Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

A POMC-originated circuit regulates stress-induced hypophagia, depression, and anhedonia

Abstract

Chronic stress causes dysregulations of mood and energy homeostasis, but the neurocircuitry underlying these alterations remain to be fully elucidated. Here we demonstrate that chronic restraint stress in mice results in hyperactivity of pro-opiomelanocortin neurons in the arcuate nucleus of the hypothalamus (POMCARH neurons) associated with decreased neural activities of dopamine neurons in the ventral tegmental area (DAVTA neurons). We further revealed that POMCARH neurons project to the VTA and provide an inhibitory tone to DAVTA neurons via both direct and indirect neurotransmissions. Finally, we show that photoinhibition of the POMCARH→VTA circuit in mice increases body weight and food intake, and reduces depression-like behaviors and anhedonia in mice exposed to chronic restraint stress. Thus, our results identified a novel neurocircuitry regulating feeding and mood in response to stress.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. McEwen BS, Morrison JH. The brain on stress: vulnerability and plasticity of the prefrontal cortex over the life course. Neuron. 2013;79:16–29.

    CAS  PubMed  PubMed Central  Google Scholar 

  2. Krahn DD, Gosnell BA, Majchrzak MJ. The anorectic effects of CRH and restraint stress decrease with repeated exposures. Biol Psychiatry. 1990;27:1094–102.

    CAS  PubMed  Google Scholar 

  3. Jeong JY, Lee DH, Kang SS. Effects of chronic restraint stress on body weight, food intake, and hypothalamic gene expressions in mice. Endocrinol Metab. 2013;28:288–96.

    Google Scholar 

  4. Chuang JC, Krishnan V, Yu HG, Mason B, Cui H, Wilkinson MB, et al. A beta3-adrenergic-leptin-melanocortin circuit regulates behavioral and metabolic changes induced by chronic stress. Biol Psychiatry. 2010;67:1075–82.

    CAS  PubMed  PubMed Central  Google Scholar 

  5. Holly EN, Miczek KA. Ventral tegmental area dopamine revisited: effects of acute and repeated stress. Psychopharmacology. 2016;233:163–86.

    CAS  PubMed  Google Scholar 

  6. Barker DJ, Root DH, Zhang S, Morales M. Multiplexed neurochemical signaling by neurons of the ventral tegmental area. J Chem Neuroanat. 2016;73:33–42.

    CAS  PubMed  PubMed Central  Google Scholar 

  7. Morales M, Margolis EB. Ventral tegmental area: cellular heterogeneity, connectivity and behaviour. Nat Rev Neurosci. 2017;18:73–85.

    CAS  PubMed  Google Scholar 

  8. Yamaguchi T, Sheen W, Morales M. Glutamatergic neurons are present in the rat ventral tegmental area. Eur J Neurosci. 2007;25:106–18.

    PubMed  PubMed Central  Google Scholar 

  9. Willner P. Dopamine and depression: a review of recent evidence. I. Empirical studies. Brain Res. 1983;287:211–24.

    CAS  PubMed  Google Scholar 

  10. Chiodo LA, Antelman SM. Electroconvulsive shock: progressive dopamine autoreceptor subsensitivity independent of repeated treatment. Science. 1980;210:799–801.

    CAS  PubMed  Google Scholar 

  11. Tye KM, Mirzabekov JJ, Warden MR, Ferenczi EA, Tsai HC, Finkelstein J, et al. Dopamine neurons modulate neural encoding and expression of depression-related behaviour. Nature. 2013;493:537–41.

    CAS  PubMed  Google Scholar 

  12. Friedman AK, Walsh JJ, Juarez B, Ku SM, Chaudhury D, Wang J, et al. Enhancing depression mechanisms in midbrain dopamine neurons achieves homeostatic resilience. Science. 2014;344:313–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Sidor MM, Spencer SM, Dzirasa K, Parekh PK, Tye KM, Warden MR, et al. Daytime spikes in dopaminergic activity drive rapid mood-cycling in mice. Mol Psychiatry. 2015;20:1406–19.

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Liu J, Perez SM, Zhang W, Lodge DJ, Lu XY. Selective deletion of the leptin receptor in dopamine neurons produces anxiogenic-like behavior and increases dopaminergic activity in amygdala. Mol Psychiatry. 2011;16:1024–38.

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Son DH, Doan KV, Yang DJ, Sun JS, Kim SK, Kang N, et al. FoxO1 regulates leptin-induced mood behavior by targeting tyrosine hydroxylase. Metabolism. 2019;91:43–52.

    CAS  PubMed  Google Scholar 

  16. Liu W, Liu J, Xia J, Xue X, Wang H, Qi Z, et al. Leptin receptor knockout-induced depression-like behaviors and attenuated antidepressant effects of exercise are associated with STAT3/SOCS3 signaling. Brain Behav Immun. 2017;61:297–305.

    CAS  PubMed  Google Scholar 

  17. Zhou QY, Palmiter RD. Dopamine-deficient mice are severely hypoactive, adipsic, and aphagic. Cell. 1995;83:1197–209.

    CAS  PubMed  Google Scholar 

  18. Szczypka MS, Rainey MA, Kim DS, Alaynick WA, Marck BT, Matsumoto AM, et al. Feeding behavior in dopamine-deficient mice. Proc Natl Acad Sci USA. 1999;96:12138–43.

    CAS  PubMed  Google Scholar 

  19. Boekhoudt L, Roelofs TJM, de Jong JW, de Leeuw AE, Luijendijk MCM, Wolterink-Donselaar IG, et al. Does activation of midbrain dopamine neurons promote or reduce feeding? Int J Obes. 2017;41:1131–40.

    CAS  Google Scholar 

  20. Elmquist JK, Elias CF, Saper CB. From lesions to leptin: hypothalamic control of food intake and body weight. Neuron. 1999;22:221–32.

    CAS  PubMed  Google Scholar 

  21. Cone RD. Anatomy and regulation of the central melanocortin system. Nat Neurosci. 2005;8:571–8.

    CAS  PubMed  Google Scholar 

  22. Williams DL, Schwartz MW. The melanocortin system as a central integrator of direct and indirect controls of food intake. Am J Physiol Regul Integr Comp Physiol. 2005;289:R2–3.

    CAS  PubMed  Google Scholar 

  23. Cone RD. The central melanocortin system and energy homeostasis. Trends Endocrinol Metab. 1999;10:211–6.

    CAS  PubMed  Google Scholar 

  24. Huszar D, Lynch CA, Fairchild-Huntress V, Dunmore JH, Fang Q, Berkemeier LR, et al. Targeted disruption of the melanocortin-4 receptor results in obesity in mice. Cell. 1997;88:131–41.

    CAS  PubMed  Google Scholar 

  25. Koch M, Varela L, Kim JG, Kim JD, Hernandez-Nuno F, Simonds SE, et al. Hypothalamic POMC neurons promote cannabinoid-induced feeding. Nature. 2015;519:45–50.

    CAS  PubMed  PubMed Central  Google Scholar 

  26. Appleyard SM, Hayward M, Young JI, Butler AA, Cone RD, Rubinstein M, et al. A role for the endogenous opioid beta-endorphin in energy homeostasis. Endocrinology. 2003;144:1753–60.

    CAS  PubMed  Google Scholar 

  27. Yang Y, Atasoy D, Su HH, Sternson SM. Hunger states switch a flip-flop memory circuit via a synaptic AMPK-dependent positive feedback loop. Cell. 2011;146:992–1003.

    CAS  PubMed  PubMed Central  Google Scholar 

  28. Grandison L, Guidotti A. Stimulation of food intake by muscimol and beta endorphin. Neuropharmacology. 1977;16:533–6.

    CAS  PubMed  Google Scholar 

  29. Seo JS, Wei J, Qin L, Kim Y, Yan Z, Greengard P. Cellular and molecular basis for stress-induced depression. Mol Psychiatry. 2017;22:1440–7.

    CAS  PubMed  Google Scholar 

  30. Dietrich MO, Bober J, Ferreira JG, Tellez LA, Mineur YS, Souza DO, et al. AgRP neurons regulate development of dopamine neuronal plasticity and nonfood-associated behaviors. Nat Neurosci. 2012;15:1108–10.

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Leinninger GM, Opland DM, Jo YH, Faouzi M, Christensen L, Cappellucci LA, et al. Leptin action via neurotensin neurons controls orexin, the mesolimbic dopamine system and energy balance. Cell Metab. 2011;14:313–23.

    CAS  PubMed  PubMed Central  Google Scholar 

  32. Wittmann G, Hrabovszky E, Lechan RM. Distinct glutamatergic and GABAergic subsets of hypothalamic pro-opiomelanocortin neurons revealed by in situ hybridization in male rats and mice. J Comp Neurol. 2013;521:3287–302.

    CAS  PubMed  PubMed Central  Google Scholar 

  33. Roseberry AG, Stuhrman K, Dunigan AI. Regulation of the mesocorticolimbic and mesostriatal dopamine systems by alpha-melanocyte stimulating hormone and agouti-related protein. Neurosci Biobehav Rev. 2015;56:15–25.

    CAS  PubMed  Google Scholar 

  34. Anderson EJ, Cakir I, Carrington SJ, Cone RD, Ghamari-Langroudi M, Gillyard T, et al. 60 YEARS OF POMC: regulation of feeding and energy homeostasis by alpha-MSH. J Mol Endocrinol. 2016;56:T157–74.

    CAS  PubMed  PubMed Central  Google Scholar 

  35. Lindblom J, Opmane B, Mutulis F, Mutule I, Petrovska R, Klusa V, et al. The MC4 receptor mediates alpha-MSH induced release of nucleus accumbens dopamine. Neuroreport. 2001;12:2155–8.

    CAS  PubMed  Google Scholar 

  36. Yang SC, Shieh KR. Differential effects of melanin concentrating hormone on the central dopaminergic neurons induced by the cocaine- and amphetamine-regulated transcript peptide. J Neurochem. 2005;92:637–46.

    CAS  PubMed  Google Scholar 

  37. Lippert RN, Ellacott KL, Cone RD. Gender-specific roles for the melanocortin-3 receptor in the regulation of the mesolimbic dopamine system in mice. Endocrinology. 2014;155:1718–27.

    PubMed  PubMed Central  Google Scholar 

  38. Svingos AL, Chavkin C, Colago EE, Pickel VM. Major coexpression of kappa-opioid receptors and the dopamine transporter in nucleus accumbens axonal profiles. Synapse. 2001;42:185–92.

    CAS  PubMed  Google Scholar 

  39. Svingos AL, Clarke CL, Pickel VM. Localization of the delta-opioid receptor and dopamine transporter in the nucleus accumbens shell: implications for opiate and psychostimulant cross-sensitization. Synapse. 1999;34:1–10.

    CAS  PubMed  Google Scholar 

  40. Hipolito L, Sanchez-Catalan MJ, Zanolini I, Polache A, Granero L. Shell/core differences in mu- and delta-opioid receptor modulation of dopamine efflux in nucleus accumbens. Neuropharmacology. 2008;55:183–9.

    CAS  PubMed  Google Scholar 

  41. Chartoff EH, Ebner SR, Sparrow A, Potter D, Baker PM, Ragozzino ME, et al. Relative timing between kappa opioid receptor activation and cocaine determines the impact on reward and dopamine release. Neuropsychopharmacology. 2016;41:989–1002.

    CAS  PubMed  Google Scholar 

  42. Johnson SW, North RA. Opioids excite dopamine neurons by hyperpolarization of local interneurons. J Neurosci. 1992;12:483–8.

    CAS  PubMed  PubMed Central  Google Scholar 

  43. Kudo T, Konno K, Uchigashima M, Yanagawa Y, Sora I, Minami M, et al. GABAergic neurons in the ventral tegmental area receive dual GABA/enkephalin-mediated inhibitory inputs from the bed nucleus of the stria terminalis. Eur J Neurosci. 2014;39:1796–809.

    PubMed  Google Scholar 

  44. Korotkova TM, Brown RE, Sergeeva OA, Ponomarenko AA, Haas HL. Effects of arousal- and feeding-related neuropeptides on dopaminergic and GABAergic neurons in the ventral tegmental area of the rat. Eur J Neurosci. 2006;23:2677–85.

    CAS  PubMed  Google Scholar 

  45. van Zessen R, Phillips JL, Budygin EA, Stuber GD. Activation of VTA GABA neurons disrupts reward consumption. Neuron. 2012;73:1184–94.

    PubMed  PubMed Central  Google Scholar 

  46. Kaufling J, Veinante P, Pawlowski SA, Freund-Mercier MJ, Barrot M. gamma-Aminobutyric acid cells with cocaine-induced DeltaFosB in the ventral tegmental area innervate mesolimbic neurons. Biol Psychiatry. 2010;67:88–92.

    CAS  PubMed  Google Scholar 

  47. Jarvie BC, Hentges ST. Expression of GABAergic and glutamatergic phenotypic markers in hypothalamic proopiomelanocortin neurons. J Comp Neurol. 2012;520:3863–76.

    CAS  PubMed  PubMed Central  Google Scholar 

  48. Wang D, He X, Zhao Z, Feng Q, Lin R, Sun Y, et al. Whole-brain mapping of the direct inputs and axonal projections of POMC and AgRP neurons. Front Neuroanat. 2015;9:40.

    PubMed  PubMed Central  Google Scholar 

  49. Lutz PE, Kieffer BL. Opioid receptors: distinct roles in mood disorders. Trends Neurosci. 2013;36:195–206.

    CAS  PubMed  Google Scholar 

  50. Komatsu H, Ohara A, Sasaki K, Abe H, Hattori H, Hall FS, et al. Decreased response to social defeat stress in mu-opioid-receptor knockout mice. Pharm Biochem Behav. 2011;99:676–82.

    CAS  Google Scholar 

  51. Nikulina EM, Arrillaga-Romany I, Miczek KA, Hammer RP Jr. Long-lasting alteration in mesocorticolimbic structures after repeated social defeat stress in rats: time course of mu-opioid receptor mRNA and FosB/DeltaFosB immunoreactivity. Eur J Neurosci. 2008;27:2272–84.

    PubMed  PubMed Central  Google Scholar 

  52. Nikulina EM, Hammer RP Jr, Miczek KA, Kream RM. Social defeat stress increases expression of mu-opioid receptor mRNA in rat ventral tegmental area. Neuroreport. 1999;10:3015–9.

    CAS  PubMed  Google Scholar 

  53. Johnston CE, Herschel DJ, Lasek AW, Hammer RP Jr, Nikulina EM. Knockdown of ventral tegmental area mu-opioid receptors in rats prevents effects of social defeat stress: implications for amphetamine cross-sensitization, social avoidance, weight regulation and expression of brain-derived neurotrophic factor. Neuropharmacology. 2015;89:325–34.

    CAS  PubMed  PubMed Central  Google Scholar 

  54. Shanmugarajah L, Dunigan AI, Frantz KJ, Roseberry AG. Altered sucrose self-administration following injection of melanocortin receptor agonists and antagonists into the ventral tegmental area. Psychopharmacology. 2017;234:1683–92.

    CAS  PubMed  Google Scholar 

  55. Yen HH, Roseberry AG. Decreased consumption of rewarding sucrose solutions after injection of melanocortins into the ventral tegmental area of rats. Psychopharmacology. 2015;232:285–94.

    CAS  PubMed  Google Scholar 

  56. Roseberry AG. Altered feeding and body weight following melanocortin administration to the ventral tegmental area in adult rats. Psychopharmacology. 2013;226:25–34.

    CAS  PubMed  Google Scholar 

  57. Zhan C, Zhou J, Feng Q, Zhang JE, Lin S, Bao J, et al. Acute and long-term suppression of feeding behavior by POMC neurons in the brainstem and hypothalamus, respectively. J Neurosci. 2013;33:3624–32.

    CAS  PubMed  PubMed Central  Google Scholar 

  58. Balthasar N, Dalgaard LT, Lee CE, Yu J, Funahashi H, Williams T, et al. Divergence of melanocortin pathways in the control of food intake and energy expenditure. Cell. 2005;123:493–505.

    CAS  PubMed  Google Scholar 

  59. Grupe DW, Nitschke JB. Uncertainty and anticipation in anxiety: an integrated neurobiological and psychological perspective. Nat Rev Neurosci. 2013;14:488–501.

    CAS  PubMed  PubMed Central  Google Scholar 

  60. Dietrich MO, Zimmer MR, Bober J, Horvath TL. Hypothalamic Agrp neurons drive stereotypic behaviors beyond feeding. Cell. 2015;160:1222–32.

    CAS  PubMed  PubMed Central  Google Scholar 

  61. Burnett CJ, Li C, Webber E, Tsaousidou E, Xue SY, Bruning JC, et al. Hunger-driven motivational state competition. Neuron. 2016;92:187–201.

    CAS  PubMed  PubMed Central  Google Scholar 

  62. Padilla SL, Qiu J, Soden ME, Sanz E, Nestor CC, Barker FD, et al. Agouti-related peptide neural circuits mediate adaptive behaviors in the starved state. Nat Neurosci. 2016;19:734–41.

    CAS  PubMed  PubMed Central  Google Scholar 

  63. Alhadeff AL, Su Z, Hernandez E, Klima ML, Phillips SZ, Holland RA, et al. A neural circuit for the suppression of pain by a competing need state. Cell. 2018;173:140–52.e115.

    CAS  PubMed  PubMed Central  Google Scholar 

  64. Val-Laillet D, Aarts E, Weber B, Ferrari M, Quaresima V, Stoeckel LE, et al. Neuroimaging and neuromodulation approaches to study eating behavior and prevent and treat eating disorders and obesity. Neuroimage Clin. 2015;8:1–31.

    CAS  PubMed  PubMed Central  Google Scholar 

  65. Kumar P, Goer F, Murray L, Dillon DG, Beltzer ML, Cohen AL, et al. Impaired reward prediction error encoding and striatal-midbrain connectivity in depression. Neuropsychopharmacology. 2018;43:1581–8.

    PubMed  PubMed Central  Google Scholar 

  66. Wagner G, de la Cruz F, Kohler S, Bar KJ. Treatment associated changes of functional connectivity of midbrain/brainstem nuclei in major depressive disorder. Sci Rep. 2017;7:8675.

    PubMed  PubMed Central  Google Scholar 

  67. Swann G, Byck GR, Dick DM, Aliev F, Latendresse SJ, Riley B, et al. Effect of OPRM1 and stressful life events on symptoms of major depression in African American adolescents. J Affect Disord. 2014;162:12–19.

    CAS  PubMed  PubMed Central  Google Scholar 

  68. Madisen L, Zwingman TA, Sunkin SM, Oh SW, Zariwala HA, Gu H, et al. A robust and high-throughput Cre reporting and characterization system for the whole mouse brain. Nat Neurosci. 2010;13:133–40.

    CAS  PubMed  Google Scholar 

  69. Berglund ED, Liu C, Sohn JW, Liu T, Kim MH, Lee CE, et al. Serotonin 2C receptors in pro-opiomelanocortin neurons regulate energy and glucose homeostasis. J Clin Invest. 2013;123:5061–70.

    CAS  PubMed  PubMed Central  Google Scholar 

  70. Tong Q, Ye CP, Jones JE, Elmquist JK, Lowell BB. Synaptic release of GABA by AgRP neurons is required for normal regulation of energy balance. Nat Neurosci. 2008;11:998–100.

    CAS  PubMed  PubMed Central  Google Scholar 

  71. Vong L, Ye C, Yang Z, Choi B, Chua S Jr, Lowell BB. Leptin action on GABAergic neurons prevents obesity and reduces inhibitory tone to POMC neurons. Neuron. 2011;71:142–54.

    CAS  PubMed  PubMed Central  Google Scholar 

  72. Balthasar N, Coppari R, McMinn J, Liu SM, Lee CE, Tang V, et al. Leptin receptor signaling in POMC neurons is required for normal body weight homeostasis. Neuron. 2004;42:983–91.

    CAS  PubMed  Google Scholar 

  73. Galassetti P, Tate D, Neill RA, Morrey S, Wasserman DH, Davis SN. Effect of sex on counterregulatory responses to exercise after antecedent hypoglycemia in type 1 diabetes. Am J Physiol Endocrinol Metab. 2004;287:E16–24.

    CAS  PubMed  Google Scholar 

  74. Atasoy D, Aponte Y, Su HH, Sternson SM. A FLEX switch targets Channelrhodopsin-2 to multiple cell types for imaging and long-range circuit mapping. J Neurosci. 2008;28:7025–30.

    CAS  PubMed  PubMed Central  Google Scholar 

  75. Petreanu L, Huber D, Sobczyk A, Svoboda K. Channelrhodopsin-2-assisted circuit mapping of long-range callosal projections. Nat Neurosci. 2007;10:663–8.

    CAS  PubMed  Google Scholar 

  76. Fan W, Boston BA, Kesterson RA, Hruby VJ, Cone RD. Role of melanocortinergic neurons in feeding and the agouti obesity syndrome. Nature. 1997;385:165–8.

    CAS  PubMed  Google Scholar 

  77. Fenalti G, Giguere PM, Katritch V, Huang XP, Thompson AA, Cherezov V, et al. Molecular control of delta-opioid receptor signalling. Nature. 2014;506:191–6.

    CAS  PubMed  PubMed Central  Google Scholar 

  78. Wu H, Wacker D, Mileni M, Katritch V, Han GW, Vardy E, et al. Structure of the human kappa-opioid receptor in complex with JDTic. Nature. 2012;485:327–32.

    CAS  PubMed  PubMed Central  Google Scholar 

  79. Spetea M, Schullner F, Moisa RC, Berzetei-Gurske IP, Schraml B, Dorfler C, et al. Synthesis and biological evaluation of 14-alkoxymorphinans. 21. Novel 4-alkoxy and 14-phenylpropoxy derivatives of the mu opioid receptor antagonist cyprodime. J Med Chem. 2004;47:3242–7.

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported by grants from the NIH (K99DK107008 to PX; R01DK111436, R01ES027544, R21CA215591 to ZS), USDA/CRIS (6250-51000-059-04S to YX), American Diabetes Association (1-17-PDF-138 to YH), American Heart Association awards (17GRNT32960003 to YX, 16GRNT30970064 to ZS, and 16POST27260254 to CW), National Natural Science Foundation of China (81400886 to NQ), Hubei Province health and family planning scientific research project (WJ2015Q033 to NQ) and Population and Family Planning Commission of Wuhan (WX14B34 to NQ). We also appreciated support by award and fellowships from Wuhan Young & Middle-Aged Talents, Health and Family Planning Commission of Wuhan Municipality and China Scholarship Council (File No. 201608420019 to NQ).

Author information

Authors and Affiliations

Authors

Contributions

NQ, YH, and CW were involved in experimental design and most of procedures, data acquisition and analyses, and writing the manuscript. PX, YY, XC, HL, KY, ZP, and IH assisted in production of study mice, surgical procedures, and blinded evaluation of mouse behaviors. ZS, MF, YL, and QL were involved in study design and writing the manuscript. YX is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Corresponding author

Correspondence to Yong Xu.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Qu, N., He, Y., Wang, C. et al. A POMC-originated circuit regulates stress-induced hypophagia, depression, and anhedonia. Mol Psychiatry 25, 1006–1021 (2020). https://doi.org/10.1038/s41380-019-0506-1

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41380-019-0506-1

This article is cited by

Search

Quick links