Blunted metabolic response to fasting in obese mice

被引:17
作者
Ueno, Naohiko [1 ]
Asakawa, Akihiro [2 ]
Inui, Akio [2 ]
机构
[1] Kobe Seaside Hosp, Dept Internal Med, Chuo Ku, Kobe, Hyogo 6510084, Japan
[2] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Social & Behav Med, Div Behav Med, Kagoshima, Japan
关键词
obese mice; fasting; ghrelin; oxygen consumption;
D O I
10.1007/s12020-007-9016-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of the study was to evaluate metabolic changes in response to fasting in normal and obese mice. C57BL6 and obese (diet-induced obesity (DIO) and ob/ob) mice were used in this study. They were fasted for 24 h and re-fed for 24 h. Body weight was monitored before, after fasting and during re-feeding (2 and 24 h after re-feeding). Food intake was measured 2 and 24 h after re-feeding began. Blood samples were taken before and after 24 h fasting. As metabolic parameters, blood glucose, plasma insulin, ghrelin levels and oxygen consumption were measured. Blood glucose and plasma insulin levels in DIO and ob/ob mice were higher than normal mice, and plasma ghrelin levels were lower in DIO and ob/ob mice. There was reduced body weight loss in DIO mice than in normal mice for 24 h fasting. When they were re-fed, DIO and ob/ob mice consumed less food intake than normal mice. Twenty-four hours food deprivation induced significantly smaller plasma ghrelin elevation in these obese mice. Fasting-induced decrease in oxygen consumption was significantly smaller in DIO and ob/ob mice than normal mice. This data show that obese mice may have decreased sensitivity to fasting-induced increase in circulating ghrelin and their oxygen consumption exhibited a blunted response to fasting.
引用
收藏
页码:192 / 196
页数:5
相关论文
共 15 条
[1]   Delayed short-term secretory regulation of ghrelin in obese animals: Evidenced by a specific RIA for the active form of ghrelin [J].
Ariyasu, H ;
Takaya, K ;
Hosoda, H ;
Iwakura, H ;
Ebihara, K ;
Mori, K ;
Ogawa, Y ;
Hosoda, K ;
Akamizu, T ;
Kojima, M ;
Kangawa, K ;
Nakao, K .
ENDOCRINOLOGY, 2002, 143 (09) :3341-3350
[2]   Ghrelin is an appetite-stimulatory signal from stomach with structural resemblance to motilin [J].
Asakawa, A ;
Inui, A ;
Kaga, T ;
Yuzuriha, H ;
Nagata, T ;
Ueno, N ;
Makino, S ;
Fujimiya, M ;
Niijima, A ;
Fujino, MA ;
Kasuga, M .
GASTROENTEROLOGY, 2001, 120 (02) :337-345
[3]   A preprandial rise in plasma ghrelin levels suggests a role in meal initiation in humans [J].
Cummings, DE ;
Purnell, JQ ;
Frayo, RS ;
Schmidova, K ;
Wisse, BE ;
Weigle, DS .
DIABETES, 2001, 50 (08) :1714-1719
[4]   Starvation: Early signals, sensors, and sequelae [J].
Dallman, MF ;
Akana, SF ;
Bhatnagar, S ;
Bell, ME ;
Choi, S ;
Chu, A ;
Horsley, C ;
Levin, N ;
Meijer, O ;
Soriano, LR ;
Strack, AM ;
Viau, V .
ENDOCRINOLOGY, 1999, 140 (09) :4015-4023
[5]   Food fails to suppress ghrelin levels in obese humans [J].
English, PJ ;
Ghatei, MA ;
Malik, IA ;
Bloom, SR ;
Wilding, JPH .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (06) :2984-2987
[6]   The influence of insulin on circulating ghrelin [J].
Flanagan, DE ;
Evans, ML ;
Monsod, TP ;
Rife, F ;
Heptulla, RA ;
Tamborlane, WV ;
Sherwin, RS .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 284 (02) :E313-E316
[7]   Circulating ghrelin concentrations are lowered by intravenous glucose or hyperinsulinemic euglycemic conditions in rodents [J].
McCowen, KC ;
Maykel, JA ;
Bistrian, BR ;
Ling, PR .
JOURNAL OF ENDOCRINOLOGY, 2002, 175 (02) :R7-R11
[8]   Resistance to the orexigenic effect of ghrelin in dietary-induced obesity in mice: reversal upon weight loss [J].
Perreault, M ;
Istrate, N ;
Wang, L ;
Nichols, AJ ;
Tozzo, E ;
Stricker-Krongrad, A .
INTERNATIONAL JOURNAL OF OBESITY, 2004, 28 (07) :879-885
[9]   Low plasma ghrelin is associated with insulin resistance, hypertension, and the prevalence of type 2 diabetes [J].
Pöykkö, SM ;
Kellokoski, E ;
Hörkkö, S ;
Kauma, H ;
Kesäniemi, YA ;
Ukkola, O .
DIABETES, 2003, 52 (10) :2546-2553
[10]   Ghrelin levels correlate with insulin levels, insulin resistance, and high-density lipoprotein cholesterol, but not with gender, menopausal status, or cortisol levels in humans [J].
Purnell, JQ ;
Weigle, DS ;
Breen, P ;
Cummings, DE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (12) :5747-5752