Attenuation of acute restraint stress-induced depressive like behavior and hippocampal alterations with protocatechuic acid treatment in mice
Abstract
Protocatechuic acid ethyl ester (PCA), a phenolic compound, exhibits neuroprotective effects through improving endogenous antioxidant enzymatic and nonezymatic system. Based on the role of oxidative stress in modulating depressive disorders and the relationship between neuroprotective and antioxidant potential of PCA, we studied if its antidepressant like effect is associated by modulation of cerebral cortex and hippocampal antioxidant alterations. Acute restraint stress (ARS) is known to induce depressive like behavior by neuronal oxidative damage in mice. Swiss albino mice subjected to ARS exhibited an increased immobility time in forced swim test, elevated serum corticosterone and produced oxidative stress dependent alterations in cerebral cortex and hippocampus mainly increased thiobarbituric acid reactive substances and reduced catalase (CAT), superoxide dismutase (SOD) activity. Treatment with PCA was able to prevent stress induced immobility time in forced swim test without altering locomotor activity in mice. Further, PCA treatment attenuated the elevation of serum corticosterone, lipid peroxidation and restored enzymatic antioxidants in cerebral cortex and hippocampus in ARS mice. Altogether, the experimental findings demonstrate the notion that PCA exhibit antidepressant like activity might be related, at least in part, to its capability of modulating antioxidant defense system and oxidative damage induced by ARS in cerebral cortex and hippocampus in mice and thus maintain the pro-/anti-oxidative homeostasis.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Protocatechuic acid, which is part of quinoa composition, maintains pro-/antioxidant homeostasis in the cerebral cortex and hippocampus in mice under immobilization stress.
“The ability to maintain pro-/antioxidant homeostasis in the cerebral cortex and hippocampus in mice under immobilization stress has been demonstrated by protocatechuic acid, which is part of quinoa composition [39].”
From Anxiolytic and Antioxidant Effect of Phytoecdysteroids and Polyphenols from Chenopodium quinoa on an In Vivo Restraint Stress Model (2022) · cites this paper as [39]
Cites
Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction
Ohkawa, H., Ohishi, N., & Yagi, K. (1979) · Analytical Biochemistry · doi:10.1016/0003-2697(79)90738-3 · Cited by 29,460 · see citing works
Ellman, G. L. (1959) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(59)90090-6 · Cited by 26,824 · see citing works
Aebi, H. (1984) · Methods in Enzymology · doi:10.1016/s0076-6879(84)05016-3 · Cited by 25,696 · see citing works
Misra, H. P., & Fridovich, I. (1972) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)45228-9 · Cited by 9,097 · see citing works
Molecular Mechanisms of Depression: Perspectives on New Treatment Strategies
Lang, U. E., & Borgwardt, S. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350094 · Cited by 8,501 · see citing works
Behavioral despair in mice: a primary screening test for antidepressants.
Porsolt, R. D., Bertin, A., & Jalfre, M. (1977) · PubMed · Cited by 3,275 · see citing works
Stress and disorders of the stress system
Chrousos, G. P. (2009) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2009.106 · Cited by 3,215 · see citing works
Clinical and Biochemical Manifestations of Depression
Gold, P. W., Goodwin, F. K., & Chrousos, G. P. (1988) · New England Journal of Medicine · doi:10.1056/nejm198808183190706 · Cited by 1,057 · see citing works
McKinnon, M. C., Yucel, K., Nazarov, A., & MacQueen, G. M. (2009) · Journal of Psychiatry and Neuroscience · doi:10.1139/jpn.0905 · Cited by 742 · see citing works
Life stressors as risk factors in depression.
Mazure, C. M. (1998) · Clinical Psychology: Science and Practice · doi:10.1111/j.1468-2850.1998.tb00151.x · Cited by 535 · see citing works
Sarandol, A., Sarandol, E., Eker, S. S., Erdinc, S., Vatansever, E., & Kirli, S. (2007) · Human Psychopharmacology: Clinical and Experimental · doi:10.1002/hup.829 · Cited by 486 · see citing works
Morris, M. C., Compas, B. E., & Garber, J. (2012) · Clinical Psychology Review · doi:10.1016/j.cpr.2012.02.002 · Cited by 466 · see citing works
Stress and depression: possible links to neuron death in the hippocampus
Lee, A. L., Ogle, W. O., & Sapolsky, R. M. (2002) · Bipolar Disorders · doi:10.1034/j.1399-5618.2002.01144.x · Cited by 462 · see citing works
Restraint stress in biobehavioral research: Recent developments
Buynitsky, T., & Mostofsky, D. I. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.05.004 · Cited by 426 · see citing works
Chronic and acute stress and the prediction of major depression in women
Hammen, C., Kim, E. Y., Eberhart, N. K., & Brennan, P. A. (2009) · Depression and Anxiety · doi:10.1002/da.20571 · Cited by 347 · see citing works
What's wrong with my mouse model?
Kalueff, A. V., Wheaton, M., & Murphy, D. L. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.01.023 · Cited by 285 · see citing works
Decreased glutathione transferase activity in brain and ventricular fluid in Alzheimer's disease
Lovell, M. A., Xie, C., & Markesbery, W. R. (1998) · Neurology · doi:10.1212/wnl.51.6.1562 · Cited by 275 · see citing works
Pacheco-Palencia, L. A., Mertens‐Talcott, S. U., & Talcott, S. T. (2008) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf800161u · Cited by 239 · see citing works
Shi, G., An, L., Jiang, B., Guan, S., & Bao, Y. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.02.057 · Cited by 199 · see citing works
Repeated Restraint Stress Induces Oxidative Damage in Rat Hippocampus
Fontella, F. U., Siqueira, I. R., de Vasconcellos, A. P. S., Tabajara, Â. S., Netto, C. A., & Dalmaz, C. (2005) · Neurochemical Research · doi:10.1007/s11064-004-9691-6 · Cited by 195 · see citing works
In vivo antioxidant status: A putative target of antidepressant action
Zafir, A., Ara, A., & Banu, N. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2008.11.010 · Cited by 183 · see citing works
Zhang, Z., Li, G., Szeto, S. S. W., Chong, C. M., Quan, Q., Huang, C., Cui, W., Guo, B., Wang, Y., Han, Y., et al. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.02.030 · Cited by 169 · see citing works
Suresh Ramnath, N. A. I. K., Thakare, V. N., & Patil, S. R. (2010) · Experimental and Toxicologic Pathology · doi:10.1016/j.etp.2010.03.001 · Cited by 168 · see citing works
Self-citationCapra, J. C., Cunha, M. P., Machado, D. G., Zomkowski, A. D. E., Mendes, B. G., Santos, A. R. S., Pizzolatti, M. G., & Rodrigues, A. L. S. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.06.043 · Cited by 164 · see citing works
Antioxidant potential of fluoxetine in comparison to Curcuma longa in restraint-stressed rats
Zafir, A., & Banu, N. (2007) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.05.062 · Cited by 156 · see citing works
Protocatechuic acid from Alpinia oxyphylla against MPP+-induced neurotoxicity in PC12 cells
An, L. J., Guan, S., Shi, G., et al. (2005) · Food and Chemical Toxicology · doi:10.1016/j.fct.2005.08.017 · Cited by 145 · see citing works
Guan, S., Bao, Y., Jiang, B. Q., et al. (2006) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2006.03.065 · Cited by 142 · see citing works
Do antioxidants impair signaling by reactive oxygen species and lipid oxidation products?
Niki, E. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.09.025 · Cited by 138 · see citing works
Effect of Perinatal Lead Exposure on Rat Behaviour in Open‐Field and Two‐Wky Avoidance Tasks
Rodrigues, A. L. S., da Rocha, J. B. T., Mello, C. F., & Souza, D. O. (1996) · Pharmacology & Toxicology · doi:10.1111/j.1600-0773.1996.tb00259.x · Cited by 136 · see citing works
A review on animal models for screening potential anti-stress agents
Jaggi, A. S., Bhatia, N., Kumar, N., Singh, N., Anand, P., & Dhawan, R. K. (2011) · Neurological Sciences · doi:10.1007/s10072-011-0770-6 · Cited by 134 · see citing works
Lee, B., Shim, I., Lee, H., Yang, Y. D., & Hahm, D. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.01.076 · Cited by 109 · see citing works
Freitas, A. E., Bettio, L. E. B., Neis, V. B., Santos, D. B., Ribeiro, C. M., da Rosa, P. B., Farina, M., & Rodrigues, A. L. S. (2013) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2013.12.012 · Cited by 108 · see citing works
Christiansen, S. H., Olesen, M. V., Wörtwein, G., & Woldbye, D. P. D. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.08.044 · Cited by 103 · see citing works
Burri, A. V., Maercker, A. R. A., Krammer, S., & Simmen‐Janevska, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057826 · Cited by 97 · see citing works
Melatonin treatment mimics the antidepressant action in chronic corticosterone‐treated mice
Crupi, R., Mazzon, E., Marino, A., Spada, G. L., Bramanti, P., Cuzzocrea, S., & Spina, E. (2010) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2010.00775.x · Cited by 95 · see citing works
Budni, J., Zomkowski, A. D. E., Engel, D. F., Santos, D. B., dos Santos, A. A., Moretti, M., Valvassori, S. S., Ornell, F. R., Quevedo, J., Farina, M., et al. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.10.024 · Cited by 94 · see citing works
Protective Effects of Ascorbic Acid on Behavior and Oxidative Status of Restraint-Stressed Mice
Moretti, M., Budni, J., Santos, D. B., Antunes, A. A., Daufenbach, J. F., Manosso, L. M., Farina, M., & Rodrigues, A. L. S. (2012) · Journal of Molecular Neuroscience · doi:10.1007/s12031-012-9892-4 · Cited by 92 · see citing works
Hibiscus protocatechuic acid inhibits lipopolysaccharide-induced rat hepatic damage
W.-L., L., Y.-J., H., F.-P., C., C.-J., W., M.-T., C., & Tseng, T. (2003) · Archives of Toxicology · doi:10.1007/s00204-002-0404-0 · Cited by 91 · see citing works
Zhang, Y., Wu, L., Zhang, Q., et al. (2011) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2011.04.023 · Cited by 88 · see citing works
Jin, P., Yu, H.-L., Tian-Lan, Zhang, F., & Quan, Z. (2015) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2015.04.001 · Cited by 68 · see citing works
Piperine reverses the effects of corticosterone on behavior and hippocampal BDNF expression in mice
Mao, Q., Huang, Z., Zhong, X., Xian, Y., & Ip, S. (2014) · Neurochemistry International · doi:10.1016/j.neuint.2014.04.017 · Cited by 65 · see citing works
Thakare, V. N., Dhakane, V. D., & Patel, B. M. (2016) · Pharmacological Reports · doi:10.1016/j.pharep.2016.06.002 · Cited by 63 · see citing works
Self-citationZhao, Y., Xie, W., Dai, J., Wang, Z., & Huang, Y. (2009) · Brain Research · doi:10.1016/j.brainres.2008.12.083 · Cited by 61 · see citing works
Bettio, L. E. B., Freitas, A. E., Neis, V. B., Santos, D. B., Ribeiro, C. M., da Rosa, P. B., Farina, M., & Rodrigues, A. L. S. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2014.10.002 · Cited by 59 · see citing works
Kumar, A., & Goyal, R. (2008) · Journal of Medicinal Food · doi:10.1089/jmf.2006.0207 · Cited by 58 · see citing works
Jindal, A., Mahesh, R., & Bhatt, S. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.01.020 · Cited by 57 · see citing works
Kobayashi, N., Machida, T., Takahashi, T., Takatsu, H., Shinkai, T., Abe, K., & Urano, S. (2009) · Journal of Clinical Biochemistry and Nutrition · doi:10.3164/jcbn.09-33 · Cited by 57 · see citing works
Muley, M. M., Thakare, V. N., Patil, R. R., et al. (2013) · Life Sciences · doi:10.1016/j.lfs.2013.05.020 · Cited by 57 · see citing works
Self-citationMuley, M. M., Thakare, V. N., Patil, R. R., et al. (2012) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2012.05.004 · Cited by 44 · see citing works
Self-citationOstadhadi, S., Khan, M. I., Norouzi‐Javidan, A., & Dehpour, A. R. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.04.026 · Cited by 43 · see citing works
Antistress properties of antidepressant drugs and their clinical implications
Calabrese, F., Molteni, R., & Riva, M. A. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.05.007 · Cited by 41 · see citing works
Monoamine Oxidase and Dopamine β-Hydroxylase Inhibitors from the Fruits of Gardenia jasminoides
Kim, J.-H., Kim, G.-H., & Hwang, K.-H. (2012) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2012.20.2.214 · Cited by 41 · see citing works
Kumar, A., Garg, R., Gaur, V., & Kumar, P. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.10.004 · Cited by 35 · see citing works
Rosa, J. M., Dafré, A. L., & Rodrigues, A. L. S. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.07.009 · Cited by 32 · see citing works
Enache, M., Waes, V. V., Vinner, É., Lhermitte, M., Maccari, S., & Darnaudéry, M. (2007) · Brain Research · doi:10.1016/j.brainres.2007.11.031 · Cited by 30 · see citing works
Balk, R. D. S., Bridi, J. C., Portella, R. D. L., de Carvalho, N. R., Dobrachinski, F., da Silva, M. H., Amaral, G. P., Dias, G. R. M., Barbosa, N. V., & Soares, F. A. A. (2010) · Neurochemical Research · doi:10.1007/s11064-010-0240-1 · Cited by 27 · see citing works
Potential Targets for the Development of Novel Antidepressants: Future Perspectives
Thakare, V. N., & Patel, B. M. (2015) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527313666140806121648 · Cited by 11 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Sidorova, Y. S., Shipelin, V. A., Petrov, N. A., Zorin, S. N., & Mazo, V. K. (2022) · Molecules · doi:10.3390/molecules27249003 · Cited by 11 · see citing works
- Authors
- Thakare, V. N., Dhakane, V. D., & Patel, B. M.
- Affiliations
- Nirma University (IN)
- Corresponding author
- Patel, Bhoomika M.
- Venue
- Metabolic Brain Disease
- Published
- 2016-10-26
- Volume
- 32
- Issue
- 2
- Pages
- 401-413
- ISSN
- 0885-7490 (ISSN-L)
- 1573-7365
- OpenAlex
- W2540823011
- Cited by
- 49
- References
- 58
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 6 · 2023: 7 · 2022: 7 · 2021: 5 · 2020: 9 · 2019: 4 · 2018: 4 · 2017: 2
- FWCI
- 2.70
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Metabolic Brain Disease (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Medicinal Plants and Bioactive Compounds
- Keywords
- protocatechuic acid, acute restraint stress, depression-like behavior, hippocampus, cerebral cortex, oxidative stress, antioxidant enzymes, catalase, superoxide dismutase, lipid peroxidation, corticosterone, forced swim test, antidepressant effects, neuroprotection
- MeSH terms
- Animals, Antioxidants, Anxiety, Atrophy, Corticosterone, Depression, Female, Hippocampus, Male, Motor Activity, Restraint, Physical, Stress, Psychological, Lipid Peroxidation, Oxidative Stress, Neuroprotective Agents, Mice, Hydroxybenzoates
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review