Daily melatonin administration at middle age suppresses male rat visceral fat, plasma leptin, and plasma insulin to youthful levels

被引:216
作者
Rasmussen, DD [1 ]
Boldt, BM
Wilkinson, CW
Yellon, SM
Matsumoto, AM
机构
[1] Univ Washington, VA Puget Sound Hlth Care Syst, Mental Hlth Serv, Seattle, WA 98195 USA
[2] Univ Washington, VA Puget Sound Hlth Care Syst, Ctr Geriatr Res Educ & Clin, Seattle, WA 98195 USA
[3] Univ Washington, Dept Med, Seattle, WA 98195 USA
[4] Univ Washington, Dept Psychiat, Seattle, WA 98195 USA
[5] Loma Linda Univ, Dept Physiol, Loma Linda, CA 92350 USA
关键词
D O I
10.1210/en.140.2.1009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Human and rat pineal melatonin secretion decline with aging, whereas visceral fat and plasma insulin levels increase. Melatonin modulates fat metabolism in some mammalian species, so these aging-associated melatonin, fat and insulin changes could be functionally related. Accordingly, we investigated the effects of daily melatonin supplementation to male Sprague-Dawley rats, starting at middle age (10 months) and continuing into old age (22 months). Melatonin was added to the drinking water (92% of which was consumed at night) at a dosage (4 mu g/ml) previously reported to attenuate the aging-associated decrease in survival rate in male rats, as well as at a 10-fold lower dosage. The higher dosage produced nocturnal plasma melatonin levels in middle-aged rats which were 15-fold higher than in young (4 months) rats; nocturnal plasma melatonin levels in middle-aged rats receiving the lower dosage were not significantly different from young or middle-aged controls, Relative (% of body wt) retroperitoneal and epididymal fat, as well as plasma insulin and leptin levels, were all significantly increased at middle age when compared to young rats. All were restored within 10 weeks to youthful (4 month) levels in response to both dosages of melatonin. Continued treatment until old age maintained suppression of visceral (retroperitoneal + epididymal) fat levels. Plasma corticosterone and total thyroxine (T4) levels were not significantly altered by aging or melatonin treatment. Plasma testosterone, insulin-like growth factor 1 (IGF-1) and total triiodothyronine (T3) decreased by middle age; these aging-associated decreases were not significantly altered by melatonin treatment. Thus, visceral fat, insulin and leptin responses to melatonin administration may be independent of marked changes in gonadal, thyroid, adrenal or somatotropin regulation. Since increased visceral fat is associated with increased insulin resistance, diabetes, and cardiovascular disease, these results suggest that appropriate melatonin supplementation may potentially provide prophylaxis or therapy for some prominent pathologies associated with aging.
引用
收藏
页码:1009 / 1012
页数:4
相关论文
共 14 条
[1]   Caloric restriction reverses hepatic insulin resistance in aging rats by decreasing visceral fat [J].
Barzilai, N ;
Banerjee, S ;
Hawkins, M ;
Chen, W ;
Rossetti, L .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (07) :1353-1361
[2]   Melatonin in relation to physiology in adult humans [J].
Cagnacci, A .
JOURNAL OF PINEAL RESEARCH, 1996, 21 (04) :200-213
[3]  
DESPRES JP, 1993, NUTRITION, V9, P452
[4]   THE ROLE OF MELATONIN AND SEROTONIN IN AGING - UPDATE [J].
GRAD, BR ;
ROZENCWAIG, R .
PSYCHONEUROENDOCRINOLOGY, 1993, 18 (04) :283-295
[5]   Role of melatonin in mediating seasonal energetic and immunologic adaptations [J].
Nelson, RJ ;
Demas, GE .
BRAIN RESEARCH BULLETIN, 1997, 44 (04) :423-430
[6]   EFFECTS OF LONG-TERM ADMINISTRATION OF MELATONIN AND A PUTATIVE ANTAGONIST ON THE AGING RAT [J].
OAKNINBENDAHAN, S ;
ANIS, Y ;
NIR, I ;
ZISAPEL, N .
NEUROREPORT, 1995, 6 (05) :785-788
[7]   FLUCTUATION OF BLOOD MELATONIN CONCENTRATIONS WITH AGE - RESULT OF CHANGES IN PINEAL MELATONIN SECRETION, BODY GROWTH, AND AGING [J].
PANG, SF ;
TSANG, CW ;
HONG, GX ;
YIP, PCY ;
TANG, PL ;
BROWN, GM .
JOURNAL OF PINEAL RESEARCH, 1990, 8 (02) :179-192
[8]  
PESCHKE D, 1987, NEUROENDOCRINOL LETT, V9, P321
[9]   Acute alcohol effects on opiomelanocortinergic regulation [J].
Rasmussen, DD ;
Bryant, CA ;
Boldt, BM ;
Colasurdo, EA ;
Levin, N ;
Wilkinson, CW .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1998, 22 (04) :789-801
[10]   STUDIES IN THE DISTRIBUTION OF BODY-FAT .1. EFFECTS OF AGE, SEX, AND OBESITY [J].
SHIMOKATA, H ;
TOBIN, JD ;
MULLER, DC ;
ELAHI, D ;
COON, PJ ;
ANDRES, R .
JOURNALS OF GERONTOLOGY, 1989, 44 (02) :M66-M75