Opioid Receptor-Mediated Modulation of Synaptic Transmission in the Nucleus of the Solitary Tract

  • Li, Cheng-Shu (Department of Anatomy Southern Illinois University School of Medicine)
  • Published : 2009.12.31

Abstract

Keywords

References

  1. Aicher SA, Goldberg A, Sharma S, Pickel VM. mu-opioid receptors are present in vagal afferents and their dendritic targets in the medial nucleus tractus solitarius. J Comp Neurol. 2000; 422: 181-90 https://doi.org/10.1002/(SICI)1096-9861(20000626)422:2<181::AID-CNE3>3.0.CO;2-G
  2. Arbisi PA, Billington CJ, Levine AS. The effect of naltrexone on taste detection and recognition threshold. Appetite. 1999; 32: 241-9 https://doi.org/10.1006/appe.1998.0217
  3. Atkinson RL, Berke LK, Drake CR, Bibbs ML, Williams FL, Kaiser DL. Effects of long-term therapy with naltrexone on body weight in obesity. Clin Pharmacol Ther. 1985; 38: 419-22 https://doi.org/10.1038/clpt.1985.197
  4. Baker RW, Li Y, Lee MG, Sclafani A, Bodnar RJ. Naltrexone does not prevent acquisition or expression of flavor preferences conditioned by fructose in rats. Pharmacol Biochem Behav. 2004; 78: 239-46 https://doi.org/10.1016/j.pbb.2004.03.013
  5. Bertino M, Beauchamp GK, Engelman K. Naltrexone, an opioid blocker, alters taste perception and nutrient intake in humans. Am J Physiol. 1991; 261: R59-63 https://doi.org/10.1152/ajpregu.1991.261.1.R59
  6. Cho YK, Li CS. Gustatory neural circuitry in the hamster brain stem. J Neurophysiol. 2008; 100: 1007-19 https://doi.org/10.1152/jn.01364.2007
  7. Cho YK, Li CS, Smith DV. Gustatory projections from the nucleus of the solitary tract to the parabrachial nuclei in the hamster. Chem Senses. 2002; 27: 81-90 https://doi.org/10.1093/chemse/27.1.81
  8. Cole JL, Leventhal L, Pasternak GW, Bowen WD, Bodnar RJ. Reductions in body weight following chronic central opioid receptor subtype antagonists during development of dietary obesity in rats. Brain Res. 1995; 678: 168-76 https://doi.org/10.1016/0006-8993(95)00181-O
  9. Davis BJ. GABA-like immunoreactivity in the gustatory zone of the nucleus of the solitary tract in the hamster: light and electron microscopic studies. Brain Res Bull. 1993; 30: 69-77 https://doi.org/10.1016/0361-9230(93)90040-I
  10. Davis BJ, Kream RM. Distribution of tachykinin- and opioidexpressing neurons in the hamster solitary nucleus: an immuno- and in situ hybridization histochemical study. Brain Res. 1993; 616: 6-16 https://doi.org/10.1016/0006-8993(93)90185-P
  11. Davis BJ, Smith DV. Substance P modulates taste responses in the nucleus of the solitary tract of the hamster. Neuroreport. 1997; 8: 1723-27 https://doi.org/10.1097/00001756-199705060-00031
  12. Ennis M, Zhou FM, Ciombor KJ, Aroniadou-Anderjaska V, Hayar A, Borrelli E, Zimmer LA, Margolis F, Shipley MT. Dopamine D2 receptor-mediated presynaptic inhibition of olfactory nerve terminals. J Neurophysiol. 2001; 86: 2986-97 https://doi.org/10.1152/jn.2001.86.6.2986
  13. Fantino M, Hosotte J, Apfelbaum M. An opioid antagonist, naltrexone, reduces preference for sucrose in humans. Am J Physiol. 1986; 251: R91-6 https://doi.org/10.1152/ajpregu.1986.251.1.R91
  14. Flood JF, Smith GE, Morley JE. Modulation of memory processing by cholecystokinin: dependence on the vagus nerve. Science. 1987; 236: 832-4 https://doi.org/10.1126/science.3576201
  15. Gutstein HB, Akil H. Opioid analgesics. In: The pharmacological basis of therapeutics, edited by Hardman JG, Limbird LE, and Gilman AG. New York: McGraw-Hill, 2001, p. 259-619
  16. Hadjimarkou MM, Singh A, Kandov Y, Israel Y, Pan YX, Rossi GC, Pasternak GW, Bodnar RJ. Opioid receptor involvement in food deprivation-induced feeding: evaluation of selective antagonist and antisense oligodeoxynucleotide probe effects in mice and rats. J Pharmacol Exp Ther. 2004; 311: 1188-202 https://doi.org/10.1124/jpet.104.071761
  17. Hescheler J, Rosenthal W, Trautwein W, Schultz G. The GTPbinding protein, Go, regulates neuronal calcium channels. Nature. 1987; 325: 445-47 https://doi.org/10.1038/325445a0
  18. Israel Y, Kandov Y, Khaimova E, Kest A, Lewis SR, Pasternak GW, Pan YX, Rossi GC, Bodnar RJ. NPY-induced feeding: pharmacological characterization using selective opioid antagonists and antisense probes in rats. Peptides. 2005; 26: 1167-75 https://doi.org/10.1016/j.peptides.2005.01.017
  19. Jin W, Lee NM, Loh HH, Thayer SA. Dual excitatory and inhibitory effects of opioids on intracellular calcium in neuroblastoma x glioma hybrid NG108-15 cells. Mol Pharmacol. 1992; 42: 1083-9
  20. Jin W, Lee NM, Loh HH, Thayer SA. Opioids mobilize calcium from inositol 1,4,5-trisphosphate-sensitive stores in NG108-15 cells. J Neurosci. 1994; 14: 1920-9
  21. Johnson PS, Wang JB, Wang WF, Uhl GR. Expressed mu opiate receptor couples to adenylate cyclase and phosphatidyl inositol turnover. Neuroreport. 1994; 5: 507-9 https://doi.org/10.1097/00001756-199401120-00035
  22. Kalia M, Fuxe K, Goldstein M. Rat medulla oblongata. II. Dopaminergic, noradrenergic (A1 and A2) and adrenergic neurons, nerve fibers, and presumptive terminal processes. J Comp Neurol. 1985; 233: 308-32 https://doi.org/10.1002/cne.902330303
  23. Kelley AE, Bakshi VP, Haber SN, Steininger TL, Will MJ, Zhang M. Opioid modulation of taste hedonics within the ventral striatum. Physiol Behav. 2002; 76: 365-77 https://doi.org/10.1016/S0031-9384(02)00751-5
  24. King MS, Wang L, Bradley RM. Substance P excites neurons in the gustatory zone of the rat nucleus tractus solitarius. Brain Res. 1993; 619: 120-30 https://doi.org/10.1016/0006-8993(93)91603-P
  25. Kline DD, Takacs KN, Ficker E, Kunze DL. Dopamine modulates synaptic transmission in the nucleus of the solitary tract. J Neurophysiol. 2002; 88: 2736-44 https://doi.org/10.1152/jn.00224.2002
  26. Kotz CM, Glass MJ, Levine AS, Billington CJ. Regional effect of naltrexone in the nucleus of the solitary tract in blockade of NPY-induced feeding. Am J Physiol Regul Integr Comp Physiol. 2000; 278: R499-503 https://doi.org/10.1152/ajpregu.2000.278.2.R499
  27. Kotz CM, Grace MK, Briggs J, Levine AS, Billington CJ. Effects of opioid antagonists naloxone and naltrexone on neuropeptide Y-induced feeding and brown fat thermogenesis in the rat. Neural site of action. J Clin Invest. 1995; 96: 163-70 https://doi.org/10.1172/JCI118017
  28. Levine AS, Grace M, Billington CJ, Zimmerman DM. Central administration of the opioid antagonist, LY255582, decreases short- and long-term food intake in rats. Brain Res. 1991; 566: 193-7 https://doi.org/10.1016/0006-8993(91)91698-Z
  29. Levine AS, Morley JE, Gosnell BA, Billington CJ, Bartness TJ. Opioids and consummatory behavior. Brain Res Bull. 1985; 14: 663-72 https://doi.org/10.1016/0361-9230(85)90116-9
  30. Li CS, Davis BJ, Smith DV. Opioid modulation of taste responses in the nucleus of the solitary tract. Brain Res. 2003; 965: 21-34 https://doi.org/10.1016/S0006-8993(02)03973-2
  31. Li CS, Smith DV. Glutamate receptor antagonists block gustatory afferent input to the nucleus of the solitary tract. J Neurophysiol. 1997; 77: 1514-25 https://doi.org/10.1152/jn.1997.77.3.1514
  32. Liu H, Behbehani MM, Smith DV. The influence of GABA on cells in the gustatory region of the hamster solitary nucleus. Chem Senses. 1993; 18: 285-305 https://doi.org/10.1093/chemse/18.3.285
  33. Lynch WC, Watt J, Krall S, Paden CM. Autoradiographic localization of kappa opiate receptors in CNS taste and feeding areas. Pharmacol Biochem Behav. 1985; 22: 699-705 https://doi.org/10.1016/0091-3057(85)90516-7
  34. Maley BE. Immunohistochemical localization of neuropeptides and neurotransmitters in the nucleus solitarius. Chem Senses. 1996; 21: 367-76 https://doi.org/10.1093/chemse/21.3.367
  35. Maley BE, Panneton WM. Enkephalin-immunoreactive neurons in the nucleus tractus solitarius project to the parabrachial nucleus of the cat. Brain Res. 1988; 442: 340-4 https://doi.org/10.1016/0006-8993(88)91521-1
  36. Mansour A, Fox CA, Burke S, Meng F, Thompson RC, Akil H, Watson SJ. Mu, delta, and kappa opioid receptor mRNA expression in the rat CNS: an in situ hybridization study. J Comp Neurol. 1994; 350: 412-38 https://doi.org/10.1002/cne.903500307
  37. Miles R. Frequency dependence of synaptic transmission in nucleus of the solitary tract in vitro. J Neurophysiol. 1986; 55: 1076-90 https://doi.org/10.1152/jn.1986.55.5.1076
  38. Morley JE, Levine AS, Yim GK, Lowy MT. Opioid modulation of appetite. Neurosci Biobehav Rev. 1983; 7: 281-305 https://doi.org/10.1016/0149-7634(83)90020-9
  39. Murakami S, Okamura H, Yanaihara C, Yanaihara N, Ibata Y. Immunocytochemical distribution of met-enkephalin-Arg6-Gly7-Leu8 in the rat lower brainstem. J Comp Neurol. 1987; 261: 193-208 https://doi.org/10.1002/cne.902610203
  40. Nomura S, Ding YQ, Kaneko T, Li JL, Mizuno N. Localization of mu-opioid receptor-like immunoreactivity in the central components of the vagus nerve: a light and electron microscope study in the rat. Neuroscience. 1996; 73: 277-86 https://doi.org/10.1016/0306-4522(96)00027-9
  41. Park ES, Jo S, Yi SJ, Kim JS, Ee HS, Lee IS, Seo KM, Sung JK, Lee I, Yoon YS. Effect of capsaicin on cholecystokinin and neuropeptide Y expressions in the brain of high-fat diet fed rats. J Vet Med Sci. 2004; 66: 107-14 https://doi.org/10.1292/jvms.66.107
  42. Parker LA, Maier S, Rennie M, Crebolder J. Morphine- and naltrexone-induced modification of palatability: analysis by the taste reactivity test. Behav Neurosci. 1992; 106: 999-1010 https://doi.org/10.1037/0735-7044.106.6.999
  43. Piros ET, Prather PL, Law PY, Evans CJ, Hales TG. Voltagedependent inhibition of Ca2+ channels in GH3 cells by cloned mu- and delta-opioid receptors. Mol Pharmacol. 1996; 50: 947-56
  44. Piros ET, Prather PL, Loh HH, Law PY, Evans CJ, Hales TG. Ca2+ channel and adenylyl cyclase modulation by cloned mu-opioid receptors in GH3 cells. Mol Pharmacol. 1995; 47: 1041-9
  45. Reid LD. Endogenous opioid peptides and regulation of drinking and feeding. Am J Clin Nutr. 1985; 42: 1099-132 https://doi.org/10.1093/ajcn/42.5.1099
  46. Rhee SG. Regulation of phosphoinositide-specific phospholipase C. Annu Rev Biochem. 2001; 70: 281-312 https://doi.org/10.1146/annurev.biochem.70.1.281
  47. Rideout HJ, Parker LA. Morphine enhancement of sucrose palatability: analysis by the taste reactivity test. Pharmacol Biochem Behav. 1996; 53: 731-4 https://doi.org/10.1016/0091-3057(95)02077-2
  48. Sanchez-Blazquez P, Rodriguez-Diaz M, Frejo MT, Garzon J. Stimulation of mu- and delta-opioid receptors enhances phosphoinositide metabolism in mouse spinal cord: evidence for subtypes of delta-receptors. Eur J Neurosci. 1999; 11: 2059-64 https://doi.org/10.1046/j.1460-9568.1999.00624.x
  49. Smart D, Lambert DG. delta-Opioids stimulate inositol 1,4,5-trisphosphate formation, and so mobilize Ca2+ from intracellular stores, in undifferentiated NG108-15 cells. J Neurochem. 1996; 66: 1462-7 https://doi.org/10.1046/j.1471-4159.1996.66041462.x
  50. Smith DV, Li CS. Tonic GABAergic inhibition of tasteresponsive neurons in the nucleus of the solitary tract. Chem Senses. 1998; 23: 159-69 https://doi.org/10.1093/chemse/23.2.159
  51. Spencer RJ, Jin W, Thayer SA, Chakrabarti S, Law PY, Loh HH. Mobilization of Ca2+ from intracellular stores in transfected neuro2a cells by activation of multiple opioid receptor subtypes. Biochem Pharmacol. 1997; 54: 809-18 https://doi.org/10.1016/S0006-2952(97)00243-8
  52. Surprenant A, Shen KZ, North RA, Tatsumi H. Inhibition of calcium currents by noradrenaline, somatostatin and opioids in guinea-pig submucosal neurones. J Physiol. 1990; 431: 585-608 https://doi.org/10.1113/jphysiol.1990.sp018349
  53. Sweazey RD. Distribution of GABA and glycine in the lamb nucleus of the solitary tract. Brain Res. 1996; 737: 275-86 https://doi.org/10.1016/0006-8993(96)00742-1
  54. Tallent M, Dichter MA, Bell GI, Reisine T. The cloned kappa opioid receptor couples to an N-type calcium current in undifferentiated PC-12 cells. Neuroscience. 1994; 63: 1033-40 https://doi.org/10.1016/0306-4522(94)90570-3
  55. Wang L, Bradley RM. In vitro study of afferent synaptic transmission in the rostral gustatory zone of the rat nucleus of the solitary tract. Brain Res. 1995; 702: 88-198 https://doi.org/10.1016/0006-8993(95)01062-6
  56. Wang L, Bradley RM. Influence of GABA on neurons of the gustatory zone of the rat nucleus of the solitary tract. Brain Res. 1993; 616: 144-53 https://doi.org/10.1016/0006-8993(93)90203-Y
  57. Yeomans MR, Gray RW, Mitchell CJ, True S. Independent effects of palatability and within-meal pauses on intake and appetite ratings in human volunteers. Appetite. 1997; 29: 61-76 https://doi.org/10.1006/appe.1997.0092
  58. Yeomans MR, Wright P, Macleod HA, Critchley JA. Effects of nalmefene on feeding in humans. Dissociation of hunger and palatability. Psychopharmacology (Berl). 1990; 100: 426-32 https://doi.org/10.1007/BF02244618
  59. Zucker RS, Regehr WG. Short-term synaptic plasticity. Annu Rev Physiol. 2002; 64: 355-405 https://doi.org/10.1146/annurev.physiol.64.092501.114547