Kisspeptin in the Hypothalamus of 2 Rat Models of Polycystic Ovary Syndrome.

Abstract:

:Hyperandrogenism, disturbance of the hypothalamus-pituitary-ovary axis followed by elevated serum luteinizing hormone (LH) levels, and insulin resistance are involved in the complicated pathophysiology of polycystic ovary syndrome (PCOS). Kisspeptin is coexpressed with neurokinin B (NKB) in the arcuate nucleus (ARC), the center of the gonadotropin-releasing hormone pulse generator that is responsible for pulsatile LH secretion. We compared 2 androgenized rat models of PCOS to evaluate the estrous cycle, hormonal profiles, and expression of kisspeptin and NKB in the ARC. Rats in our postnatal dihydrotestosterone (DHT)-treatment model exhibited weight gain and persistent diestrus with normal LH levels. In contrast, irregular cycles, with elevated LH serum levels and normal body weight, were found in the prenatally DHT-treated rats. We also found increased signals of kisspeptin and NKB in the ARC of the prenatally DHT-treated rats, and not in the postnatally DHT-treated rats. Our results suggest that prenatal exposure to androgens may result in higher kisspeptin and NKB levels in the ARC, which could be associated with 1 phenotype of PCOS that is characterized by normal body weight and higher LH secretion, whereas in postnatally DHT-treated rats, characteristics such as weight gain and normal LH levels are seen in the obese PCOS phenotype.

journal_name

Endocrinology

journal_title

Endocrinology

authors

Osuka S,Iwase A,Nakahara T,Kondo M,Saito A,Bayasula,Nakamura T,Takikawa S,Goto M,Kotani T,Kikkawa F

doi

10.1210/en.2016-1333

subject

Has Abstract

pub_date

2017-02-01 00:00:00

pages

367-377

issue

2

eissn

0013-7227

issn

1945-7170

journal_volume

158

pub_type

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