT1A receptor partial agonist treatment for major depressive disorder: systematic review and meta-analysis. Psychol. Med. 44, 2255–2269. doi: 10.1017/S0033291713002857
Klodzinska, A., Bijak, M., Tokarski, K., and Pilc, A. (2002). Group II mGlu receptor agonists inhibit behavioral and electrophysiological effects of in mice. Pharmacol. Biochem. Behav. 73, 327–332. doi: 10.1016/S0091-3057(02)00845-6
Lambe, E. K., and Aghajanian, G. K. (2001). The role of Kv1.2-containing potassium channels in serotonin-induced glutamate release from thalamocortical terminals in rat frontal cortex. J. Neurosci. 21, 9955–9963.
Lambe, E. K., and Aghajanian, G. K. (2003). Hypocretin (orexin) induces calcium transients in single spines postsynaptic to identified thalamocortical boutons in prefrontal slice. Neuron 40, 139–150. doi: 10.1016/S0896-6273(03)00598-1
Lambe, E. K., and Aghajanian, G. K. (2006). Hallucinogen-induced UP states in the brain slice rat prefrontal cortex: role of glutamate spillover and NR2B-NMDA receptors. Neuropsychopharmacology 31, 1682–1689. doi: 10.1038/sj.npp.1300944
Lambe, E. K., and Aghajanian, G. K. (2007). Prefrontal cortical network activity: opposite effects of psychedelic hallucinogens and D1/D5 dopamine receptor activation. Neuroscience 145, 900–910. doi: 10.1016/j.neuroscience.2006.12.048
Lecrubier, Y., Puech, A. J., Jouvent, R., Simon, P., and Widlocher, D. (1980). A beta adrenergic stimulant (salbutamol) versus clomipramine in depression: a controlled study. Br. J. Psychiatry 136, 354–358. doi: 10.1192/bjp.136.4.354
Marek, G. J. (2009). Activation of adenosine1 (A1) receptors suppresses head shakes induced by a serotonergic hallucinogen in rats. Neuropharmacology 56, 1082–1087. doi: 10.1016/j.neuropharm.2009.03.005
Marek, G. J. (2012). Activation of adenosine1 receptors induces antidepressant-like, anti-impulsive effects on differential reinforcement of low-rate 72-s behavior in rats. J. Pharmacol. Exp. Ther. 341, 564–570. doi: 10.1124/jpet.112.191718
Marek, G. J. (2017). “Interactions of hallucinogens with the glutamatergic system: permissive network effects mediated through cortical layer V pyramidal neurons,” in Current Topics in Behavioral Neuroscience, eds M. A. Geyer, B. A. Ellenbroek, C. A. Marsden, T. R. E. Barnes, and S. L. Andersen (Berlin: Springer).
Marek, G. J., and Aghajanian, G. K. (1998a). 5-HT-induced EPSCs in neocortical layer V pyramidal cells: suppression by μ-opiate receptor activation. Neuroscience 86, 485–497. doi: 10.1016/S0306-4522(98)00043-8
Marek, G. J., Carpenter, L. L., McDougle, C. J., and Price, L. H. (2003). Synergistic action of 5-HT2A antagonists and selective serotonin reuptake inhibitors in neuropsychiatric disorders. Neuropsychopharmacology 28, 402–412. doi: 10.1038/sj.npp.1300057
Marek, G. J., McDougle, C. J., Price, L. H., and Seiden, L. S. (1992). A comparison of trazodone and fluoxetine: implications for a serotonergic mechanism of antidepressant action. Psychopharmacology 109, 2–11. doi: 10.1007/BF02245475
Marek, G. J., Wright, R. A., Gewirtz, J. C., and Schoepp, D. D. (2001). A major role for thalamocortical afferents in serotonergic hallucinogen receptor function in the rat neocortex. Neuroscience 105, 379–392. doi: 10.1016/S0306-4522(01)00199-3
Marek, G. J., Wright, R. A., Schoepp, D. D., Monn, J. A., and Aghajanian, G. K. (2000). Physiological antagonism between 5-hydroxytryptamine2A and group II metabotropic glutamate receptors in prefrontal cortex. J. Pharmacol. Exp. Ther. 292, 76–87.
Moreno, J. L., Holloway, T., Albizu, L., Sealfon, S. C., and Gonzalez-Maeso, J. (2011). Metabotropic glutamate mGlu2 receptor is necessary for the pharmacological and behavioral effects induced by hallucinogenic 5-HT2A receptor agonists. Neurosci. Lett. 493, 76–79. doi: 10.1016/j.neulet.2011.01.046
Moreno, J. L., Muguruzza, C., Umali, A., Mortillo, S., Holloway, T., Pilar-Cuellar, F., et al. (2012). Identification of three residues essential for 5-hydroxtryptamine 2A-metabotropic glutamate 2 (5-HT2A-mGlu2) receptor heteromerizaiton and its psychoactive behavioral function. J. Biol. Chem. 287, 44301–44319. doi: 10.1074/jbc.M112.413161
Muller, F., Lenz, C., Dolder, P., Lang, U. E., Schmidt, A., Liechti, M., et al. (2017). Increased thalamic resting-state connectivity as a core driver of LSD-induced hallucinations. Acta Psychiatic. Scand. 136, 648–657. doi: 10.1111/acps.12818
Nicholas, A. P., Pieribone, V. A., and Hokfelt, T. (1993). Cellular localization of messenger RNA for beta-1 and beta-2 adrenergic receptors in rat brain: an in situ hybridization study. Neuroscience 56, 1023–1039. doi: 10.1016/0306-4522(93)90148-9
Nikiforuk, A., Popik, P., Drescher, K. U., van Gaalen, M., Relo, A.-L., Mezler, M., et al. (2010). Effects of a positive allosteric modulatory of group II metabotropic glutamate receptors, LY487379, on cognitive flexibility and impulsive-like responding in rats. J. Pharmacol. Exp. Ther. 335, 665–673. doi: 10.1124/jpet.110.170506
Patil, S. T., Zhang, L., Martenyi, F., Lowe, S. L., Jackson, K. A., Andreev, B. V., et al. (2007). Activation of mGlu2/3 receptors as a new approach to treat schizophrenia: a randomized Phase 2 clinical trial. Nat. Med. 13, 1103–1108.
Pranzatelli, M. R. (1990). Evidence for involvement of 5-HT2 and 5-HT1C receptors in the behavioral effects of the 5-HT agonist 1-(2,5-dimethoxy-4-iodophenyl aminopropane)-2. Neurosci. Lett. 115, 74–80. doi: 10.1016/0304-3940(90)90520-J
Rainbow, T. C., Parsons, B., and Wolfe, B. B. (1984). Quantitative autoradiography of β1- and β2-adrenergic receptors in rat brain. Proc. Natl. Acad. Sci. U.S.A. 81, 1585–1589. doi: 10.1073/pnas.81.5.1585
Ramos, B. P., Colgan, L. A., Nou, E., and Arnsten, A. F. (2008). Beta2 adrenergic agonist, clenbuterol, enhances working memory performance in aging animals. Neurobiol. Aging 29, 1060–1069. doi: 10.1016/j.neurobiolaging.2007.02.003
Ramos, B. P., Colgan, L. A., Nou, E., Ovadia, S., Wilson, S. R., and Arnsten, A. F. (2005). The beta-1 adrenergic antagonist, betaxolol, improves working memory performance in rats and monkeys. Biol. Psychiatry 58, 894–900. doi: 10.1016/j.biopsych.2005.05.022
Simon, P., Lecrubier, Y., Jouvent, R., Puech, A., and Widlocher, D. (1984). “Beta-receptor stimulation in the treatment of depression,” in Frontiers in Biochemical and Pharmacological Research in Depression, ed. E. Usdin (New York, NY: Raven Press).
Slawinska, A., Wieronska, J. M., Stachowicz, K., Marciniak, M., Lason-Tyburkiewicz, M., Gruca, P., et al. (2013). The antipsychotic-like effects of positive allosteric modulators of metabotropic glutamate mGlu4 receptors in rodents. Br. J. Pharmacol. 169, 1824–1839. doi: 10.1111/bph.12254
Stutzman, G. E., Marek, G. J., and Aghajanian, G. K. (2001). Adenosine preferentially suppresses serotonin2A receptor-enhanced excitatory postsynaptic currents in layer V neurons of the rat medial prefrontal cortex. Neuroscience 105, 55–69. doi: 10.1016/S0306-4522(01)00170-1
Vogt, B. A., Crino, P. B., and Jensen, E. L. (1992). Multiple heteroreceptors on limbic thalamic axons: M2 acetylcholine, serotonin1B, β2-adrenoceptors, μ-opioid, and neurotensin. Synapse 10, 44–53. doi: 10.1002/syn.890100107
Wieronska, J. M., Stachowicz, K., Archer, F., Lech, T., and Pilc, A. (2012). Opposing efficacy of group III mGlu receptor activators, LSP1-2111 and AMN082, in animal models of positive symptoms of schizophrenia. Psychopharmacology 220, 481–494. doi: 10.1007/s00213-011-2502-2
Willins, D. L., and Meltzer, H. Y. (1997). Direct injection of 5-HT2A receptor agonists into the medial prefrontal cortex produces a head-twitch response in rats. J. Pharmacol. Exp. Ther. 282, 699–706.
Zhang, C., and Marek, G. J. (2007). Group III metabotropic glutamate receptor agonists selectively suppress excitatory synaptic currents in the rat prefrontal cortex induced by 5-hydroxytryptamine2A receptor stimulation. J. Pharmacol. Exp. Ther. 320, 437–447. doi: 10.1124/jpet.106.107490
Keywords: 2,5-dimethoxy-4-iodoamphetamine (DOI), head twitch response (HTR), epinephrine, layer V pyramidal neurons, medial prefrontal cortex (mPFC), excitatory post-synaptic potentials (EPSPs), clenbuterol, ICI-118,551
Citation: Marek GJ and Ramos BP (2018) β2-Adrenergic Receptor Activation Suppresses the Rat Phenethylamine Hallucinogen-Induced Head Twitch Response: Hallucinogen-Induced Excitatory Post-synaptic Potentials as a Potential Substrate. Front. Pharmacol. 9:89. doi: 10.3389/fphar.2018.00089
Received: 30 October 2017; Accepted: 26 January 2018;
Published: 08 February 2018.
Edited by:Rick Strassman, University of New Mexico School of Medicine, United States
Reviewed by:Clinton Canal, Mercer University, United States
Michael Andrew Benneyworth, University of Minnesota, United States
Copyright © 2018 Marek and Ramos. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Gerard J. Marek, email@example.com