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首页> 外文期刊>Metabolism: Clinical and Experimental >Partial leptin restoration increases hypothalamic-pituitary-adrenal activity while diminishing weight loss and hyperphagia in streptozotocin diabetic rats.
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Partial leptin restoration increases hypothalamic-pituitary-adrenal activity while diminishing weight loss and hyperphagia in streptozotocin diabetic rats.

机译:瘦素的部分恢复可增加链脲佐菌素糖尿病大鼠的下丘脑-垂体-肾上腺活性,同时减少体重减轻和食欲亢进。

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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.
机译:长期服用瘦素的药理剂量可使链脲佐菌素(STZ)糖尿病大鼠的食物摄入和体重正常化。我们通过使用皮下渗透微型泵检查了STZ糖尿病大鼠急性部分生理瘦素恢复的代谢作用。组:(1)大鼠注入媒介物(DV); (2)以4.5微克的剂量注入重组鼠甲硫氨酸瘦素(DL)的大鼠。 (kg体重.d)(-1); (3)成对喂食的大鼠(DP)的食物定量与DL组所消耗的食物定量相匹配。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大鼠的食物消耗量显着低于DV大鼠。矛盾的是,尽管食物摄入量与DP组相似,但体重却降低了40%,但DL大鼠的初始体重却增加了约20%(P <.05)。与N,DP和DV大鼠相比,DL大鼠的血浆皮质激素和ACTH浓度升高了2倍至3倍。在远端部,与N和DV大鼠相比,DL和DP大鼠的糖皮质激素受体(GR)mRNA水平明显更高。我们的结果表明生理瘦素的部分恢复:(1)成功减轻食欲亢进,同时使STZ糖尿病大鼠体重增加; (2)增加STZ糖尿病大鼠的皮质酮水平,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 mRNA水平升高有关,这表明瘦素可能会干扰HPA轴的负反馈调节。

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