Papers

Basic information

Name OZAWA Hitoshi

Title

Neurokinin B- and kisspeptin-positive fibers as well as tuberoinfundibular dopaminergic neurons directly innervate periventricular hypophyseal dopaminergic neurons in rats and mice

Author

Nobuhiko Sawai,Norio Iijima,Hitoshi Ozawa,Toshiyuki Matsuzaki

Sole or Joint Author

 

Journal

NEUROSCIENCE RESEARCH

Publisher

ELSEVIER IRELAND LTD

All Volumes

 

All Pages

 

Volume

84

Number

 

Starting Page

10

Ending Page

18

Publication Date

2014-07

Referee Paper

Refereed

Invited Paper

Not invited

Language

English

MISC Class

 

Publishing Type

Research paper (scientific journal)

ISSN

 

ID:DOI

10.1016/j.neures.2014.05.002

ID:NAID

 

ID:PMID

 

URL

Description

Neurons co-expressing kisspeptin, neurokinin B (NKB), and dynorphin in the hypothalamic arcuate nucleus, named KNDy neurons, are directly affected by sex hormones, and are well known for regulating the secretion of gonadotropin-releasing hormone. However, recent studies have shown that KNDy neurons also project and terminate to tuberoinfundibular dopaminergic (TIDA) neurons, suggesting a role in prolactin secretion. Moreover, there is a possibility that other neurosecretory dopaminergic neurons regulating prolactin secretion, such as periventricular hypophyseal dopaminergic (PHDA) neurons, may also be innervated by KNDy neurons. In the present study, by means of double immunohistochemistry and retrograde neural tracer, we examined whether KNDy neurons project directly to PHDA neurons that project to blood vessels, as well as to TIDA neurons. The results revealed that KNDy neurons are widely projecting to neurosecretory dopaminergic neurons of the PHDA and TIDA neurons in rats and mice. Secondary, presence of a major receptor for NKB, neurokinin-3 receptor (NK3R), in PHDA and TIDA neurons was examined and it appeared that most TIDA and PHDA neurons possess NK3R. These findings indicate that, in rodents, KNDy neurons widely project to neurosecretory dopaminergic neurons distributed in the hypothalamus, and may affect them via the NKB-NK3R signaling pathway. (C) 2014 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.

ID:JGlobalID

 

arXiv ID

 

Put Code of ORCID

 

DBLP ID

 

WekoID of OpenDepo