Akirav Eitan M, Chan Owen, Inouye Karen, Riddell Michael C, Matthews Stephen G, Vranic Mladen
Department of Physiology, University of Toronto, Ontraio, Canada.
Metabolism. 2004 Dec;53(12):1558-64. doi: 10.1016/j.metabol.2004.06.024.
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.
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。