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.

  • Review Article
  • Published:

Lateral hypothalamic circuits for feeding and reward

Abstract

In experiments conducted over 60 years ago, the lateral hypothalamic area (LHA) was identified as a critical neuroanatomical substrate for motivated behavior. Electrical stimulation of the LHA induces voracious feeding even in well-fed animals. In the absence of food, animals will work tirelessly, often lever-pressing thousands of times per hour, for electrical stimulation at the same site that provokes feeding, drinking and other species-typical motivated behaviors. Here we review the classic findings from electrical stimulation studies and integrate them with more recent work that has used contemporary circuit-based approaches to study the LHA. We identify specific anatomically and molecularly defined LHA elements that integrate diverse information arising from cortical, extended amygdala and basal forebrain networks to ultimately generate a highly specified and invigorated behavioral state conveyed via LHA projections to downstream reward and feeding-specific circuits.

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

Figure 1: Electrical stimulation of the LHA produces reinforcement.
Figure 2: The LHA contains a mixture of inhibitory and excitatory neurons.
Figure 3: Vgat-targeted neurons are distinct from MCH- and Orx-producing LHA neurons.
Figure 4: Proposed neurocircuit-wiring diagram based on optogenetic studies.

Similar content being viewed by others

References

  1. Broberger, C., De Lecea, L., Sutcliffe, J.G. & Hökfelt, T. Hypocretin/orexin- and melanin-concentrating hormone-expressing cells form distinct populations in the rodent lateral hypothalamus: relationship to the neuropeptide Y and agouti gene-related protein systems. J. Comp. Neurol. 402, 460–474 (1998).

    CAS  PubMed  Google Scholar 

  2. Lee, H. et al. Scalable control of mounting and attack by Esr1+ neurons in the ventromedial hypothalamus. Nature 509, 627–632 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Lein, E.S. et al. Genome-wide atlas of gene expression in the adult mouse brain. Nature 445, 168–176 (2007).

    CAS  PubMed  Google Scholar 

  4. Puelles, L. & Rubenstein, J.L.R. Forebrain gene expression domains and the evolving prosomeric model. Trends Neurosci. 26, 469–476 (2003).

    CAS  PubMed  Google Scholar 

  5. Saper, C.B., Chou, T.C. & Elmquist, J.K. The need to feed: homeostatic and hedonic control of eating. Neuron 36, 199–211 (2002).

    CAS  PubMed  Google Scholar 

  6. Hess, W.R. The Functional Organization of the Diencephalon (Grune & Stratton, New York, 1957).

  7. Martini, L. & Ganong, W.F. Neuroendocrinology (Elsevier, 2013).

  8. Swaab, D.F. et al. The Human Hypothalamus in Health and Disease (Elsevier, 1992).

  9. Bernardis, L.L. & Bellinger, L.L. The lateral hypothalamic area revisited: neuroanatomy, body weight regulation, neuroendocrinology and metabolism. Neurosci. Biobehav. Rev. 17, 141–193 (1993).

    CAS  PubMed  Google Scholar 

  10. Millhouse, O.E. A Golgi study of the desending medial forebrain bundle. Brain Res. 15, 341–363 (1969).

    CAS  PubMed  Google Scholar 

  11. Palkovits, M. & Van Cuc, H. Quantitative light and electron microscopic studies on the lateral hypothalamus in rat. Cell and synaptic densities. Brain Res. Bull. 5, 643–647 (1980).

    CAS  PubMed  Google Scholar 

  12. Berthoud, H.-R. & Münzberg, H. The lateral hypothalamus as integrator of metabolic and environmental needs: from electrical self-stimulation to opto-genetics. Physiol. Behav. 104, 29–39 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Nieuwenhuys, R., Geeraedts, L.M. & Veening, J.G. The medial forebrain bundle of the rat. I. General introduction. J. Comp. Neurol. 206, 49–81 (1982).

    CAS  PubMed  Google Scholar 

  14. Anand, B.K. & Brobeck, J.R. Localization of a 'feeding center' in the hypothalamus of the rat. Proc. Soc. Exp. Biol. Med. 77, 323–324 (1951).

    CAS  PubMed  Google Scholar 

  15. Montemurro, D.G. & Stevenson, J.A. Adipsia produced by hypothalamic lesions in the rat. Can. J. Biochem. Physiol. 35, 31–37 (1957).

    CAS  PubMed  Google Scholar 

  16. Hetherington, A.W. & Ranson, S.W. Hypothalamic lesions and adiposity in the rat. Anat. Rec. 78, 149–172 (1940).

    Google Scholar 

  17. Ungerstedt, U. Adipsia and aphagia after 6-hydroxydopamine induced degeneration of the nigro-striatal dopamine system. Acta Physiol. Scand. Suppl. 367, 95–122 (1971).

    CAS  PubMed  Google Scholar 

  18. Kapatos, G. & Gold, R.M. Evidence for ascending noradrenergic mediation of hypothalamic hyperphagia. Pharmacol. Biochem. Behav. 1, 81–87 (1973).

    CAS  PubMed  Google Scholar 

  19. Grossman, S.P., Dacey, D., Halaris, A.E., Collier, T. & Routtenberg, A. Aphagia and adipsia after preferential destruction of nerve cell bodies in hypothalamus. Science 202, 537–539 (1978).

    CAS  PubMed  Google Scholar 

  20. Grossman, S.P. & Grossman, L. Iontophoretic injections of kainic acid into the rat lateral hypothalamus: effects on ingestive behavior. Physiol. Behav. 29, 553–559 (1982).

    CAS  PubMed  Google Scholar 

  21. Stricker, E.M., Swerdloff, A.F. & Zigmond, M.J. Intrahypothalamic injections of kainic acid produce feeding and drinking deficits in rats. Brain Res. 158, 470–473 (1978).

    CAS  PubMed  Google Scholar 

  22. Delgado, J.M. & Anand, B.K. Increase of food intake induced by electrical stimulation of the lateral hypothalamus. Am. J. Physiol. 172, 162–168 (1953).

    CAS  PubMed  Google Scholar 

  23. Olds, J. & Milner, P. Positive reinforcement produced by electrical stimulation of septal area and other regions of rat brain. J. Comp. Physiol. Psychol. 47, 419–427 (1954).

    CAS  PubMed  Google Scholar 

  24. Hoebel, B.G. & Teitelbaum, P. Hypothalamic control of feeding and self-stimulation. Science 135, 375–377 (1962).

    CAS  PubMed  Google Scholar 

  25. Margules, D.L. & Olds, J. Identical “feeding” and “rewarding” systems in the lateral hypothalamus of rats. Science 135, 374–375 (1962).

    CAS  PubMed  Google Scholar 

  26. Stanley, B.G., Ha, L.H., Spears, L.C. & Dee, M.G. II. Lateral hypothalamic injections of glutamate, kainic acid, D,L-alpha-amino-3-hydroxy-5-methyl-isoxazole propionic acid or N-methyl-D-aspartic acid rapidly elicit intense transient eating in rats. Brain Res. 613, 88–95 (1993).

    CAS  PubMed  Google Scholar 

  27. Kelly, J., Rothstein, J. & Grossman, S.P. GABA and hypothalamic feeding systems. I. Topographic analysis of the effects of microinjections of muscimol. Physiol. Behav. 23, 1123–1134 (1979).

    CAS  PubMed  Google Scholar 

  28. Bower, G.H. & Miller, N.E. Rewarding and punishing effects from stimulating the same place in the rat's brain. J. Comp. Physiol. Psychol. 51, 669–674 (1958).

    CAS  PubMed  Google Scholar 

  29. Mendelson, J. & Freed, W.J. Do rats terminate hypothalamic stimulation only in order to turn it on again? Behav. Biol. 8, 619–628 (1973).

    CAS  PubMed  Google Scholar 

  30. Caggiula, A.R. & Hoebel, B.G. “Copulation-reward site” in the posterior hypothalamus. Science 153, 1284–1285 (1966).

    CAS  PubMed  Google Scholar 

  31. Mogenson, G.J. & Stevenson, J.A. Drinking induced by electrical stimulation of the lateral hypothalamus. Exp. Neurol. 17, 119–127 (1967).

    CAS  PubMed  Google Scholar 

  32. Roberts, W.W. & Carey, R.J. Rewarding effect of performance of gnawing aroused by hypothalamic stimulation in the rat. J. Comp. Physiol. Psychol. 59, 317–324 (1965).

    CAS  PubMed  Google Scholar 

  33. Glickman, S.E. & Schiff, B.B. A biological theory of reinforcement. Psychol. Rev. 74, 81–109 (1967).

    CAS  PubMed  Google Scholar 

  34. Hutchinson, R.R. & Renfrew, J.W. Stalking attack and eating behaviors elicited from the same sites in the hypothalamus. J. Comp. Physiol. Psychol. 61, 360–367 (1966).

    CAS  PubMed  Google Scholar 

  35. Coons, E.E., Levak, M. & Miller, N.E. Lateral hypothalamus: learning of food-seeking response motivated by electrical stimulation. Science 150, 1320–1321 (1965).

    CAS  PubMed  Google Scholar 

  36. Wise, R.A. Individual differences in effects of hypothalamic stimulation: the role of stimulation locus. Physiol. Behav. 6, 569–572 (1971).

    CAS  PubMed  Google Scholar 

  37. Valenstein, E.S., Cox, V.C. & Kakolewski, J.W. Modification of motivated behavior elicited by electrical stimulation of the hypothalamus. Science 159, 1119–1121 (1968).

    CAS  PubMed  Google Scholar 

  38. Wise, R.A. Hypothalamic motivational systems: fixed or plastic neural circuits? Science 162, 377–379 (1968).

    CAS  PubMed  Google Scholar 

  39. Mendleson, J. The role of hunger in the T-maze learning for food by rats. J. Comp. Physiol. Psychol. 62, 341–349 (1966).

    Google Scholar 

  40. Mendelson, J. & Chorover, S.L. Lateral hypothalamic stimulation in satiated rats: T-maze learning for food. Science 149, 559–561 (1965).

    CAS  PubMed  Google Scholar 

  41. Andersson, B. & Wyrwicka, W. The elicitation of a drinking motor conditioned reaction by electrical stimulation of the hypothalamic drinking area in the goat. Acta Physiol. Scand. 41, 194–198 (1957).

    CAS  PubMed  Google Scholar 

  42. Tenen, S.S. & Miller, N.E. Strength of electrical stimulation of lateral hypothalamus, food deprivation, and tolerance for quinine in food. J. Comp. Physiol. Psychol. 58, 55–62 (1964).

    CAS  PubMed  Google Scholar 

  43. Wise, R.A. & Albin, J. Stimulation-induced eating disrupted by a conditioned taste aversion. Behav. Biol. 9, 289–297 (1973).

    CAS  PubMed  Google Scholar 

  44. Flynn, J.P. Neural aspects of attack behavior in cats. Ann. NY Acad. Sci. 159, 1008–1012 (1969).

    CAS  PubMed  Google Scholar 

  45. MacDonnell, M. & Flynn, J.P. Sensory control of hypothalamic attack. Anim. Behav. 14, 399–405 (1966).

    CAS  PubMed  Google Scholar 

  46. MacDonnell, M.F. & Flynn, J.P. Control of sensory fields by stimulation of hypothalamus. Science 152, 1406–1408 (1966).

    CAS  PubMed  Google Scholar 

  47. Fulton, S., Woodside, B. & Shizgal, P. Modulation of brain reward circuitry by leptin. Science 287, 125–128 (2000).

    CAS  PubMed  Google Scholar 

  48. Fulton, S., Woodside, B. & Shizgal, P. Potentiation of brain stimulation reward by weight loss: evidence for functional heterogeneity in brain reward circuitry. Behav. Brain Res. 174, 56–63 (2006).

    PubMed  Google Scholar 

  49. Mogenson, G.J., Gentil, C.G. & Stevenson, J.A. Feeding and drinking elicited by low and high frequencies of hypothalamic stimulation. Brain Res. 33, 127–137 (1971).

    CAS  PubMed  Google Scholar 

  50. Morgane, P.J. Evidence of a 'hunger motivational' system in the lateral hypothalamus of the rat. Nature 191, 672–674 (1961).

    CAS  PubMed  Google Scholar 

  51. Ranck, J.B. Jr. Which elements are excited in electrical stimulation of mammalian central nervous system: a review. Brain Res. 98, 417–440 (1975).

    PubMed  Google Scholar 

  52. Greer, M.A. Suggestive evidence of a primary drinking center in hypothalamus of the rat. Proc. Soc. Exp. Biol. Med. S 89, 59–62 (1955).

    CAS  Google Scholar 

  53. Olds, J. Pleasure centers in the brain. Sci. Am. 195, 105–116 (1956).

    Google Scholar 

  54. Wise, R.A. Lateral hypothalamic electrical stimulation: does it make animals 'hungry'? Brain Res. 67, 187–209 (1974).

    CAS  PubMed  Google Scholar 

  55. Wise, R.A. Dual roles of dopamine in food and drug seeking: the drive-reward paradox. Biol. Psychiatry 73, 819–826 (2013).

    CAS  PubMed  Google Scholar 

  56. Phillips, A.G. & Nikaido, R.S. Disruption of brain stimulation-induced feeding by dopamine receptor blockade. Nature 258, 750–751 (1975).

    CAS  PubMed  Google Scholar 

  57. Fouriezos, G., Hansson, P. & Wise, R.A. Neuroleptic-induced attenuation of brain stimulation reward in rats. J. Comp. Physiol. Psychol. 92, 661–671 (1978).

    CAS  PubMed  Google Scholar 

  58. Fouriezos, G. & Wise, R.A. Pimozide-induced extinction of intracranial self-stimulation: response patterns rule out motor or performance deficits. Brain Res. 103, 377–380 (1976).

    CAS  PubMed  Google Scholar 

  59. Franklin, K.B. Catecholamines and self-stimulation: reward and performances effects dissociated. Pharmacol. Biochem. Behav. 9, 813–820 (1978).

    CAS  PubMed  Google Scholar 

  60. Franklin, K.B. & McCoy, S.N. Pimozide-induced extinction in rats: stimulus control of responding rules out motor deficit. Pharmacol. Biochem. Behav. 11, 71–75 (1979).

    CAS  PubMed  Google Scholar 

  61. Gallistel, C.R., Boytim, M., Gomita, Y. & Klebanoff, L. Does pimozide block the reinforcing effect of brain stimulation? Pharmacol. Biochem. Behav. 17, 769–781 (1982).

    CAS  PubMed  Google Scholar 

  62. Wise, R.A. Catecholamine theories of reward: a critical review. Brain Res. 152, 215–247 (1978).

    CAS  PubMed  Google Scholar 

  63. Gallistel, C.R., Shizgal, P. & Yeomans, J.S. A portrait of the substrate for self-stimulation. Psychol. Rev. 88, 228–273 (1981).

    CAS  PubMed  Google Scholar 

  64. Yeomans, J.S. The absolute refractory periods of self-stimulation neurons. Physiol. Behav. 22, 911–919 (1979).

    CAS  PubMed  Google Scholar 

  65. Gratton, A. & Wise, R.A. Hypothalamic reward mechanism: two first-stage fiber populations with a cholinergic component. Science 227, 545–548 (1985).

    CAS  PubMed  Google Scholar 

  66. Shizgal, P., Bielajew, C., Corbett, D., Skelton, R. & Yeomans, J. Behavioral methods for inferring anatomical linkage between rewarding brain stimulation sites. J. Comp. Physiol. Psychol. 94, 227–237 (1980).

    CAS  PubMed  Google Scholar 

  67. Bielajew, C. & Shizgal, P. Evidence implicating descending fibers in self-stimulation of the medial forebrain bundle. J. Neurosci. 6, 919–929 (1986).

    CAS  PubMed  PubMed Central  Google Scholar 

  68. Bielajew, C., Bushnik, T., Konkle, A.T. & Schindler, D. The substrate for brain-stimulation reward in the lateral preoptic area. II. Connections to the ventral tegmental area. Brain Res. 881, 112–120 (2000).

    CAS  PubMed  Google Scholar 

  69. Wise, R.A. & Bozarth, M.A. Brain substrates for reinforcement and drug self-administration. Prog. Neuropsychopharmacol. 5, 467–474 (1981).

    CAS  PubMed  Google Scholar 

  70. Yeomans, J.S. The cells and axons mediating medial forebrain bundle reward. in The Neural Basis of Feeding and Reward (eds. Hoebel, B.G. & Novin, D.) 405–417 (Haer Institute, 1982).

  71. Wise, R.A., Spindler, J., deWit, H. & Gerberg, G.J. Neuroleptic-induced “anhedonia” in rats: pimozide blocks reward quality of food. Science 201, 262–264 (1978).

    CAS  PubMed  Google Scholar 

  72. De Wit, H. & Wise, R.A. Blockade of cocaine reinforcement in rats with the dopamine receptor blocker pimozide, but not with the noradrenergic blockers phentolamine or phenoxybenzamine. Can. J. Psychol. 31, 195–203 (1977).

    CAS  PubMed  Google Scholar 

  73. Yokel, R.A. & Wise, R.A. Increased lever pressing for amphetamine after pimozide in rats: implications for a dopamine theory of reward. Science 187, 547–549 (1975).

    CAS  PubMed  Google Scholar 

  74. Gratton, A. & Wise, R.A. Comparisons of refractory periods for medial forebrain bundle fibers subserving stimulation-induced feeding and brain stimulation reward: a psychophysical study. Brain Res. 438, 256–263 (1988).

    CAS  PubMed  Google Scholar 

  75. Gratton, A. & Wise, R.A. Comparisons of connectivity and conduction velocities for medial forebrain bundle fibers subserving stimulation-induced feeding and brain stimulation reward. Brain Res. 438, 264–270 (1988).

    CAS  PubMed  Google Scholar 

  76. Allen, G.V. & Cechetto, D.F. Neurotensin in the lateral hypothalamic area: origin and function. Neuroscience 69, 533–544 (1995).

    CAS  PubMed  Google Scholar 

  77. Burdakov, D. & Alexopoulos, H. Metabolic state signalling through central hypocretin/orexin neurons. J. Cell. Mol. Med. 9, 795–803 (2005).

    PubMed  PubMed Central  Google Scholar 

  78. Collin, M. et al. Plasma membrane and vesicular glutamate transporter mRNAs/proteins in hypothalamic neurons that regulate body weight. Eur. J. Neurosci. 18, 1265–1278 (2003).

    PubMed  Google Scholar 

  79. Goforth, P.B., Leinninger, G.M., Patterson, C.M., Satin, L.S. & Myers, M.G. Jr. Leptin acts via lateral hypothalamic area neurotensin neurons to inhibit orexin neurons by multiple GABA-independent mechanisms. J. Neurosci. 34, 11405–11415 (2014).

    PubMed  PubMed Central  Google Scholar 

  80. Griffond, B. & Risold, P.Y. MCH and feeding behavior-interaction with peptidic network. Peptides 30, 2045–2051 (2009).

    CAS  PubMed  Google Scholar 

  81. Knight, Z.A. et al. Molecular profiling of activated neurons by phosphorylated ribosome capture. Cell 151, 1126–1137 (2012).

    CAS  PubMed  Google Scholar 

  82. Laque, A. et al. Leptin receptor neurons in the mouse hypothalamus are colocalized with the neuropeptide galanin and mediate anorexigenic leptin action. Am. J. Physiol. Endocrinol. Metab. 304, E999–E1011 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  83. Leinninger, G.M. et al. Leptin acts via leptin receptor-expressing lateral hypothalamic neurons to modulate the mesolimbic dopamine system and suppress feeding. Cell Metab. 10, 89–98 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  84. Rosin, D.L., Weston, M.C., Sevigny, C.P., Stornetta, R.L. & Guyenet, P.G. Hypothalamic orexin (hypocretin) neurons express vesicular glutamate transporters VGLUT1 or VGLUT2. J. Comp. Neurol. 465, 593–603 (2003).

    CAS  PubMed  Google Scholar 

  85. Ziegler, D.R., Cullinan, W.E. & Herman, J.P. Distribution of vesicular glutamate transporter mRNA in rat hypothalamus. J. Comp. Neurol. 448, 217–229 (2002).

    CAS  PubMed  Google Scholar 

  86. Acuna-Goycolea, C., Tamamaki, N., Yanagawa, Y., Obata, K. & van den Pol, A.N. Mechanisms of neuropeptide Y, peptide YY, and pancreatic polypeptide inhibition of identified green fluorescent protein-expressing GABA neurons in the hypothalamic neuroendocrine arcuate nucleus. J. Neurosci. 25, 7406–7419 (2005).

    CAS  PubMed  PubMed Central  Google Scholar 

  87. Karnani, M.M., Szabó, G., Erdélyi, F. & Burdakov, D. Lateral hypothalamic GAD65 neurons are spontaneously firing and distinct from orexin- and melanin-concentrating hormone neurons. J. Physiol. (Lond.) 591, 933–953 (2013).

    CAS  Google Scholar 

  88. Luiten, P.G.M., ter Horst, G.J. & Steffens, A.B. The hypothalamus, intrinsic connections and outflow pathways to the endocrine system in relation to the control of feeding and metabolism. Prog. Neurobiol. 28, 1–54 (1987).

    CAS  PubMed  Google Scholar 

  89. de Lecea, L. et al. The hypocretins: hypothalamus-specific peptides with neuroexcitatory activity. Proc. Natl. Acad. Sci. USA 95, 322–327 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  90. Harrison, T.A., Chen, C.T., Dun, N.J. & Chang, J.K. Hypothalamic orexin A-immunoreactive neurons project to the rat dorsal medulla. Neurosci. Lett. 273, 17–20 (1999).

    CAS  PubMed  Google Scholar 

  91. Sakurai, T. Orexins and orexin receptors: implication in feeding behavior. Regul. Pept. 85, 25–30 (1999).

    CAS  PubMed  Google Scholar 

  92. Haynes, A.C. et al. Anorectic, thermogenic and anti-obesity activity of a selective orexin-1 receptor antagonist in ob/ob mice. Regul. Pept. 104, 153–159 (2002).

    CAS  PubMed  Google Scholar 

  93. Harris, G.C., Wimmer, M. & Aston-Jones, G. A role for lateral hypothalamic orexin neurons in reward seeking. Nature 437, 556–559 (2005).

    CAS  PubMed  Google Scholar 

  94. Adamantidis, A.R., Zhang, F., Aravanis, A.M., Deisseroth, K. & de Lecea, L. Neural substrates of awakening probed with optogenetic control of hypocretin neurons. Nature 450, 420–424 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  95. Hara, J. et al. Genetic ablation of orexin neurons in mice results in narcolepsy, hypophagia, and obesity. Neuron 30, 345–354 (2001).

    CAS  PubMed  Google Scholar 

  96. Sakurai, T. The role of orexin in motivated behaviours. Nat. Rev. Neurosci. 15, 719–731 (2014).

    CAS  PubMed  Google Scholar 

  97. Bittencourt, J.C. et al. The melanin-concentrating hormone system of the rat brain: an immuno- and hybridization histochemical characterization. J. Comp. Neurol. 319, 218–245 (1992).

    CAS  PubMed  Google Scholar 

  98. Elias, C.F. et al. Chemically defined projections linking the mediobasal hypothalamus and the lateral hypothalamic area. J. Comp. Neurol. 402, 442–459 (1998).

    CAS  PubMed  Google Scholar 

  99. Harthoorn, L.F., Sañé, A., Nethe, M. & Van Heerikhuize, J.J. Multi-transcriptional profiling of melanin-concentrating hormone and orexin-containing neurons. Cell. Mol. Neurobiol. 25, 1209–1223 (2005).

    PubMed  Google Scholar 

  100. Jego, S. et al. Optogenetic identification of a rapid eye movement sleep modulatory circuit in the hypothalamus. Nat. Neurosci. 16, 1637–1643 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  101. Qu, D. et al. A role for melanin-concentrating hormone in the central regulation of feeding behaviour. Nature 380, 243–247 (1996).

    CAS  PubMed  Google Scholar 

  102. Ludwig, D.S. et al. Melanin-concentrating hormone overexpression in transgenic mice leads to obesity and insulin resistance. J. Clin. Invest. 107, 379–386 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  103. Alon, T. & Friedman, J.M. Late-onset leanness in mice with targeted ablation of melanin concentrating hormone neurons. J. Neurosci. 26, 389–397 (2006).

    CAS  PubMed  PubMed Central  Google Scholar 

  104. Shimada, M., Tritos, N.A., Lowell, B.B., Flier, J.S. & Maratos-Flier, E. Mice lacking melanin-concentrating hormone are hypophagic and lean. Nature 396, 670–674 (1998).

    CAS  PubMed  Google Scholar 

  105. Brown, J.A., Woodworth, H.L. & Leinninger, G.M. To ingest or rest? Specialized roles of lateral hypothalamic area neurons in coordinating energy balance. Front. Syst. Neurosci. 9, 9 (2015).

    PubMed  PubMed Central  Google Scholar 

  106. Kahn, D., Abrams, G.M., Zimmerman, E.A., Carraway, R. & Leeman, S.E. Neurotensin neurons in the rat hypothalamus: an immunocytochemical study. Endocrinology 107, 47–54 (1980).

    CAS  PubMed  Google Scholar 

  107. Cooke, J.H. et al. Peripheral and central administration of xenin and neurotensin suppress food intake in rodents. Obesity (Silver Spring) 17, 1135–1143 (2009).

    CAS  Google Scholar 

  108. Kim, E.R., Leckstrom, A. & Mizuno, T.M. Impaired anorectic effect of leptin in neurotensin receptor 1-deficient mice. Behav. Brain Res. 194, 66–71 (2008).

    CAS  PubMed  Google Scholar 

  109. Leinninger, G.M. et al. Leptin action via neurotensin neurons controls orexin, the mesolimbic dopamine system and energy balance. Cell Metab. 14, 313–323 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  110. Vong, L. et al. Leptin action on GABAergic neurons prevents obesity and reduces inhibitory tone to POMC neurons. Neuron 71, 142–154 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  111. Jennings, J.H. et al. Visualizing hypothalamic network dynamics for appetitive and consummatory behaviors. Cell 160, 516–527 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  112. Jennings, J.H., Rizzi, G., Stamatakis, A.M., Ung, R.L. & Stuber, G.D. The inhibitory circuit architecture of the lateral hypothalamus orchestrates feeding. Science 341, 1517–1521 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  113. Stamatakis, A.M. et al. Lateral hypothalamic glutamatergic neurons regulate feeding and reward via projections to the lateral habenula. J. Neurosci. (in the press).

  114. Kita, H. & Oomura, Y. Reciprocal connections between the lateral hypothalamus and the frontal complex in the rat: electrophysiological and anatomical observations. Brain Res. 213, 1–16 (1981).

    CAS  PubMed  Google Scholar 

  115. Nauta, W.J.H. Hippocampal projections and related neural pathways to the midbrain in the cat. Brain 81, 319–340 (1958).

    CAS  PubMed  Google Scholar 

  116. Anthony, T.E. et al. Control of stress-induced persistent anxiety by an extra-amygdala septohypothalamic circuit. Cell 156, 522–536 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  117. Heimer, L., Zahm, D.S., Churchill, L., Kalivas, P.W. & Wohltmann, C. Specificity in the projection patterns of accumbal core and shell in the rat. Neuroscience 41, 89–125 (1991).

    CAS  PubMed  Google Scholar 

  118. Zahm, D.S. & Brog, J.S. On the significance of subterritories in the “accumbens” part of the rat ventral striatum. Neuroscience 50, 751–767 (1992).

    CAS  PubMed  Google Scholar 

  119. Root, D.H., Melendez, R.I., Zaborszky, L. & Napier, T.C. The ventral pallidum: subregion-specific functional anatomy and roles in motivated behaviors. Prog. Neurobiol. 130, 29–70 (2015).

    PubMed  PubMed Central  Google Scholar 

  120. Grove, E.A. Efferent connections of the substantia innominata in the rat. J. Comp. Neurol. 277, 347–364 (1988).

    CAS  PubMed  Google Scholar 

  121. Yoshida, K., McCormack, S., España, R.A., Crocker, A. & Scammell, T.E. Afferents to the orexin neurons of the rat brain. J. Comp. Neurol. 494, 845–861 (2006).

    PubMed  PubMed Central  Google Scholar 

  122. Jones, B.E. & Moore, R.Y. Ascending projections of the locus coeruleus in the rat. II. Autoradiographic study. Brain Res. 127, 25–53 (1977).

    CAS  PubMed  Google Scholar 

  123. Moore, R.Y., Halaris, A.E. & Jones, B.E. Serotonin neurons of the midbrain raphe: ascending projections. J. Comp. Neurol. 180, 417–438 (1978).

    CAS  PubMed  Google Scholar 

  124. Betley, J.N., Cao, Z.F.H., Ritola, K.D. & Sternson, S.M. Parallel, redundant circuit organization for homeostatic control of feeding behavior. Cell 155, 1337–1350 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  125. Wu, Z. et al. GABAergic projections from lateral hypothalamus to paraventricular hypothalamic nucleus promote feeding. J. Neurosci. 35, 3312–3318 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  126. Canteras, N.S., Simerly, R.B. & Swanson, L.W. Organization of projections from the ventromedial nucleus of the hypothalamus: a Phaseolus vulgaris-leucoagglutinin study in the rat. J. Comp. Neurol. 348, 41–79 (1994).

    CAS  PubMed  Google Scholar 

  127. O'Connor, E.C. et al. Accumbal D1R neurons projecting to lateral hypothalamus authorize feeding. Neuron 88, 553–564 (2015).

    CAS  PubMed  Google Scholar 

  128. Maldonado-Irizarry, C.S., Swanson, C.J. & Kelley, A.E. Glutamate receptors in the nucleus accumbens shell control feeding behavior via the lateral hypothalamus. J. Neurosci. 15, 6779–6788 (1995).

    CAS  PubMed  PubMed Central  Google Scholar 

  129. Stratford, T.R. & Kelley, A.E. GABA in the nucleus accumbens shell participates in the central regulation of feeding behavior. J. Neurosci. 17, 4434–4440 (1997).

    CAS  PubMed  PubMed Central  Google Scholar 

  130. Stratford, T.R. & Kelley, A.E. Evidence of a functional relationship between the nucleus accumbens shell and lateral hypothalamus subserving the control of feeding behavior. J. Neurosci. 19, 11040–11048 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  131. Behbehani, M.M. Functional characteristics of the midbrain periaqueductal gray. Prog. Neurobiol. 46, 575–605 (1995).

    CAS  PubMed  Google Scholar 

  132. Berk, M.L. & Finkelstein, J.A. Efferent connections of the lateral hypothalamic area of the rat: an autoradiographic investigation. Brain Res. Bull. 8, 511–526 (1982).

    CAS  PubMed  Google Scholar 

  133. Nieh, E.H. et al. Decoding neural circuits that control compulsive sucrose seeking. Cell 160, 528–541 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  134. Jennings, J.H. et al. Distinct extended amygdala circuits for divergent motivational states. Nature 496, 224–228 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  135. Kempadoo, K.A. et al. Hypothalamic neurotensin projections promote reward by enhancing glutamate transmission in the VTA. J. Neurosci. 33, 7618–7626 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  136. van Zessen, R., Phillips, J.L., Budygin, E.A. & Stuber, G.D. Activation of VTA GABA neurons disrupts reward consumption. Neuron 73, 1184–1194 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  137. Tan, K.R. et al. GABA neurons of the VTA drive conditioned place aversion. Neuron 73, 1173–1183 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  138. Poller, W.C., Madai, V.I., Bernard, R., Laube, G. & Veh, R.W. A glutamatergic projection from the lateral hypothalamus targets VTA-projecting neurons in the lateral habenula of the rat. Brain Res. 1507, 45–60 (2013).

    CAS  PubMed  Google Scholar 

  139. Lammel, S. et al. Input-specific control of reward and aversion in the ventral tegmental area. Nature 491, 212–217 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  140. Shabel, S.J., Proulx, C.D., Trias, A., Murphy, R.T. & Malinow, R. Input to the lateral habenula from the basal ganglia is excitatory, aversive, and suppressed by serotonin. Neuron 74, 475–481 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  141. Stratford, T.R. & Wirtshafter, D. Injections of muscimol into the paraventricular thalamic nucleus, but not mediodorsal thalamic nuclei, induce feeding in rats. Brain Res. 1490, 128–133 (2013).

    CAS  PubMed  Google Scholar 

  142. Carter, M.E., Soden, M.E., Zweifel, L.S. & Palmiter, R.D. Genetic identification of a neural circuit that suppresses appetite. Nature 503, 111–114 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  143. Carter, M.E., Han, S. & Palmiter, R.D. Parabrachial calcitonin gene-related peptide neurons mediate conditioned taste aversion. J. Neurosci. 35, 4582–4586 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  144. Horvath, T.L., Diano, S. & van den Pol, A.N. Synaptic interaction between hypocretin (orexin) and neuropeptide Y cells in the rodent and primate hypothalamus: a novel circuit implicated in metabolic and endocrine regulations. J. Neurosci. 19, 1072–1087 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  145. Fukuda, M., Ono, T., Nishino, H. & Nakamura, K. Neuronal responses in monkey lateral hypothalamus during operant feeding behavior. Brain Res. Bull. 17, 879–883 (1986).

    CAS  PubMed  Google Scholar 

  146. Ono, T., Nakamura, K., Nishijo, H. & Fukuda, M. Hypothalamic neuron involvement in integration of reward, aversion, and cue signals. J. Neurophysiol. 56, 63–79 (1986).

    CAS  PubMed  Google Scholar 

  147. Ono, T., Nakamura, K., Fukuda, M. & Kobayashi, T. Catecholamine and acetylcholine sensitivity of rat lateral hypothalamic neurons related to learning. J. Neurophysiol. 67, 265–279 (1992).

    CAS  PubMed  Google Scholar 

  148. Schwartzbaum, J.S. Electrophysiology of taste, feeding and reward in lateral hypothalamus of rabbit. Physiol. Behav. 44, 507–526 (1988).

    CAS  PubMed  Google Scholar 

  149. Macosko, E.Z. et al. Highly parallel genome-wide expression profiling of individual cells using nanoliter droplets. Cell 161, 1202–1214 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  150. Olds, J. Self-stimulation of the brain; its use to study local effects of hunger, sex, and drugs. Science 127, 315–324 (1958).

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We thank J. Jennings for input on the manuscript and members of the Stuber laboratory for helpful discussion. This work was supported by the Klarman Family Foundation, the Brain and Behavior Research Foundation, the Foundation for Prader-Willi Research, the Foundation of Hope, the National Institute on Drug Abuse (DA032750 and DA038168), and the Department of Psychiatry at UNC Chapel Hill (G.D.S.). R.A.W. was supported by the Intramural Research Program at the National Institute on Drug Abuse.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Garret D Stuber.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Stuber, G., Wise, R. Lateral hypothalamic circuits for feeding and reward. Nat Neurosci 19, 198–205 (2016). https://doi.org/10.1038/nn.4220

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nn.4220

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing