UTILITIES AND LIMITATIONS OF CURRENT ANIMAL MODELS OF DEPRESSION

Authors

  • Andy Ramjattan Department of Paraclinical Sciences, Faculty of Medical Sciences, The University of the West Indies, St. Augustine Campus, Trinidad and Tobago.
  • Pinto Pereira Lexley M Department of Paraclinical Sciences, Faculty of Medical Sciences, The University of the West Indies, St. Augustine Campus, Trinidad and Tobago.
  • Sameer Dhingra School of Pharmacy, Faculty of Medical Sciences, The University of the West Indies, St. Augustine Campus, Trinidad and Tobago http://orcid.org/0000-0003-2537-8889

DOI:

https://doi.org/10.22159/ajpcr.2017.v10i12.20811

Keywords:

Animal models, Depression, Behavioral models, Chemical models, Forced swim test, Tail suspension test

Abstract

 

 Depression is one of the most debilitating medical conditions in the world today, yet its etiologies remain imprecise, and current treatments are not wholly helpful. Depression is more than just a feeling of sadness. Depression can affect the daily routine of an individual disrupting work, play, and overall ability to concentrate. People with depression usually experience a lack of interest and enjoyment in daily activities, notable weight loss or gain, sleeplessness or excessive sleeping, lack of energy, inability to concentrate, feelings of worthlessness or shame, and recurrent thoughts of suicide (diagnostic and statistical manual-V). It is projected to be the second leading cause of disability worldwide by 2020. It is estimated that depression currently affects 350 million people from around the world. There are a number of drugs of different pharmacological classes being used in the treatment of clinical depression. Animal models are indispensable tools in the search to identify new antidepressant drugs and to provide insights into the neuropathology that underlies the idiopathic disease state of depression. Animal models of depression can be used for a variety of purposes, including use as a tool for investigating aspects of the neurobiology and pathophysiology of depression, as an experimental model for studying the mechanism of action of antidepressant drugs and for screening antidepressant activity. None of existing animal models currently fulfil the existing criteria for an ideal animal model, and therefore, demands an insight view of the existing models of depression. This article attempts to review the most widely used animal models and highlights their important features with respect to different pharmacological classes of antidepressant drugs.

Downloads

Download data is not yet available.

Author Biographies

Andy Ramjattan, Department of Paraclinical Sciences, Faculty of Medical Sciences, The University of the West Indies, St. Augustine Campus, Trinidad and Tobago.

Department of Paraclinical Sciences

Pinto Pereira Lexley M, Department of Paraclinical Sciences, Faculty of Medical Sciences, The University of the West Indies, St. Augustine Campus, Trinidad and Tobago.

Professor Emeritus, Pharmacology Unit

Sameer Dhingra, School of Pharmacy, Faculty of Medical Sciences, The University of the West Indies, St. Augustine Campus, Trinidad and Tobago

Lecturer, School of Pharmacy

References

Rueger S, Malecki C, Pyun Y, Aycock C, Coyle S. A meta-analytical review of the association between perceived social support and depression in childhood and adolescence. Psychol Bull 2016;142(10):1017-67.

U.S. Department of Health and Human Services. National Institute of Mental Health NIH Publication No. 15-3561; 2015.

Chisholm D, Sweeny K, Sheehan P, Rasmussen B, Smit F, Cuijpers P, et al. Scaling-up treatment of depression and anxiety: A global return on investment analysis. Lancet Psychiatry 2016;3(5):415-24.

Chilvers C, Dewey M, Fielding K, Gretton V, Miller P, Palmer B, et al. Antidepressant drugs and generic counselling for treatment of major depression in primary care: Randomised trial with patient preference arms. BMJ 2001;322(7289):772-5.

Litwack G, Duman C. Vitamins and Hormones. Vol. 82. New Haven, Connecticut, USA: Elsevier Inc.; 2010. p. 1-270.

Holsboer F. The corticosteroid receptor hypothesis of depression. Neuropsychopharmacology 2000;23(5):477-501.

Wells B. Pharmacotherapy Handbook. Vol.71. New York: McGraw-Hill; 2012. p. 873-92.

McGonigle P, Ruggeri B. Animal models of human disease: Challenges in enabling translation. Biochem Pharmacol 2014;87(1):162-71.

Porsolt RD, Bertin A, Jalfre M. Behavioral despair in mice: A primary screening test for antidepressants. Arch Int Pharmacodyn Ther 1977;229(2):327-36.

Cryan JF, Valentino RJ, Lucki I. Assessing substrates underlying the behavioral effects of antidepressants using the modified rat forced swimming test. Neurosci Biobehav Rev 2005;29(4-5):547-69.

Steru L, Chermat R, Thierry B, Simon P. The tail suspension test: A new method for screening antidepressants in mice. Psychopharmacology (Berl) 1985;85(3):367-70.

Liu X, Peprah D, Howard K, Gershenfeld HK. Tail-suspension induced hyperthermia: A new measure of stress reactivity. J Psychiatr Res 2003;37(3):249-59.

Selingman ME, Rosellini RA, Kozack MJ. Learned helplessness in rate: Time course, immunization and reversibility. J Comp Physiol Psychol 1978;88(2):542-7.

Milind P, Dhingra S. A review on animal models of depression. Asian J Bio Sci 2010;5(1):151-63.

Santosh P, Venugopl R, Nilakash AS, Kunjbihari S, Mangala L. Antidepressant activity of methanolic extract of Passiflora foetida leaves in mice. Int J Pharm Pharm Sci 2011;3(1):112-5.

Song C, Leonard B. The olfactory bulbectomised rat as a model of depression. Neurosci Biobehav Rev 2005;29(4):627-47.

Kashmira G, Mayuri L. Rodent antidepressant models in neuropsychopharmacology: A laboratory prospective. Int J Res Pharm Sci 2012;4(1):21-43.

Heim C, Nemeroff CB. The role of childhood trauma in the neurobiology of mood and anxiety disorders: Preclinical and clinical studies. Biol Psychiatry 2009;49:1023-39.

Berton O, McClung CA, Dileone RJ, Krishnan V, Renthal W, Russo SJ, et al. Essential role of BDNF in the mesolimbic dopamine pathway in social defeat stress. Science 2006;311(5762):864-8.

Meerlo P, Overkamp GJ, Daan S, Van Den Hoofdakker RH, Koolhaas JM. Changes in behaviour and body weight following a single or double social defeat in rats. Stress 1996;1(1):21-32.

Bohus B, Koolhaas JM, Heijnen CJ, Boer O. Immunological responses to social stress: Dependence on social environment and coping abilities. Neuropsychobiology 1993;28(1-2):95-9.

Buwalda B, de Boer SF, Schmidt ED, Felszeghy K, Nyakas C, Sgoifo A, et al. Long-lasting deficient dexamethasone suppression of hypothalamic-pituitary-adrenocortical activation following peripheral CRF challenge in socially defeated rats. J Neuroendocrinol 1999;11(7):513-20.

Krishnan V, Han MH, Graham DL, Berton O, Renthal W, Russo SJ, et al. Molecular adaptations underlying susceptibility and resistance to social defeat in brain reward regions. Cell 2007;131(2):391-404.

Willner P. Chronic mild stress (CMS) revisited: Consistency and behavioural-neurobiological concordance in the effects of CMS. Neuropsychobiology 2005;52(2):90-110.

Broekkamp C. Predictive validity and the robustness criterion for animal models. Psychopharmacology 1997;134(4):341-3.

Kong H, Sha LL, Fan Y, Xiao M, Ding JH, Wu J, et al. Requirement

of AQP4 for antidepressive efficiency of fluoxetine: Implication in adult hippocampal neurogenesis. Neuropsychopharmacology 2009;34(5):1263-76.

27. Pryce CR, Rüedi-Bettschen D, Dettling AC, Weston A, Russig H, Ferger B, et al. Long-term effects of early-life environmental manipulations in rodents and primates: Potential animal models in depression research. Neurosci Biobehav Rev 2005;29(4-5):649-74.

28. Heim C, Newport DJ, Bonsall R, Miller AH, Nemeroff CB. Altered pituitry-adrenal axis responses to provocative challenge tests in adult survivors of childhood abuse. Am J Psychiatry 2003;1(3):282-9.

29. Kendler KS, Gardner CO, Prescott CA. Toward a comprehensive developmental model for major depression in women. Am J Psychiatry 2002;159(7):1133-45.

30. Zhang TY, Bagot R, Parent C, Nesbitt C, Bredy TW, Caldji C, et al. Maternal programming of defensive responses through sustained effects on gene expression. Biol Psychiatry 2006;73(1):72-89.

31. Ladd CO, Huot RL, Thrivikraman KV, Nemeroff CB, Meaney MJ, Plotsky PM. Long-term behavioral and neuroendocrine adaptations to adverse early experience. Prog Brain Res 2000;122:81-103.

32. Levine S. Infantile experience and resistance to physiological stress. Science 1957;126(3270):405.

33. Alonso SJ, Arevalo R, Afonso D, Rodríguez M. Effects of maternal stress during pregnancy on forced swimming test behavior of the offspring. Physiol Behav 1991;50(3):511-7.

34. Maccari S, Darnaudery M, Morley-Fletcher S, Zuena AR, Cinque C, Van Reeth O. Prenatal stress and long-term consequences: Implications of glucocorticoid hormones. Neurosci Biobehav Rev 2003;27(1-2):119-27.

35. McCormick CM, Smythe JW, Sharma S, Meaney MJ. Sex-specific effects of prenatal stress on hypothalamic-pituitary-adrenal responses to stress and brain glucocorticoid receptor density in adult rats. Brain Res Dev Brain Res 1995;84(1):55-61.

36. Morilak DA, Frazer A. Antidepressants and brain monoaminergic systems: A dimensional approach to understanding their behavioural effects in depression and anxiety disorders. Int J Neuropsychopharmacol 2004;7(2):193-218.

37. Morley-Fletcher S, Rea M, Maccari S, Laviola G. Environmental enrichment during adolescence reverses the effects of prenatal stress on play behaviour and HPA axis reactivity in rats. Eur J Neurosci 2003;18(12):3367-74.

38. Morley-Fletcher S, Darnaudéry M, Mocaer E, Froger N, Lanfumey L, Laviola G, et al. Chronic treatment with imipramine reverses immobility behaviour, hippocampal corticosteroid receptors and cortical 5-HT(1A) receptor mRNA in prenatally stressed rats. Neuropharmacology 2004;47(6):841-7.

39. Secoli SR, Teixeira NA. Chronic prenatal stress affects development and behavioral depression in rats. Stress 1998;2(4):273-80.

40. Smith JW, Seckl JR, Evans AT, Costall B, Smythe JW. Gestational stress induces post-partum depression-like behaviour and alters maternal care in rats. Psychoneuroendocrinology 2004;29(2):227-44.

41. Weinstock M. Does prenatal stress impair coping and regulation of hypothalamic-pituitary-adrenal axis? Neurosci Biobehav Rev 1997;21(1):1-10.

42. Weinstock M, Matlina E, Maor GI, Rosen H, McEwen BS. Prenatal stress selectively alters the reactivity of the hypothalamic-pituitary adrenal system in the female rat. Brain Res 1992;595(2):195-200.

43. Ridder S, Chourbaji S, Hellweg R, Urani A, Zacher C, Schmid W, et al. Mice with genetically altered glucocorticoid receptor expression show altered sensitivity for stress-induced depressive reactions. J Neurosci 2005;25(26):6243-50.

44. Aguilera G. Corticotropin releasing hormone, receptor regulation and the stress response. Trends Endocrinol Metab 1998;9(8):329-36.

45. Nielsen CK, Arnt J, Sánchez C. Intracranial self-stimulation and sucrose intake differ as hedonic measures following chronic mild stress: Interstrain and interindividual differences. Behav Brain Res 2000;107(1-2):21-33.

46. Leith NJ, Barrett RJ. Effects of chronic amphetamine or reserpine on self-stimulation responding: Animal model of depression? Psychopharmacology (Berl) 1980;72(1):9-15.

47. Yadav YC, Jain A, Deb L. A review: Neuropharmacological screening techniques for pharmaceuticals. Int J Pharm Pharm Sci 2010;2(2):10-4.

48. Cassens GP, Actor C, Kling M, Schildkraut JJ. Amphetamine withdrawal effects threshold of intracranial self-stimulation. Psychopharmacolgy 1981;73(4):318-22.

49. Samuels B, Leonardo E, Gadient R, Williams A, Zhou J, David DJ, et al. Modeling treatment-resistant depression. Neuropharmacology 2011;61(3):408-13.

50. Hibicke M. Development and Evaluation of an Adolescent Chronic Restraint Stress (ACRS) Protocol to Model Adult Depression in Female Rats. Diss. Mercer University; 2017.

Published

01-12-2017

How to Cite

Ramjattan, A., P. Pereira Lexley M, and S. Dhingra. “UTILITIES AND LIMITATIONS OF CURRENT ANIMAL MODELS OF DEPRESSION”. Asian Journal of Pharmaceutical and Clinical Research, vol. 10, no. 12, Dec. 2017, pp. 11-16, doi:10.22159/ajpcr.2017.v10i12.20811.

Issue

Section

Review Article(s)