Hypothesis and Theory ARTICLE
Cough-Anal Reflex May Be the Expression of a Pre-Programmed Postural Action
- Human Motor Control and Posture Lab, Section Human Physiology of the Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy
When coughing, an involuntary contraction of the external anal sphincter occurs, in order to prevent unwanted leakages or sagging of the pelvis muscular wall. Literature originally described such cough-anal response as a reflex elicited by cough, therefore identifying a precise cause-effect relationship. However, recent studies report that the anal contraction actually precedes the rise in abdominal pressure during cough expiratory effort, so that the sphincter activity should be pre-programmed. In recent years, an important family of pre-programmed muscle activities has been well documented to precede voluntary movements: these anticipatory actions play a fundamental role in whole body and segmental postural control, hence they are referred to as anticipatory postural adjustments (APAs). On these basis, we searched in literature for similarities between APAs and the cough-anal response, observing that both follow the same predictive homeostatic principle, namely that anticipatory collateral actions are needed to prevent the unwanted mechanical consequences induced by the primary movement. We thus propose that the cough-anal response also belongs to the family of pre-programmed actions, as it may be interpreted as an APA acting on the abdominal-thoracic compartment; in other words, the cough-anal response may actually be an Anticipatory Sphincter Adjustment, the visceral counterpart of APAs.
The cough-anal reflex has been described as the contraction of the external anal sphincter occurring when coughing (Meagher et al., 1993). Literature is however unclear in discriminating whether the action on the sphincter is a reflex response due to the abdominal and pelvic floor dynamics, or an integral component of the cough itself. According to the past studies, any maneuver causing an increase in abdominal pressure, like cough, Valsalva etc., determine a reflex contraction of perineal muscles (Parks et al., 1962; Bors, 1966; Deindl et al., 1993; Bø and Stien, 1994). Some authors even provided evidences that during voluntary cough the external anal sphincter is recruited after intercostals and abdominal muscles, suggesting that this response is mediated by a polysynaptic reflex (Chan et al., 2004). In both these hypotheses, a precise cause-effect relationship is identified, in which the reflex contraction of the sphincters prevent unwanted leakages or sagging of the muscular wall of the pelvis. On the contrary, recent literature reports that the sphincters contraction actually precede the rise in abdominal pressure during cough expiratory effort (Constantinou and Govan, 1982; Thind et al., 1990; Thind and Lose, 1992), also showing that the increase in anal or vaginal closing pressure precedes the cough motor act (Sapsford and Hodges, 2001) and that the external anal sphincter is recruited in advance of intercostals muscles (Deffieux et al., 2006). Based on their findings, Sapsford and Hodges (2001) and Deffieux et al. (2006) forwarded the alternative idea of a pre-programmed central control of the external anal sphincter activity for granting continence during cough.
From another perspective, if one examines the abdominal-thoracic compartment, a forceful increase of the internal pressure may be induced both by the respiratory muscles (diaphragm relaxation and internal intercostal muscles contraction) which promote the compression of the thoracic cavity, and/or by the abdominal wall muscles (contraction of rectus abdominis, transverse abdominis, external oblique muscle and internal oblique muscle) which press the abdominal organs cranially, reducing the volume of the thoracic cavity to help expel air, vomit, urine and feces from the body (Iscoe, 1998).
A different temporal and spatial recruitment of the wall muscles and of sphincters may thus lead to different behavioral results: expulsion of the air during speaking, singing, yelling or coughing (in this case perineal muscles and perineal sphincters should contract in synergy); vomit, when abdominal pressure increases and the lower esophageal sphincter is relaxed; defecation and micturition, when perineal muscles are contracted, to stiffen the pelvic floor, while perineal sphincters are relaxed, to offer an escape route to excretions. Not to mention the complex mechanism of foetal delivery, to which cooperates the uterine contraction.
Returning to the cough-anal reflex/response question, an important family of pre-programmed muscle contractions has been well documented when studying voluntary movements: these anticipatory adjustments play a fundamental role in whole body and segmental postural control (Bouisset and Do, 2008; Cavallari et al., 2016), so that they are referred to as anticipatory postural adjustments (APAs). By analogy, we propose that also the sphincter control may belong to the family of the pre-programmed actions, and in this view, the cough-anal reflex may be interpreted as an APA on the thoraco-abdominal compartment.
Anticipatory Postural Adjustments and Voluntary Movements
In humans, there are several examples of pre-programmed, anticipatory actions which accompany a willed movement. Indeed, APAs are usually described as unconscious muscular activities preceding the primary movement and aim to counterbalance the perturbation caused by it (for a review, see Massion, 1992; Bouisset and Do, 2008). APAs are so intimately linked to the motor program that the involuntary neural command to postural muscles is shared with the voluntary command to prime mover muscles (Bruttini et al., 2014). The importance of APAs is apparent when considering motion of one single limb (e.g., Belen’kii et al., 1967 for the upper limb; Alexeief and Naidel, 1972 for the lower limb), in this context, the main goal of APAs is to minimize the changes in the body center of mass, to keep its projection within the support area, and to counteract the self-initiated postural perturbation. APAs also contribute to initiate the displacement of the body center of mass when starting gait (Brenière et al., 1987) or whole body reaching movements (Stapley et al., 1998, 1999). These activities, called inter-limb APAs, set one or more fixation chains spreading over several muscles of different limbs. APAs may also precede movements of tiny masses, like a brisk flexion of the index-finger when performed in a seated position (Caronni and Cavallari, 2009). In this case, they are named intra-limb APAs as the fixation chain is limited to muscles acting on proximal joints (Cavallari et al., 2016). Taking into account the small mass of the moving segments, and the fact that this movement cannot affect the whole-body balance, the role of intra-limb APA has been attributed to the precision of the final movement (Bruttini et al., 2016). Note also that despite the different aim, inter- and intra-limb APAs share many behavioral properties: they are distributed to muscles of the same limb in which the movement occurs, precede the onset of the voluntary movement, are polarized according to the task direction in space, are scaled to the amplitude of the perturbation and adapt to changes in the postural requirement of the task (Cavallari et al., 2016).
Cough is a defensive reflex, triggered by sensory inputs arising from the airways, that generates a high velocity air flow so as to free the respiratory tract from whichever obstruction (for a review, see Ando et al., 2014). It consists of a modified respiratory act which starts with a profound preparatory inspiration phase, followed by a brief compressive phase, in which an expiratory effort is exerted against the closed glottis, and finally by an expulsive phase in which a sudden opening of the glottis is coupled to a quick and strong expiratory muscles contraction (Fontana and Lavorini, 2006).
Cough reflex, is aimed at protecting the respiratory tract from irritation agents, foreign bodies and microorganisms, either inhaled or in loco produced (Bolser and Davenport, 2002; Bessac and Jordt, 2010), such action escapes any voluntary control and its processing seems to be entirely based on brainstem structures (Baekey et al., 2001; Canning and Mori, 2010). Nevertheless, more and more literature reports that not only sensory and motor but also cognitive and affective mechanisms may play a role in controlling cough, being able either to promote or inhibit it (Widdicombe, 1995; Fong et al., 2004; Mazzone et al., 2007, 2011; Davenport, 2009). Cough, like most respiratory maneuvers, can be also initiated at will, indeed cough or cough-like maneuvers are quite common in non-verbal communication, e.g., to require attention or express disagreement, to pretend to be ill or underline the symptoms of a real disease.
Reflex and voluntary cough present important differences in several aspects. Apart from the fact that the former is triggered by a precipitating sensory stimulus while the latter is not, both types of cough require similar muscle groups, but voluntary coughing recruit such muscles according to a precise sequential order (Lasserson et al., 2006; for review see Magni et al., 2011). Moreover, the peak intra-abdominal pressure reached during reflex cough is higher than that reached during voluntary cough (Addington et al., 2008).
Several studies aimed at identifying the CNS structures that govern coughing and their neural interconnections. Although an extensive list of candidate structures have been proposed, detailed studies about the role of each structure are still missing, so that specific aspects such as the relative inter-structure connections and the temporal organization are not yet fully determined. Some recent insight has been provided by McGovern et al. (2012a,b), who used neurotropic viruses to map the interconnections between neuronal networks.
The sensory fibers of the vagal nerve than stem from the airways project to the trigeminal sensory and solitary tract nuclei. In turn, these nuclei project to the hypothalamus and to the parabrachial nuclei, to the thalamus and to subthalamic nuclei, as well as to the amygdala and up to several cortical areas, which include the somatosensory cortices as well as the cingulate, insular and orbital cortices (McGovern et al., 2012a). These data allowed Mazzone et al. (2013) to propose that two ascending pathways originate from the airways: the first that projects to the ventral and basal portion of the thalamus and then up to the somatosensory cortices, while the second crosses the medial and dorsal thalamus, reaching the insula, as well as the orbital and cingulated cortices.
Important results about the brainstem circuitry governing reflex cough have been obtained by employing pharmacological and electrophysiological techniques on deeply anesthetized or even decerebrate animals. Indeed, such experiments showed that the afferent inputs to the pontine and medullary nuclei are able to trigger a reconfiguration of the respiratory central pattern generator, changing its activity from the classical motor pattern that produce breathing to the specific pattern driving cough (Baekey et al., 2001, 2003; Canning et al., 2004; McGovern et al., 2012a). However, an in depth description of the brainstem mechanisms that control cough in the human being is still lacking.
In the human being, urge-driven cough may be not exclusively governed by brainstem reflex circuitries, as other hierarchically higher brain areas, such as the insular, cingulate and somatosensory cortices, may provide an important contribution (Mazzone et al., 2011). Even if the exact role of these cortical areas is still unclear, it may be conceived that they take part in controlling the accessory muscles in cough, as well as in arranging the voluntary control of cough. In support of such a proposal, Shima et al. (1991) reported that in monkeys the stimulation of the posterior insular cortex is able to induce contractions in the contralateral muscles. Similarly, the mid-cingulate cortex has been reported to be active when voluntarily coughing, and also during a voluntary sniff or breath (Simonyan et al., 2007; Mazzone et al., 2011). Finally, it is noteworthy that cough-like actions may be elicited in the anesthetized cat by stimulating the amygdala or the suprasylvian gyrus with electrical pulses, and that the reflex-cough, triggered by stimulating the superior laryngeal nerves (afferent components), is inhibited if a simultaneous stimulus is applied to the orbital or cingulate gyri (Kito et al., 1977; Kasé et al., 1984).
Pelvic Floor Muscles
Pelvic floor muscles are involved in the function of the lower urinary tract and lower digestive tract, as well as in sexual functions. Thus, their neural control, which is somatic in origin, must consider their involvement in visceral activity. A coordination with the autonomic motor nervous systems should then be previewed.
The function of pelvic floor/sphincter lower motor neurons is organized differently from other groups of motor neurons. In contrast with the reciprocal innervations, commonly observed in limb muscles, the neurons innervating each side of the pelvic floor must work in harmony and synchronously, as a functional unit. As an example, in continent women bilateral pubococcygei muscles contract simultaneously and so do both halves of the sphincter muscle (Deindl et al., 1993). But flexible activation patterns could be possible, due to the unilateral innervation of these muscles. Indeed, Kenton and Brubaker (2002) reported that levator ani and urethral sphincter may show differences in activation patterns. On voiding, the external urethral sphincter should relax, preceding the detrusor contraction, while the anal sphincter is tonically active; on the contrary, both sphincters relax when defecating (Read and Sun, 1990). It is also known that a voluntary inhibition of the urethral sphincter may be achieved even without actually voiding (Sundin and Petersén, 1975).
Reflex activity may be triggered by an increase of intra-abdominal pressure or by a distension of pelvic organs, but it cannot be excluded that long-loop pathways activated by noxious stimuli may contribute as well (McMahon et al., 1982). It has been also reported that reflex activity may be modulated by inhibitory descending pathways from the brainstem and the motor cortex (Mackel, 1979). In particular, the descending inhibitory projections from pontine tegmentum, via the commissural nucleus, seem to be crucial for a correct timing of the sphincter relaxation during voiding (Blok and Holstege, 1998). Importantly, the complex motor sequence which drives bladder and sphincter activity is also accompanied by coordinated postural changes (Stafford et al., 2012).
In addition, pelvic floor muscles have been shown to contribute to both postural and respiratory functions (Hodges et al., 2007). These authors indeed demonstrated that during voluntary arm movements the activation of Anterior Deltoid is preceded by EMG activity in pelvic floor muscles; these muscles are activated before the intra-abdominal pressure increases, also contributing to stiffen the sacroiliac joints, therefore such activity should actually be an APA. Hodges et al. (2007) also recorded pelvic floor muscles activity during quiet breathing and under increased dead-space condition, reporting that such activity was tailored according to the respiration phase, increasing together with abdominal muscles activity; a finding that suggests the presence of visceral APAs when breathing. Finally, it is important to note that when discussing the above results, these authors concluded for a pre-programmed control, in view of the observation (Constantinou and Govan, 1982) that during a cough the increase in urethral pressure precedes by ~200 ms the increase in bladder pressure.
Cough and Pelvic Floor Muscles Activity
According to the past literature, cough, Valsalva maneuver, and more generally, abdominal distension, determine a reflex contraction of perineal muscles (Parks et al., 1962; Bors, 1966; Deindl et al., 1993; Bø and Stien, 1994). In fact, cough determines an increase in abdominal pressure and subsequently an increase in pressure in the bladder and the rectum. But every increase in bladder or rectum pressure requires a simultaneous increase of contraction of the sphincters to prevent leakages or the sagging of the muscular wall of the pelvis. Thus, a contraction of striated urethral muscle or striated anal sphincter is required. Many electrophysiological studies have described these actions (Parks et al., 1962; Deindl et al., 1993; Meagher et al., 1993; Bø and Stien, 1994), defining them as reflex responses. In this regard, Chan et al. (2004) showed that the external anal sphincter is recruited after intercostals and rectus abdominis muscles, both during voluntary cough and sniff. Moreover, the latency between rectus abdominis and external anal sphincter activation decreased as the cough effort increased. These authors concluded for a polysynaptic origin of the cough-anal reflex, but also reported that the afferent pathway for such late external anal sphincter response does not involve sensory input from the anal mucosa. Therefore they suggested that the reflex afferent pathway could come from muscle spindles or other sensory receptors in pelvic floor muscles, ligaments and fascia, as well as from the viscera or bladder. Unfortunately, Chan et al. (2004) did not recorded intra-abdominal pressure, which is the most probable cause of excitation for all such sensory receptors.
On the contrary, during voluntary cough, an increase in intra-urethral pressure precedes (by 100–240 ms) the rise in bladder pressure in healthy volunteers (Constantinou and Govan, 1982; Thind et al., 1990; Thind and Lose, 1992) and electromyographic (EMG) activity of the urethral sphincter occurs before cough in women suffering stress incontinence (Roskar et al., 1981; Heidler et al., 1987; Thüroff et al., 1987). These results fits with the hypothesis forwarded by van der Kooi et al. (1984) that the increase in abdominal pressure should follow the contraction of pelvic floor muscles.
More recently, Sapsford and Hodges (2001) reported that cough, which induce a rise in gastric pressure, is preceded by a rise in anal or vaginal pressure. These authors also underlined that this response should thus be pre-programmed. Moreover, Deffieux et al. (2006) reported that, during voluntary cough in continent women, external anal sphincter activity increased not only before intra-abdominal pressure but also before intercostal muscle activity (latency ranging from 40 ms to 800 ms), a result in apparent contrast with that of Chan et al. (2004). Deffieux et al. (2006) actually provided a detailed critic of those results, underlining that Chan’s group analyzed just one subject, did not record intra-abdominal pressure and used needle electrodes for EMG recording, which just record activity from small areas of muscles, while surface electrodes are better adapted to obtain accurate measurements of whole muscle activity. Therefore, also these authors concluded for a pre-programmed central control of the external anal sphincter activity aiming to maintain continence. In addition, it has been demonstrated that pelvic floor muscle contraction not only anticipates, but is also proportional to the rise in intra-abdominal pressure caused by the cough effort (Amarenco et al., 2005), a finding that replicates a well known behavior of the APAs.
Finally, although many authors suggest that anticipatory activity in pelvic floor muscles cannot be a reflex response to the afferent input generated by the stretch of the thoracic or abdominal muscles, since it precedes both voluntary and involuntary abdominal muscles recruitments, nobody explicitly states that the anticipatory pelvic floor response during cough may be an anticipatory component of the cough itself involving higher integrative centers. In this regard, it is interesting to note that the correlation between the rectus abdominis to external anal sphincter latency and the cough effort reported by Chan et al. (2004) is also consistent with the correlation between the APAs to prime mover latency and movement speed demonstrated by Horak et al. (1984).
Ontogenesis of Postural and Sphincter Anticipatory Adjustments
The control of body position in space develops with different intensity during life span (Assaiante et al., 2005; Soberaa et al., 2011). As an example, Zaino and McCoy (2008) showed that young healthy children (6–8 years old) exhibit much higher variability of posture control than older healthy children (10–12 years old). It is also reported that the age 7–9 years is an important period of their life in which children master postural control (Massion, 1998). Moreover, Schmitz et al. (1999) showed that children 3–4 years old develop APA, although they show coexistence of both adult-like and immature patterns, concluding that this anticipatory activities are being set up and that children are progressively mastering them.
It is also well known that all children have wetting and/or soiling accidents at one time or another. Achievement of urinary continence is an important developmental step that most children attain with the assistance of their parents and caregivers, however literature reports that about 15%–20% of children become partially toilet trained but continue to have wetting accidents even after the age 5 (Issenman et al., 1999). The first awareness of bladder and rectal functions usually occur between one and two years of age. The neural mechanisms involved in the storage and periodic elimination of urine undergo marked changes during prenatal and postnatal development (de Groat, 2002; Jansson et al., 2005). In the first years of life, voiding is controlled by a primitive spinal reflex pathway. Voluntary control over striated muscle sphincter usually occurs by the age of 3 years (Sillén, 2004). As the human CNS matures, higher brain centers contribute in modulating reflex voiding (see Figure 7 of Fowler et al., 2008). In adults, injury or disease of the nervous system can lead to the re-emergence of primitive reflexes Geirsson et al., 1993; Jiang et al., 2002).
Changes in brain structure are continuous throughout life (Chugani et al., 1987; Giedd et al., 1996). By the age 2, the brain has reached 75% of its adult weight (Carmichael, 1990) and the processes of synaptic pruning and cell death are most active during these early years (Huttenlocher, 1979; Huttenlocher et al., 1982). During the school-age years, strong signs of brain maturation are appreciable, especially in its connectivity (Lebel et al., 2008). MRI measures of the structure in fibers tracts correlate with behavioral indices that also change in this period (Schmithorst and Yuan, 2010; Tamnes et al., 2010a,b). Later changes involve the associative neocortex, which continues to develop well into the third decade (Yakovlev and Lecours, 1967), and the corpus callosum, which connects all major subdivisions of the cerebrum (Pujol et al., 1993).
Thus, before school-age all kinds of anticipatory actions, preceding primary movements, seems to be immature, either because the whole system is not still developed or because a part of it is not properly functioning. The achievement of a complete action (anticipatory and willed; postural or non-postural), therefore requires repetition learning (Draganski et al., 2004) and memory (Takeuchi et al., 2010).
Similarities between APAs and Cough-Anal Response
As shown above, APAs and cough-anal response share many common features: they are both anticipatory with respect to the primary movement, so that they cannot be reflex responses but must be pre-programmed; they both prevent unwanted mechanical consequences (postural perturbation or sphincter leaking); they are both scaled to the amplitude of the perturbation; and finally, they seem to follow the same ontogenetic steps.
Indeed, a conceptual similarity may be envisaged among inter-limb APAs, intra-limb APAs and the anal response. In fact, in all cases a single predictive homeostatic principle (Moore-Ede, 1986; Freddolino and Tavazoie, 2012) seems to be followed, namely that anticipatory collateral actions are needed to correctly perform the primary movement.
In the case of inter-limb APAs, that minimize the changes of the body center of mass and that counteract the self-initiated postural perturbation, this principle provides the maintenance of stability (equilibrium) of the whole body during an action (Massion, 1992; Bouisset and Do, 2008). These APAs spread over several muscles of different limbs, creating one or more long fixation chains.
In the case of intra-limb APAs, that maintain the stability of the different segments of a single limb, it means to successfully carry through a precise and coordinated movement (Caronni and Cavallari, 2009; Caronni et al., 2013; Bruttini et al., 2016; Cavallari et al., 2016). These APAs spread over several muscles of the same limbs, creating short fixation chains.
In the case of the anal or urinary responses, the anticipatory contraction of the sphincter permits to prevent fecal or urinary leakage during an increase of abdominal pressure, due to a sudden action. A behavior that should be defined anticipatory adjustment as well.
A final comment deserves the possible neural networks that may be involved in the control of postural and sphincter muscles. Indeed, some analogies may be directly outlined, while other may be actually tested. First, as mentioned in the “Cough” section, animal experiments showed that the afferent inputs to the pontine and medullary nuclei are able to trigger a reconfiguration of the respiratory central pattern generator, changing its breathing activity into a cough pattern (Baekey et al., 2001, 2003; Canning et al., 2004; McGovern et al., 2012a). In parallel, it has been shown that the automatic gait pattern of the locomotion central pattern generator may be influenced by pontine neurons (for a review, see Takakusaki, 2017). However, the advanced pre-programmed control of posture required for skilled and goal-directed movements involve many cortical areas, as well as basal ganglia and cerebellum (see Takakusaki, 2017). In this regard, the involvement of supplementary motor area and cerebellum in APAs control has been experimentally demonstrated by Bolzoni et al. (2015) and Bruttini et al. (2015). It would then be interesting to test if magnetic or DC stimulation of these structures would produce comparable effects on the anticipatory recruitment of postural muscles and of external sphincters, during both voluntary movements and respiratory/cough tasks.
On these basis, it is proposed that a common pre-programmed (i.e., feed-forward) mechanism may govern several kinds of anticipatory actions. In fact, in all cases the brain seems to control in the same way the general predictive homeostasis of the body, accomplishing movements either voluntary- or urge-driven. Thus, Anticipatory Sphincter Adjustments are likely the visceral counterpart of APAs. Of course, this speculative conclusion is just an hypothesis, which needs further experimental testing. Indeed, it could be interesting to investigate the EMG activity of visceral muscles, such as pelvic floor muscles, during other movements like hiccupping or chest vs. diaphragmatic breathing, so as to ascertain if such activities are actually anticipatory also in these conditions. Other evidences may come from testing if stimulation of the supplementary motor area or the cerebellum would affect in parallel the activation of both postural muscles and external sphincters. Indeed such finding would strengthen the analogy between the cough-anal response and the APAs.
PC proposed the idea. PC and RE collected and critically analyzed the literature. All authors contributed in writing and discussing the manuscript. All authors approved the final version and agree to be accountable for all aspects of this work.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Thanks to prof. Fausto Baldissera and prof. Edgardo D’Angelo for their valuable and detailed comments and suggestions on the manuscript. We are also grateful to Dr. Alex P. Moorhead for his helpful comments on an earlier version of this manuscript and for his precious assistance in improving the writing clarity and English style.
Amarenco, G., Ismael, S. S., Lagauche, D., Raibaut, P., Rene-Corail, P., Wolff, N., et al. (2005). Cough anal reflex: strict relationship between intravesical pressure and pelvic floor muscle electromyographic activity during cough. Urodynamic and electrophysiological study. J. Urol. 173, 149–152. doi: 10.1097/01.ju.0000147305.00443.df
Ando, A., Farrell, M. J., and Mazzone, S. B. (2014). Cough-related neural processing in the brain: a roadmap for cough dysfunction? Neurosci. Biobehav. Rev. 47, 457–468. doi: 10.1016/j.neubiorev.2014.09.018
Assaiante, C., Mallau, S., Viel, S., Jover, M., and Schmitz, S. (2005). Development of postural control in healthy children: a functional approach. Neural Plast. 12, 109–118; discussion 263–272. doi: 10.1155/np.2005.109
Baekey, D. M., Morris, K. F., Gestreau, C., Li, Z., Lindsey, B. G., and Shannon, R. (2001). Medullary respiratory neurones and control of laryngeal motoneurones during fictive eupnoea and cough in the cat. J. Physiol. 534, 565–581. doi: 10.1111/j.1469-7793.2001.t01-1-00565.x
Baekey, D. M., Morris, K. F., Nuding, S. C., Segers, L. S., Lindsey, B. G., and Shannon, R. (2003). Medullary raphe neuron activity is altered during fictive cough in the decerebrate cat. J. Appl. Physiol. 94, 93–100. doi: 10.1152/japplphysiol.00341.2002
Bessac, B. F., and Jordt, S. E. (2010). Sensory detection and responses to toxic gases: mechanisms, health effects, and countermeasures. Proc. Am. Thorac. Soc. 7, 269–277. doi: 10.1513/pats.201001-004SM
Bø, K., and Stien, R. (1994). Needle EMG registration of striated urethral wall and pelvic floor muscle activity patterns during cough, Valsalva, abdominal, hipadductor, and gluteal muscle contractions in nulliparous healthy females. Neurourol. Urodyn. 13, 35–41. doi: 10.1002/nau.1930130106
Bolzoni, F., Bruttini, C., Esposti, R., Castellani, C., and Cavallari, P. (2015). Transcranial direct current stimulation of SMA modulates anticipatory postural adjustments without affecting the primary movement. Behav. Brain Res. 291, 407–413. doi: 10.1016/j.bbr.2015.05.044
Bruttini, C., Esposti, R., Bolzoni, F., and Cavallari, P. (2014). Ischemic block of the forearm abolishes finger movements but not their associated anticipatory postural adjustments. Exp. Brain Res. 232, 1739–1750. doi: 10.1007/s00221-014-3866-4
Bruttini, C., Esposti, R., Bolzoni, F., and Cavallari, P. (2016). Higher precision in pointing movements of the preferred vs. non-preferred hand is associated with an earlier occurrence of anticipatory postural adjustments. Front. Hum. Neurosci. 10:365. doi: 10.3389/fnhum.2016.00365
Bruttini, C., Esposti, R., Bolzoni, F., Vanotti, A., Mariotti, C., and Cavallari, P. (2015). Temporal disruption of upper-limb anticipatory postural adjustments in cerebellar ataxic patients. Exp. Brain Res. 233, 197–203. doi: 10.1007/s00221-014-4103-x
Canning, B. J., Mazzone, S. B., Meeker, S. N., Mori, N., Reynolds, S. M., and Undem, B. J. (2004). Identification of the tracheal and laryngeal afferent neurones mediating cough in anesthetized guinea-pigs. J. Physiol. 557, 543–558. doi: 10.1113/jphysiol.2003.057885
Carmichael, A. (1990). “Physical development and biological influences,” in Handbook of Studies in Child Psychiatry, eds B. Tonge, G. D. Burrows and J. S. Werry (Amsterdam, Holland: Elsevier), 119–136.
Caronni, A., Bolzoni, F., Esposti, R., Bruttini, C., and Cavallari, P. (2013). Accuracy of pointing movements relies upon a specific tuning between APAs and prime mover activation. Acta Physiol. 208, 111–124. doi: 10.1111/apha.12081
Cavallari, P., Bolzoni, F., Bruttini, C., and Esposti, R. (2016). The organization and control of intra-limb anticipatory postural adjustments and their role in movement performance. Front. Hum. Neurosci. 10:525. doi: 10.3389/fnhum.2016.00525
Chan, C., Ponsford, S., and Swash, M. (2004). The anal reflex elicited by cough and sniff: validation of a neglected clinical sign. J. Neurol. Neurosurg. Psychiatry 75, 1449–1451. doi: 10.1136/jnnp.2003.032110
Constantinou, C. E., and Govan, D. E. (1982). Spatial distribution and timing of transmitted and reflexly generated urethral pressures in healthy women. J. Urol. 127, 964–969. doi: 10.1016/s0022-5347(17)54148-8
Deffieux, X., Raibaut, P., Rene-Corail, P., Katz, R., Perrigot, M., Ismael, S. S., et al. (2006). External anal sphincter contraction during cough: not a simple spinal reflex. Neurourol. Urodyn. 25, 782–787. doi: 10.1002/nau.20228
Deindl, F. M., Vodusek, D. B., Hesse, U., and Schüssler, B. (1993). Activity patterns of pubococcygeal muscles in nulliparous continent women. Br. J. Urol. 72, 46–51. doi: 10.1111/j.1464-410x.1993.tb06455.x
Freddolino, P. L., and Tavazoie, S. (2012). Beyond homeostasis: a predictive-dynamic framework for understanding cellular behavior. Annu. Rev. Cell. Dev. Biol. 28, 363–384. doi: 10.1146/annurev-cellbio-092910-154129
Giedd, J. N., Snell, J. W., Lange, N., Rajapakse, C. H., Casey, B. J., Kozuch, P. L., et al. (1996). Quantitative magnetic resonance imaging of human brain development: ages 4–18. Cereb. Cortex 6, 551–560. doi: 10.1093/cercor/6.4.551
Heidler, H., Casper, F., and Thuroff, J. W. (1987). Role of striated sphincter muscle in urethral closure under stress conditions: an experimental study. Urol. Int. 42, 195–200. doi: 10.1159/000281894
Horak, F. B., Esselman, P., Anderson, M. E., and Lynch, M. K. (1984). The effects of movement velocity, mass displaced, and task certainty on associated postural adjustments made by normal and hemiplegic individuals. J. Neurol. Neurosurg. Psychiatry 47, 1020–1028. doi: 10.1136/jnnp.47.9.1020
Huttenlocher, P. R., de Courten, C., Garey, L. J., and Van der Loos, H. (1982). Synaptogenesis in human visual cortex—evidence for synapse elimination during normal development. Neurosci. Lett. 33, 247–252. doi: 10.1016/0304-3940(82)90379-2
Issenman, R. M., Filmer, R. B., and Gorski, P. A. (1999). A review of bowel and bladder control development in children: how gastrointestinal and urologic conditions relate to problems in toilet training. Pediatrics 103, 1346–1352.
Jansson, U. B., Hanson, M., Sillen, U., and Hellström, A. L. (2005). Voiding pattern and acquisition of bladder control from birth to age 6 years—a longitudinal study. J. Urol 174, 289–293. doi: 10.1097/01.ju.0000161216.45653.e3
Kasé, Y., Kito, G., Miyata, T., and Takahama, K. (1984). Influence of cerebral cortex stimulation upon cough-like spasmodic expiratory response (SER) and cough in the cat. Brain Res. 306, 293–298. doi: 10.1016/0006-8993(84)90378-0
Kenton, K., and Brubaker, L. (2002). Relationship between levator ani contraction and motor unit activation in the urethral sphincter. Am. J. Obstet. Gynecol. 187, 403–406. doi: 10.1067/mob.2002.123939
Kito, G., Kasé, Y., Miyata, T., and Takahama, K. (1977). Neural mechanism for production of spasmodic expiratory response like cough induced by amygdala stimulation in the cat. I. Pathways from the amygdala to the lower brain stem. Arch. Int. Pharmacodyn. Ther. 229, 116–128.
Lasserson, D., Mills, K., Arunachalam, R., Polkey, M., Moxham, J., and Kalra, L. (2006). Differences in motor activation of voluntary and reflex cough in humans. Thorax 6, 699–705. doi: 10.1136/thx.2005.057901
Lebel, C., Walker, L., Leemans, A., Phillips, L., and Beaulieu, C. (2008). Microstructural maturation of the human brain from childhood to adulthood. Neuroimage 40, 1044–1055. doi: 10.1016/j.neuroimage.2007.12.053
Magni, C., Chellini, E., Lavorini, F., Fontana, G. A., and Widdicombe, J. (2011). Voluntary and reflex cough: similarities and differences. Pulm. Pharmacol. Ther. 24, 308–311. doi: 10.1016/j.pupt.2011.01.007
Mazzone, S. B., McGovern, A. E., Cole, L. J., and Farrell, M. J. (2011). Central nervous system control of cough: pharmacological implications. Curr. Opin. Pharmacol. 11, 265–271. doi: 10.1016/j.coph.2011.05.005
Mazzone, S. B., McGovern, A. E., Yang, S. K., Woo, A., Phipps, S., Ando, A., et al. (2013). Sensorimotor circuitry involved in the higher brain control of coughing. Cough 9:7. doi: 10.1186/1745-9974-9-7
Mazzone, S. B., McLennan, L., McGovern, A. E., Egan, G. F., and Farrell, M. J. (2007). Representation of capsaicin-evoked urge-to-cough in the human brain using functional magnetic resonance imaging. Am. J. Respir. Crit. Care Med. 176, 327–332. doi: 10.1164/rccm.200612-1856oc
McGovern, A. E., Davis-Poynter, N., Farrell, M. J., and Mazzone, S. B. (2012a). Transneuronal tracing of airways-related sensory circuitry using herpes simplex virus 1, strain H129. Neuroscience 207, 48–66. doi: 10.1016/j.neuroscience.2012.01.029
McGovern, A. E., Davis-Poynter, N., Rakoczy, J., Phipps, S., Simmons, D. G., and Mazzone, S. B. (2012b). Anterograde neuronal circuit tracing using a genetically modified herpes simplex virus expressing EGFP. J. Neurosci. Methods 209, 158–167. doi: 10.1016/j.jneumeth.2012.05.035
McMahon, S. B., Morrison, J. F., and Spillane, K. (1982). An electrophysiological study of somatic and visceral convergence in the reflex control of the external sphincters. J. Physiol. 328, 379–387. doi: 10.1113/jphysiol.1982.sp014271
Pujol, J., Vendrell, P., Junque, C., Martí-Vilalta, J. L., and Capdevila, A. (1993). When does human brain development end? Evidence of corpus callosum growth up to adulthood. Ann. Neurol. 34, 71–75. doi: 10.1002/ana.410340113
Schmitz, C., Martin, N., and Assaiante, C. (1999). Development of anticipatory postural adjustments in a bimanual load-lifting task in children. Exp. Brain Res. 126, 200–204. doi: 10.1007/s002210050729
Shima, K., Aya, K., Mushiake, H., Inase, M., Aizawa, H., and Tanji, J. (1991). Two movement-related foci in the primate cingulate cortex observed in signal-triggered and self-paced forelimb movements. J. Neurophysiol. 65, 188–202.
Simonyan, K., Saad, Z. S., Loucks, T. M., Poletto, C. J., and Ludlow, C. L. (2007). Functional neuroanatomy of human voluntary cough and sniff production. Neuroimage 37, 401–409. doi: 10.1016/j.neuroimage.2007.05.021
Soberaa, M., Siedleckaa, B., and Syczewskab, M. (2011). Posture control development in children aged 2–7 years old, based on the changes of repeatability of the stability indices. Neurosci. Lett. 491, 13–17. doi: 10.1016/j.neulet.2010.12.061
Stafford, R. E., Ashton-Miller, J. A., Sapsford, R., and Hodges, P. W. (2012). Activation of the striated urethral sphincter to maintain continence during dynamic tasks in healthy men. Neurourol. Urodyn. 31, 36–43. doi: 10.1002/nau.21178
Stapley, P. J., Pozzo, T., Cheron, G., and Grishin, A. (1999). Does the coordination between posture and movement during human whole-body reaching ensure center of mass stabilization? Exp. Brain Res. 129, 134–146. doi: 10.1007/s002210050944
Stapley, P., Pozzo, T., and Grishin, A. (1998). The role of anticipatory postural adjustments during whole body forward reaching movements. Neuroreport 9, 395–401. doi: 10.1097/00001756-199802160-00007
Takeuchi, H., Sekiguchi, A., Taki, Y., Yokoyama, S., Yomogida, Y., Komuro, N., et al. (2010). Training of working memory impacts structural connectivity. J. Neurosci. 30, 3297–3303. doi: 10.1523/JNEUROSCI.4611-09.2010
Tamnes, C. K., Østby, Y., Walhovd, K. B., Westlye, L. T., Due-Tønnessen, P., and Fjell, A. M. (2010a). Intellectual abilities and white matter microstructure in development: a diffusion tensor imaging study. Hum. Brain Mapp. 31, 1609–1625. doi: 10.1002/hbm.20962
Tamnes, C. K., Østby, Y., Walhovd, K. B., Westlye, L. T., Due-Tønnessen, P., and Fjell, A. M. (2010b). Neuroanatomical correlates of executive functions in children and adolescents: a magnetic resonance imaging (MRI) study of cortical thickness. Neuropsychologia 48, 2496–2508. doi: 10.1016/j.neuropsychologia.2010.04.024
Thind, P., Lose, G., Jørgensen, L., and Colstrup, H. (1990). Variations in urethral and bladder pressure during stress episodes in healthy women. Br. J. Urol. 66, 389–392. doi: 10.1111/j.1464-410x.1990.tb14960.x
Thüroff, J. W., Casper, F., and Heidler, H. (1987). Pelvic floor stress response: reflex contraction with pressure transmission to the urethra. Urol. Int. 42, 185–189. doi: 10.1007/978-3-642-72735-1_19
van der Kooi, J. B., van Wanroy, P. J., De Jonge, M. C., and Kornelis, J. A. (1984). Time separation between cough pulses in bladder, rectum and urethra in women. J. Urol. 132, 1275–1278. doi: 10.1016/s0022-5347(17)50122-6
Yakovlev, P. I., and Lecours, A. R. (1967). “The myelogenetic cycles of regional maturation of the brain,” in Regional Development of the Brain in Early Life, ed. A. Minkowski (Oxford, UK: Blackwell), 3–70.
Keywords: cough-anal reflex, intra-limb APAs, inter-limb APAs, common mechanism, cough, external anal sphincter
Citation: Cavallari P, Bolzoni F, Esposti R and Bruttini C (2017) Cough-Anal Reflex May Be the Expression of a Pre-Programmed Postural Action. Front. Hum. Neurosci. 11:475. doi: 10.3389/fnhum.2017.00475
Received: 08 June 2017; Accepted: 12 September 2017;
Published: 27 September 2017.
Edited by:Mikhail Lebedev, Duke University, United States
Reviewed by:Silvia Demoulin-Alexikova, Université de Lorraine, France
Michael Swash, Barts and The London School of Medicine and Dentistry, United Kingdom; University of Lisbon, Portugal
Copyright © 2017 Cavallari, Bolzoni, Esposti and Bruttini. 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) or licensor 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: Paolo Cavallari, firstname.lastname@example.org