| Journal of Veterinary Medical Science | |
| Characterization and Distribution of an Arginine Vasotocin Receptor in Mouse | |
| Hitoshi AOSHIMA2  Claudius LUZIGA1  Yoshimi YAMAMOTO1  Masaru USUI1  Koichi MAMBA1  | |
| [1] Department of Veterinary Sciences, Faculty of Agriculture, Yamaguchi University;Department of Physics, Biology and Informatics, Faculty of Science, Yamaguchi University | |
| 关键词: [Arg8] vasotocin; G protein-coupled receptor; in situ hybridization; voltage clamp; | |
| DOI : 10.1292/jvms.68.655 | |
| 学科分类:兽医学 | |
| 来源: Japanese Society of Veterinary Science | |
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【 摘 要 】
References(43)Cited-By(2)A cDNA, which has a high homology with teleost Platichthys flesus [Arg8] vasotocin (AVT) receptor (GenBank: AK033957), was found in mouse genome database. Analyses of the deduced amino acid sequence revealed that a cDNA has several features of AVT receptor. We tentatively named it as a mouse vasotocin receptor (MVTR). A two-electrodes voltage clamp technique was applied to characterize the MVTR expressed in Xenopus laevis oocytes. AVT induced Ca2+-dependent Cl- currents in Xenopus oocytes injected with MVTR cRNA. On the other hand, [Arg8] vasopressin, oxytocin and isotocin did not induce such currents. RT-PCR showed that MVTR mRNA was specifically expressed in the brain. In situ hybridization analysis demonstrated significant expression of MVTR mRNA in suprachiasmatic nucleus, arcuate nucleus and medial habenular nucleus of mouse brain. These results suggest that MVTR may mediate a variety of physiological functions in mouse.
【 授权许可】
Unknown
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201911300865696ZK.pdf | 564KB |
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