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OPINION article

Front. Physiol., 17 October 2013
Sec. Membrane Physiology and Membrane Biophysics

Nitric oxide and membrane lipid peroxidation in photosynthetic and non-photosynthetic organisms under several stress conditions

  • Physical Chemistry, School of Pharmacy and Biochemistry, Institute of Biochemistry and Molecular Medicine, University of Buenos Aires-CONICET, Buenos Aires, Argentina


Oxidative damage to lipids was characterized in terms of the nature of the oxidant, the type of lipid, and the severity of the oxidation (Simontacchi et al., 2011). Even though malondialdehyde detection with the thiobarbituric acid reactive substances test (TBARS) is the most currently used assay for the determination of lipid oxidation, it is unspecific since the reaction can be reproduced by other biological compounds (Simontacchi et al., 2011). On the other hand, electron paramagnetic resonance (EPR) spectroscopy showed the capacity of detecting the presence of the lipid radicals (LR) formed during peroxidation, by yielding unique and stable products with spin traps (Malanga and Puntarulo, 2012). Nitric oxide (NO) is recognized both, as a signaling molecule that regulates many enzyme activities, but as a toxic agent as well. It has been found that NO is able to protect animal and plant cell types from oxidative damage resulting from superoxide (O2), hydrogen peroxide (H2O2) and alkyl peroxides by acting as a terminator of free radical chain reactions (Wink et al., 1995, 1996; Yalowich et al., 1999; Beligni and Lamattina, 2002; Sharpe et al., 2003). Reactive oxygen species (ROS) and reactive nitrogen species (RNS) interact through the reaction of O2 with NO, to generate peroxynitrite (ONOO) at a rate close to diffusion. ONOO acts as both, a nitrating agent and a powerful oxidant capable of modifying proteins (formation of nitrotyrosine), lipids (lipid oxidation, lipid nitration), and nucleic acids (DNA oxidation and DNA nitration) (Gisone et al., 2004).

The purpose of this commentary is to point out that NO complex interactions with other cellular components lead to a wide range of effects depending on the biological system under study and the oxidative stress condition.

Lipid Peroxidation and NO in Photosynthetic Organisms

In cultures of the green algae Chlorella vulgaris no significant changes were observed in either of the parameters showed in Table 1, in the stationary phase as compared to the log phase of growth. However, Qian et al. (2009) demonstrated in Chlorella vulgaris that, depending on its concentration, NO increased the activity of antioxidant enzymes to protect against the oxidative damage caused by herbicide stress. Data from Simontachi et al. (2004) showed that the NO steady state concentration in homogenates from sorghum embryonic axes reached a maximum at 24–30 h after the starting of imbibition, in coincidence with the initiation of an active germination. The generation of LR in sorghum axes was drastically increased at 36 h of imbibition from non-detectable values at 24 h, coincidentally with the significant decline in the content of cellular NO (Table 1).


Table 1. Nitric oxide and lipid peroxidation under stress conditions in photosynthetic and non-photosynthetic organisms.

To analyze the role of NO during senescence, Jasid et al. (2009) sprayed daily soybean cotyledons with an NO donor solution (sodium nitroprusside, SNP), from day 5 to 25. Differently from naturally senescent cotyledons, where NO content reached a maximum at day 10 of seedling development and declined, in SNP-treated cotyledons NO content was higher, and remained unchanged from day 10 to 25 after germination, as compared to control values. While naturally senescent cotyledons experimented no change in the content of LR during the studied period, SNP-treated cotyledons showed a decrease as time progressed (Table 1).

Shi et al. (2005) suggested that the protective effect of NO on the oxidative damage of thylakoid membrane proteins in Phaseolus vulgaris beans under UV-B radiation may be mediated by increasing the level of expression of genes encoding ROS-scavenging enzymes. Moreover, Jasid et al. (2006) showed that isolated chloroplasts from soybean leaves exposed to 2 μM NO for 30 min, decreased the rate of LR generation (Table 1). Also, Jasid et al. (2008) reported that axes from sorghum seeds incubated 24 h in the presence of SNP, showed a significantly higher NO content as compared to control axes, and LR content evaluated in the microsomal fractions was significantly lower, as compared to control membranes (Table 1).

Lipid Peroxidation and NO in Non-Photosynthetic Organisms

Data in Table 1 show that seasonality affects oxidative metabolism in digestive glands (DG) from Nacella magellanica limpets isolated from the Beagle Channel, Tierra del Fuego, Argentina. A significant increase in both LR and NO content in summer, as compared to winter, was reported (Malanga et al., 2007). However, studies on toxicological effects of Fe exposure under laboratory conditions showed that significant increases in lipid peroxidation were temporarily associated to decreases in NO content in DG from the bivalve Mya arenaria after 17 days of treatment (González et al., 2010) (Table 1).

In vivo γ irradiation of rat fetuses did not significantly affect neither the content of LR nor the content of TBARS in the brain up to 2 h post-irradiation (pi). However, 4 h after the exposure, a significant increase in the TBARS content was measured. These results are consistent with the hypothesis that changes could be produced in the brain at the early stages after exposure to γ radiation to limit free radical-dependent damage, since increased lipid peroxidation was only detected after 4 h pi. Gisone et al. (2003) showed that total NO synthase activity was increased after 30 and 60 min pi, and returned to control values after 2 h pi, and accordingly NO content was significantly increased (Table 1).

Galleano and Puntarulo (1992) showed that liver homogenates from Fe-dextran overloaded male Wistar rats showed a significant increase in TBARS 6 h post-injection, as compared to control rats (Table 1). Later, Galleano et al. (2001) pointed out that the significant increase in NO, assayed as DETC2–Fe–NO adducts 5 h after Fe administration could be an artifact due to the excess of Fe during the measurement. Recently, Rousseau et al. (2011) showed that one of the molecular footprints left by the reactions of ROS with biomolecules, the level of protein 3-nitrotyrosines, was not increased by Fe-dextran administration, suggesting that Fe overload in liver did not change NO cellular content (Table 1).

Concluding Remarks

The results summarized here implied the existence of a very complex regulatory interplay between NO and ROS. The multiple effects of NO on the process of lipid peroxidation imply that the net result will depend on the balance of competing factors. The rate and location of NO formation, and also the rate of formation of O2, or other mitigating factors, will all contribute to the degree and the nature of the effect on lipid oxidation in a particular system. Detailed analysis of the molecular mechanisms in each condition is required. In this regard, no yet deeply studied NO reactions, such as NO binding to Fe and endogenous thiols and other nitrosyl–Fe complexes that seems to favor Fe release from the cell avoiding its accumulation, could reveal to be a key factor in NO cellular interactions and should be further characterized.


This study was supported by grants from the University of Buenos Aires, ANPCyT and CONICET to Susana Puntarulo. Susana Puntarulo, Gabriela Malanga, and Andrea Galatro are career investigator from CONICET, and Paula M. González and Natacha Piloni are fellows from CONICET.


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Keywords: nitric oxide, lipid peroxidation, photosynthetic organisms, animals, oxidative stress conditions

Citation: Galatro A, González PM, Malanga G, Robello E, Piloni NE and Puntarulo S (2013) Nitric oxide and membrane lipid peroxidation in photosynthetic and non-photosynthetic organisms under several stress conditions. Front. Physiol. 4:276. doi: 10.3389/fphys.2013.00276

Received: 15 July 2013; Accepted: 13 September 2013;
Published online: 17 October 2013.

Edited by:

Angel Catala, Universidad Nacional de La Plata, Argentina

Reviewed by:

Alexi Alekov, Medizinische Hochschule Hannover, Germany

Copyright © 2013 Galatro, González, Malanga, Robello, Piloni and Puntarulo. 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.