Genetic modulator of stress resilience and blood pressure regulation: insights from polymorphic variation

Authors

  • Bandana Kumari Department of Biochemistry, AIIMS Patna, Bihar, India

DOI:

https://doi.org/10.18203/2320-6012.ijrms20253744

Keywords:

Chronic stress, Haplotypes, Normotension, Neuropeptide Y, Polymorphism

Abstract

Neuropeptide Y (NPY) is a remarkably conserved neuropeptide distributed throughout the central and peripheral nervous systems, where it exerts broad influence over stress regulation and cardiovascular stability. While chronic stress typically contributes to increased blood pressure, a subset of individuals maintain normal levels despite similar stress exposure, suggesting the involvement of protective genetic factors within the NPY pathway. Variations in the NPY gene, particularly functional promoter polymorphisms such as rs16147 C>T and related haplotypes, appear to shape individual differences in stress responsiveness, sympathetic activation and emotional resilience. High-expression alleles are generally linked with reduced norepinephrine release, lower blood pressure and greater psychological stability under stress, whereas low-expression variants tend to enhance sympathetic tone and heighten vulnerability to anxiety and stress-related hypertension. Experimental studies reinforce the concept of NPY as a central sympathoinhibitory regulator, acting mainly through presynaptic Y₂ receptors within autonomic control centers. Recognizing these genetic influences offers valuable insight into why stress affects individuals so differently and opens new avenues for precision medicine. Genotypic profiling may ultimately aid in tailoring interventions for hypertension, anxiety and post-traumatic stress disorder. Moreover, pharmacological strategies targeting the NPY system such as Y₂ receptor agonists or agents that modulate epigenetic regulation, represents promising directions for future therapy. Continued longitudinal and translational research is essential to confirm causal mechanisms and to establish NPY as a clinically useful biomarker and therapeutic target in stress-related cardiovascular and neuropsychiatric disorders.

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References

Chrousos GP: Stress and disorders of the stress system. Nat Rev Endocrinol. 2009;5:374-81.

McEwen BS, Morrison JH: The brain on stress: vulnerability and plasticity of the prefrontal cortex over the life course. Neuron. 2013;23:16-29.

Heilig M: The NPY system in stress, anxiety and depression. Neuropeptides. 2004, 38:213-24.

Zukowska-Grojec Z. Neuropeptide Y. A novel sympathetic stress hormone and more. Ann New York Acad Sci. 1995;771:219-33.

Zhou Z, Zhu G, Hariri AR, Enoch MA, Scott D, Sinha R, et.al. Genetic variation in human NPY expression affects stress response and emotion. Nature. 2008;452(7190):997-1001.

Mickey BJ, Zhou Z, Heitzeg MM, Heinz E, Hodgkinson CA, Hsu DT, et al. Emotion processing, major depression and functional genetic variation of neuropeptide Y. Arch Gen Psych. 2011;68(2):158-66.

Tatemoto K, Carlquist M, Mutt V. Neuropeptide Y—a novel brain peptide with structural similarities to peptide YY and pancreatic polypeptide. Nature. 1982;296:659-60.

Michel MC, Beck-Sickinger A, Cox H, Doods HN, Herzog H, Larhammar DA, et al. XVI. International Union of Pharmacology recommendations for the nomenclature of neuropeptide Y, peptide YY and pancreatic polypeptide receptors. Pharm Rev. 1998;50(1):143-50.

Kask A, Kivastik T, Rägo L, Harro J. Neuropeptide Y Y1 receptor antagonist BIBP3226 produces conditioned place aversion in rats. Progress in neuro-psychopharmacology. Biol Psyc. 1999;23(4):705-11.

Parker RM, Herzog H: Regional distribution of Y-receptor subtype mRNAs in rat brain. Eur J Neurosci. 1999;11:1431-48.

Gerald C, Walker MW, Criscione L, Gustafson EL, Batzl-Hartmann C, Smith KE, et al. A receptor subtype involved in neuropeptide-Y-induced food intake. Nature. 1996;382(6587):168-71.

Tasan RO, Verma D, Wood J, Lach G, Hörmer B, de Lima TC, et al. The role of Neuropeptide Y in fear conditioning and extinction. Neuropeptides. 2016;55:111-26.

Baraban SC: Neuropeptide Y and limbic seizures. Rev Neurosci. 2002;13:85-94.

Lundberg JM, Tatemoto K: Pancreatic polypeptide family (APP, PYY, NPY) in relation to sympathetic nerves and adrenal medulla: functional and structural aspects. Ann NY Acad Sci. 1987;512:48-62.

Zukowska-Grojec Z, Karwatowska-Prokopczuk E, Rose W, Rone J, Movafagh S, Ji H, et al. Neuropeptide Y: a novel angiogenic factor from the sympathetic nerves and endothelium. Circulation research. 1998;83(2):187-95.

Mentlein R, Dahms P, Grandt D, Krüger R: Proteolytic processing of neuropeptide Y and peptide YY by dipeptidyl peptidase IV. Regul Pept. 1993;49:133-44.

Tuor UI, Kelly PA, Edvinsson L, McCulloch J. Neuropeptide Y and the cerebral circulation. Journal of Cerebral Blood Flow & Metabolism. 1990;10(5):591-601.

Thorsell A, Mathé AA. Neuropeptide Y in alcohol addiction and affective disorders. Front Endocrinol. 2017;9:178.

Singanwad P, Tatode A, Qutub M, Taksande B, Umekar M, Trivedi R, et al. Neuropeptide Y as a multifaceted modulator of neuroplasticity, Neuroinflammation and HPA axis dysregulation: Perceptions into treatment-resistant depression. Neuropeptides. 2025;12:102538.

Kumari R, Pascalau R, Wang H, Bajpayi S, Yurgel M, Quansah K, et al. Sympathetic NPY controls glucose homeostasis, cold tolerance and cardiovascular functions in mice. Cell Reports. 2024;27;43(2):857.

Hubers SA, Wilson JR, Yu C, Nian H, Grouzmann E, Eugster P, et al. DPP (dipeptidyl peptidase)-4 inhibition potentiates the vasoconstrictor response to NPY (neuropeptide Y) in humans during renin-angiotensin-aldosterone system inhibition. Hypertension. 2018;72(3):712-9.

Tan CM, Green P, Tapoulal N, Lewandowski AJ, Leeson P, Herring N. The role of neuropeptide Y in cardiovascular health and disease. Front Physiol. 2018;9:1281.

Zheng YL, Lin HL, Li YT, Li MM, Du JR, Wang WD, et al. Role of plasma neuropeptide Y in acute myocardial infarction: a case-control study. BMC Cardiovasc Disord. 2024;24(1):692.

Yehuda R, Flory JD, Southwick S, Charney DS: Developing an agenda for translational studies of resilience and vulnerability following trauma exposure. Ann N Y Acad Sci. 2006;1071:379-96.

Morales-Medina JC, Dumont Y, Quirion R: A possible role of neuropeptide Y in depression and stress. Brain Res. 2010;4:194-205.

Enman NM, Sabban EL, McGonigle P, Van Bockstaele EJ. Targeting the neuropeptide Y system in stress-related psychiatric disorders. Neurobiol Stress. 2015;1:33-43.

Dahan M, Zohar J, Todder D, Mathé AA, Cohen H. Exploring the anxiolytic potential of NPY by a dipeptidyl peptidase-IV inhibitor in an animal model of PTSD. Int J Neuropsychopharmacol. 2024;27(12):62.

Reichmann F, Holzer P: Neuropeptide Y: A stressful review. Neuropeptides. 2016;55:99-109.

Sah R, Geracioti TD: Neuropeptide Y and posttraumatic stress disorder. Mol Psych. 2013;18:646-55.

Cattaneo S, Verlengia G, Marino P, Simonato M, Bettegazzi B. NPY and gene therapy for epilepsy: how, when. and Y. Front Mol Neurosci. 2021;22:608001.

Wei X, Cai F, Zhou S, Zhang J, Xu K, Shen G. The neuropeptide Y single-nucleotide polymorphism rs16147: T> C moderates the effect of alcohol dependence on depression in male Chinese Han population. Front Psychiat. 2022;13:1012850.

Katus U, Villa I, Ringmets I, Veidebaum T, Harro J. Neuropeptide Y gene variants in obesity, dietary intake, blood pressure, lipid and glucose metabolism: A longitudinal birth cohort study. Peptides. 2021;139:170524.

Zhang X, Qi Q, Liang J, Hu FB, Sacks FM, Qi L. Neuropeptide Y promoter polymorphism modifies effects of a weight-loss diet on 2-year changes of blood pressure: the preventing overweight using novel dietary strategies trial. Hypertension. 2012;60(5):1169-75.

Chang HA, Fang WH, Chang TC, Huang SY, Chang CC. Association of neuropeptide Y promoter polymorphism (rs16147) with perceived stress and cardiac vagal outflow in humans. Sci Rep. 2016;16:31683.

Morgan III CA, Wang S, Southwick SM, Rasmusson A, Hazlett G, Hauger RL, et al. Plasma neuropeptide-Y concentrations in humans exposed to military survival training. Biol Psych. 2000;47(10):902-9.

Michalkiewicz M, Knestaut KM, Bytchkova EY, Michalkiewicz T. Hypotension and reduced catecholamines in neuropeptide Y transgenic rats. Hypertension. 2003;41(5):1056-62.

Barraco RA, Ergene E, Dunbar JC, Ganduri YL, Anderson GF. Y2 receptors for neuropeptide Y in the nucleus of the solitary tract mediate depressor responses. Peptides. 1991;12(4):691–8.

Cassaglia PA, Shi Z, Li B, Reis WL, Clute-Reinig NM, Stern Je, et al. Neuropeptide Y acts in the paraventricular nucleus to suppress sympathetic nerve activity and its baroreflex regulation. J Physiol. 2014;592(7):1655–75.

Casto R, Phillips MI. Neuropeptide action in nucleus tractus solitarius: angiotensin specificity and hypertensive rats. American J Physiol-Regul, Integ Comp Physiol. 1985;249(3):341-7.

McLean KJ, Jarrott B, Lawrence AJ. Hypotension activates neuropeptide Y-containing neurons in the rat medulla oblongata. Neuroscience. 1999;92(4):1377-87.

Li C, Wu X, Liu S, Zhao Y, Zhu J, Liu K. Roles of neuropeptide Y in neurodegenerative and neuroimmune diseases. Front Neurosci. 2019;13:869.

Yulyaningsih E, Zhang L, Herzog H, Sainsbury A. NPY receptors as potential targets for anti‐obesity drug development. British J Pharmacol. 2011;163(6):1170-202.

Melas PA, Lennartsson A, Vakifahmetoglu-Norberg H, Wei Y, Åberg E, Werme M, et al. Allele-specific programming of Npy and epigenetic effects of physical activity in a genetic model of depression. Transl Psychiat. 2013;3(5):255.

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Published

2025-11-11

How to Cite

Kumari, B. (2025). Genetic modulator of stress resilience and blood pressure regulation: insights from polymorphic variation. International Journal of Research in Medical Sciences. https://doi.org/10.18203/2320-6012.ijrms20253744

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Review Articles