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2014 Fiscal Year Final Research Report

Physiological function of the rat SDN-POA analyzed by sst-siRNA recombinant adenovirus vector

Research Project

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Project/Area Number 23590285
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Environmental physiology (including Physical medicine and Nutritional physiology)
Research InstitutionNippon Medical School

Principal Investigator

ORIKASA Chitose  日本医科大学, 付置研究所, 講師 (20270671)

Co-Investigator(Renkei-kenkyūsha) MIYAKA Koichi  日本医科大学, 医学部, 准教授 (90267211)
Project Period (FY) 2011-04-28 – 2015-03-31
KeywordsSDN-POA / calbindin / ソマトスタチン / 性的二系核 / siRNA / sexual behavior / male rat
Outline of Final Research Achievements

We have shown earlier that during development, somatostatin (sst) gene is transiently transcribed in neurons in the sexually dimorphic nucleus of the rat preoptic area (SDN-POA) characterized by calbindin immunoreactivity. We hypothesized that mechanisms other than apoptosis are involved in the establishment of the SDN-POA. BrdU immunoreactivity showed up in calbindin-labeled neurons in the SDN-POA of PD15 cohorts treated on 14, 16 or 18 embryonic days (ED). The number of BrdU-positive neurons was largest in animals given BrdU on 18 ED. Daily injections of BrdU during postnatal day 1-10 labeled a few calbindin-immunoreactive cells in the SDN-POA of PD15 brain of male and female rats. Next step, we analyzed the physiological function of the male rat SDN-POA by the treatments of sst-siRNA recombinant adenovirus vector and esi sst-siRNA followed by preference and sexual behavior test. Sst neurons expressed in the SDN-POA are unlikely involved in sexual behavior of male rat.

Free Research Field

神経内分泌学

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Published: 2016-06-03  

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