Age- and sex-specific changes in naloxone-induced luteinizing hormone secretion and Fos expression in gonadotropin-releasing hormone neurons of gonadectomized rats

被引:3
作者
Funabashi, Toahiya [1 ,2 ]
Furuta, Miyako [1 ,2 ]
Fukushima, Atsushi [2 ]
Kimura, Fukuko [2 ,3 ]
机构
[1] St Marianna Univ, Dept Physiol, Sch Med, Miyamae Ku, Kawasaki, Kanagawa 2168511, Japan
[2] Yokohama City Univ, Grad Sch Med, Dept Physiol, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[3] Int Univ Hlth & Welf, Minato Ku, Tokyo 1070062, Japan
关键词
Opioid; Pulse; Luteinizing hormone; Gonadotropin-releasing hormone; Immediate early genes; PULSE-GENERATOR ACTIVITY; ELECTRICAL-ACTIVITY; RHESUS-MONKEY; LHRH NEURONS; FEMALE RATS; FEEDBACK; ANDROGEN; MEN; INCREASES; FREQUENCY;
D O I
10.1016/j.neulet.2010.01.032
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the present study, we examined sex-specific changes in luteinizing hormone (LH) secretion and Fos expression in gonadotropin-releasing hormone (GnRH) neurons in response to naloxone in Young (3 months old) and old (24 months old), gonadectomized male and female rats. We revealed by immunocytochemistry that, regardless of age and sex, naloxone significantly increased the number of GnRH neurons expressing Fos, which was associated with increased LH secretion. Additionally, although the magnitude of the increase in Fos-expressing GnRH neurons did not change in old males compared to young males, it was attenuated by almost half in old females compared to young females. LH levels decreased 60% in old males compared to young males and 15% in old females compared to young females. These results suggest LH secretion is impaired with age, but the ability of GnRH neurons to be stimulated by naloxone is preserved. However, the opioid-control ling mechanism is more fragile in females than males during aging. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:157 / 161
页数:5
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