Characterization and distribution of an arginine vasotocin receptor in mouse

Journal of Veterinary Medical Science

Volumn 68, Issue 7, 2006, Pages 655-661

  Usui, Masaru ^a   Aoshima, Hitoshi ^a   Yamamoto, Yoshimi ^a   Luziga, Claudius ^a   Mamba, Koichi ^a  

^a YAMAGUCHI UNIVERSITY   (Japan)

Author keywords

Arg8 vasotocin; G protein coupled receptor; in situ hybridization; Voltage clamp

Indexed keywords

VASOPRESSIN RECEPTOR; VASOTOCIN RECEPTOR;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; CHEMISTRY; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; MOLECULAR GENETICS; MOUSE; NUCLEOTIDE SEQUENCE; OOCYTE; XENOPUS LAEVIS;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; GENE EXPRESSION REGULATION; MICE; MOLECULAR SEQUENCE DATA; OOCYTES; RECEPTORS, VASOPRESSIN; XENOPUS LAEVIS;

PLATICHTHYS FLESUS; TELEOSTEI; XENOPUS LAEVIS;

EID: 33746877572     PISSN: 09167250     EISSN: 13477439     Source Type: Journal    
DOI: 10.1292/jvms.68.655     Document Type: Article

References (43)

1. Antle, M.C. and Silver, R. 2005. Orchestrating time: arrangements of the brain circadian clock. Trends Neurosci. 28: 145-151.
2. Badiu, C., Coculescu, M. and Moller, M. 1999. Arginine vasotocin mRNA revealed by in situ hybridization in bovine pineal gland cells. Cell Tissue Res. 295: 225-229.
3. Barbacka-Surowiak, G., Surowiak, J. and Stoklosowa, S. 2003. The involvement of suprachiasmatic nuclei in the regulation of estrous cycles in rodents. Reprod. Biol. 3: 99-129.
4. Barberis, C. and Tribollet, E. 1996. Vasopressin and oxytocin receptors in the central nervous system. Crit. Rev. Neurobiol. 10: 119-154.
5. Berridge, M.J. 1993. Inositol trisphosphate and calcium signaling. Nature (Lond.) 361: 315-325.
6. Birnbaumer, M. 2000. Vasopressin receptors. Trends Endocrinol. Metab. 11: 406-410.
7. Blumenau, C., Berger, E., Fauteck, J.D., Madeja, M., Wittkowski, W., Speckmann, E.J. and Musshoff, U. 2001. Expression and functional characterization of the mt1 melatonin receptor from rat brain in Xenopus oocytes: evidence for coupling to the phosphoinositol pathway. J. Pineal Res. 30: 139-146.
8. Cone, R.D., Cowley, M.A., Butler, A.A., Fan, W., Marks, D.L. and Low, M.J. 2001. The arcuate nucleus as a conduit for diverse signals relevant to energy homeostasis. Int. J. Obes. Relat. Metab. Disord. (Suppl.) 5: S63-67.
9. de la Pena, P., del Camino, D., Pardo, L.A., Dominguez, P. and Barros, F. 1995. Gs couples thyrotropin-releasing hormone receptors expressed in Xenopus oocytes to phospholipase C. J. Biol. Chem. 270: 3554-3559.
10. Dixon, R.A., Sigal, I.S., Candelore, M.R., Register, R.B., Scattergood, W., Rands, E. and Strader, C.D. 1987. Structural features required for ligand binding to the beta-adrenergic receptor. EMBO J. 6: 3269-3275.
11. Ferguson, S.S. 1998. Using green fluorescent protein to understand the mechanisms of G-protein-coupled receptor regulation. Braz. J. Med. Biol. Res. 31: 1471-1477.
12. Figueroa, J., Morley, S.D., Heierhorst, J., Krentler, C., Lederis, K. and Richter, D. 1989. Two isotocin genes are present in the white sucker Catostomus commersoni both lacking introns in their protein coding regions. EMBO J. 8: 2873-2877.
13. Gilchriest, B.J., Tipping, D.R., Levy, A. and Baker, B.I. 1998. Diurnal changes in the expression of genes encoding for arginine vasotocin and pituitary pro-opiomelanocortin in the rainbow trout (Oncorhynchus mykiss): correlation with changes in plasma hormones. J. Neuroendocrinol. 10: 937-943.
14. Goldstein, R. 1989. Habenular nuclei specifically bind synthetic arginine vasotocin. Endocrinology 27: 237-239.
15. Goldstein, R. 1992. Arginine-vasotocin (AVT) - a pineal hormone in mammals. Rom. J. Endocrinol. 30: 21-44.
16. 8] vasotocin receptor. Proc. Natl. Acad. Sci. U.S.A. 93: 6907-6912.
17. Hilakivi, I., Taira, T. and Hilakivi, L.A. 1988. Effect of peripheral administration of arginine vasotocin on neonatal sleep in rats. Peptides 9: 487-491.
18. 8] vasotocin excites neurones in the dorsal vagal complex in vitro: evidence for an action through novel class(es) of CNS receptors. J. Neuroendocrinol. 6: 415-422.
19. Kasahara, J. and Sugiyama, H. 1994. Inositol phospholipid metabolism in Xenopus oocytes mediated by endogenous G(o) and Gi proteins. FEBS Lett. 355: 41-44.
20. Kawasawa, Y., McKenzie, L.M., Hill, D.P., Bono, H., Yanagisawa, M.; RIKEN GER Group; GSR Members. 2003. G protein-coupled receptor genes in the FANTOM2 database. Genome Res. 13: 1466-1477.
21. Kimura, T., Tanizawa, O., Mori, K., Brownstein, M.J. and Okayama, H. 1992. Structure and expression of a human oxytocin receptor. Nature (Lond.) 356: 526-529.
22. Kubo, T., Fukuda, K., Mikami, A., Maeda, A., Takahashi, H., Mishina, M., Haga, T., Haga, K., Ichiyama, A., Kangawa, K. et al. 1986. Cloning, sequencing and expression of complementary DNA encoding the muscarinic acetylcholine receptor. Nature (Lond.) 323: 411-416.
23. Leedom, L., Lewis, C., Garcia-Segura, L.M. and Naftolin, F. 1994. Regulation of arcuate nucleus synaptology by estrogen. Ann. New York Acad. Sci. 743: 61-71.
24. Liu, B. and Burbach, J.P. 1987. Characterization of vasopressin and oxytocin immunoreactivity in the sheep and rat pineal gland: absence of vasotocin and detection of a vasopressin-like peptide. Peptides 8: 7-11.
25. Masu, M., Tanabe, Y., Tsuchida, K., Shigemoto, R. and Nakanishi, S. 1991. Sequence and expression of a metabotropic glutamate receptor. Nature (Lond.) 349: 760-765.
26. 8] vasotocin on the firing rate of suprachiasmatic neurons in vitro. Neuroscience 62: 783-792.
27. Miyamae, T., Fukushima, N., Misu, Y. and Ueda, H. 1993. Delta opioid receptor mediates phospholipase C activation via Gi in Xenopus oocytes. FEBS Lett. 333: 311-314.
28. Moons, L., Cambre, M., Batten, T.F. and Vandesande, F. 1989. Autoradiographic localization of binding sites for vasotocin in the brain and pituitary of the sea bass (Dicentrarchus labrax). Neurosci. Lett. 100: 11-16.
29. Moriarty, T.M., Padrell, E., Carty, D.J., Omri, G., Landau, E.M. and Iyengar, R. 1990. Go protein as signal transducer in the pertussis toxin-sensitive phosphatidylinositol pathway. Nature (Lond.) 343: 79-82.
30. 2+ signaling evoked by stimulation of the vasopressin V1a receptor. J. Biol. Chem. 267: 23282-23289.
31. Pavel, S. 1978. Arginine vasotocin as a pineal hormone. J. Neural. Transm. (Suppl.) 13: 135-155.
32. Pavel, S. and Eisner, C. 1984. A GABAergic habenulo-raphe pathway mediates both serotoninergic and hypnogenic effects of vasotocin in cats. Brain Res. Bull. 13: 623-627.
33. Prechel, M.M., Audhya, T.K. and Simmons, W.H. 1989. Influence of age on August levels of pineal immunoreactive arginine vasotocin in rats. J. Pineal Res. 6: 1-7.
34. Rose, J.D. and Moore, F.L. 2002. Behavioral neuroendocrinology of vasotocin and vasopressin and the sensorimotor processing hypothesis. Front. Neuroendocrinol. 23: 317-341.
35. Sambrook, J. and Russel, D.W. 2001. A Laboratory Manual, 3rd ed., Cold Spring Harbor Laboratory Press, New York.
36. Sandyk, R. 1991. Relevance of the habenular complex to neuropsychiatry: a review and hypothesis. Int. J. Neurosci. 61: 189-219
37. Sartin, J.L., Brout, B.C. and Orts, R.J. 1979. Neurotransmitter regulation of arginine vasotocin release from rat pineal glands in vitro. Acta. Endocrinol. (Copenh) 91: 571-576.
38. Thompson, R.R. and Moore, F.L. 2000. Vasotocin stimulates appetitive responses to the visual and pheromonal stimuli used by male roughskin newts during courtship. Horm. Behav. 38: 75-85.
39. 5Tyr(Me)VP in the rat brain, pituitary and kidney. Neurosci. Lett. 80: 121-126.
40. Warne, J. 2002. The role of arginine vasotocin in teleost fish osmoregulation. Symp. Soc. Exp. Biol. 54: 83-95.
41. Warne, J.M. 2001. Cloning and characterization of an arginine vasotocin receptor from the euryhaline flounder Platichthys flesus. Gen. Comp. Endocrinol. 122: 312-319.
42. Xu, Y.L., Reinscheid, R.K., Huitron-Resendiz, S., Clark, S.D., Wang, Z., Lin, S.H., Brucher, F.A., Zeng, J., Ly, N.K., Henriksen, S.J., de Lecea, L. and Civelli, O. 2004. Neuropeptide S: a neuropeptide promoting arousal and anxiolytic-like effects. Neuron 43: 487-497.
43. Zingg, H.H. and Laporte, S.A. 2003. The oxytocin receptor. Trends Endocrinol. Metab. 14: 222-227.