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部分瘦素恢复可增加链脲佐菌素诱导的糖尿病大鼠下丘脑-垂体-肾上腺的活性,同时减少体重减轻和食欲亢进。

Partial leptin restoration increases hypothalamic-pituitary-adrenal activity while diminishing weight loss and hyperphagia in streptozotocin diabetic rats.

作者信息

Akirav Eitan M, Chan Owen, Inouye Karen, Riddell Michael C, Matthews Stephen G, Vranic Mladen

机构信息

Department of Physiology, University of Toronto, Ontraio, Canada.

出版信息

Metabolism. 2004 Dec;53(12):1558-64. doi: 10.1016/j.metabol.2004.06.024.

Abstract

Chronic leptin administration at pharmacologic doses normalizes food intake and body weight in streptozotocin (STZ)-diabetic rats. We examined the metabolic effects of acute partial physiological leptin restoration in STZ-diabetic rats by using subcutaneous osmotic mini pumps. Groups: (1) Rats infused with vehicle (DV); (2) rats infused with recombinant murine methionine leptin (DL) at 4.5 microg . (kg body weight . d)(-1); (3)pair-fed rats (DP) given a food ration matching that consumed by the DL group. A fourth group of nondiabetic, normal (N) rats was also studied to assess normal metabolic efficiency, hypothalamic-pituitary-adrenal (HPA) activity and sympathoadrenal activity. Following leptin infusion, food consumption by DL rats was significantly lower than in DV rats. Paradoxically, despite a similar food intake to that of the DP group, which demonstrated a 40% reduction in body mass, DL rats increased their initial body weight by approximately 20% (P < .05). Plasma corticosterone and ACTH concentrations were elevated by 2-fold to 3-fold in DL versus N, DP, and DV rats. In the pars distalis, glucocorticoid receptor (GR) mRNA levels were significantly higher in DL and DP rats compared with N and DV rats. Our results suggest that partial restoration of physiologic leptin: (1) successfully reduces hyperphagia while allowing body weight gain in STZ-diabetic rats; (2) increases corticosterone levels in STZ-diabetic rats, which may in turn counteract the anorexic effects of diabetes; and (3) is associated with increased pituitary GR mRNA levels, despite elevated corticosterone levels, suggesting that leptin may interfere with the negative feedback regulation of the HPA axis.

摘要

以药理剂量长期给予瘦素可使链脲佐菌素(STZ)诱导的糖尿病大鼠的食物摄入量和体重恢复正常。我们通过皮下渗透微型泵研究了急性部分生理性瘦素恢复对STZ糖尿病大鼠的代谢影响。分组:(1)输注赋形剂的大鼠(DV);(2)以4.5微克·(千克体重·天)-1的剂量输注重组鼠蛋氨酸瘦素的大鼠(DL);(3)配对喂养的大鼠(DP),给予与DL组消耗的食物量相匹配的食物定量。还研究了第四组非糖尿病正常(N)大鼠,以评估正常的代谢效率、下丘脑-垂体-肾上腺(HPA)活性和交感肾上腺活性。瘦素输注后,DL组大鼠的食物消耗量显著低于DV组大鼠。矛盾的是,尽管DL组大鼠的食物摄入量与DP组相似(DP组体重降低了40%),但其初始体重却增加了约20%(P<0.05)。与N、DP和DV组大鼠相比,DL组大鼠的血浆皮质酮和促肾上腺皮质激素(ACTH)浓度升高了2至3倍。在垂体远侧部,与N和DV组大鼠相比,DL和DP组大鼠糖皮质激素受体(GR)的mRNA水平显著更高。我们的结果表明,生理性瘦素的部分恢复:(1)成功减少了STZ糖尿病大鼠的食欲过盛,同时使其体重增加;(2)增加了STZ糖尿病大鼠的皮质酮水平,这可能反过来抵消糖尿病的厌食作用;(3)尽管皮质酮水平升高,但与垂体GR的mRNA水平增加有关,这表明瘦素可能干扰HPA轴的负反馈调节。

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