Photoperiod regulates leptin sensitivity in field voles, Microtus agrestis

被引:41
作者
Król, E
Duncan, JS
Redman, P
Morgan, PJ
Mercer, JG
Speakman, JR
机构
[1] Univ Aberdeen, Sch Biol Sci, ACERO, Aberdeen AB24 2TZ, Scotland
[2] ACERO, Div Obes & Metab Hlth, Rowett Res Inst, Aberdeen AB21 9SB, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
leptin resistance; chronic cold exposure; circulating leptin levels; uncoupling protein 1 (UCP1); seasonal mammals;
D O I
10.1007/s00360-005-0037-8
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We have previously shown that cold-acclimated (8 degrees C) male field voles (Microtus agrestis) transferred from short (SD, 8:16 h L:D) to long photoperiod (LD, 16:8 h L:D) exhibit increases in body mass, adiposity and food intake. To assess whether these increases were associated with decreased leptin sensitivity, we infused LD and SD voles with physiological doses of murine leptin (or saline) delivered peripherally for 7 days via mini-osmotic pumps. Measurements were made of body mass (weight-reducing effect of leptin), food intake (anorectic effect of leptin) and gene expression of uncoupling protein 1 (UCP1) in brown adipose tissue (BAT) (thermogenic effect of leptin). The SD animals were sensitive to the weight-reducing effects of leptin (mean body mass decrease of 1.2 g over 7 days) and appetite-reducing effect of leptin (mean food intake decrease of 2.5 g over 7 days), whereas LD voles were resistant to the hormone treatment. The switch from a leptin-sensitive to leptin-resistant state appears to act as a desensitisation mechanism that allows voles transferred from SD to LD to ignore elevated leptin levels generated by increased body fat and accumulate adipose tissue without stimulating compensatory changes opposing the weight gain. Neither SD nor LD voles responded to infusion of leptin by changes in BAT UCP1 gene expression, suggesting dissociation of anorectic and thermogenic effects of leptin, possibly related to chronic cold exposure. Our results indicate that cold-acclimated voles show photoperiod-regulated changes in leptin sensitivity and may provide an attractive model for elucidating molecular mechanisms of leptin resistance.
引用
收藏
页码:153 / 163
页数:11
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