Department of Biomedical Sciences and Program in Neuroscience, College of Medicine, Florida State University, Tallahassee, FL 32306, USA.
Int J Obes (Lond). 2011 Sep;35(9):1183-92. doi: 10.1038/ijo.2010.262. Epub 2010 Dec 21.
To examine the cardiovascular effects of combined amylin (AMN) and leptin (LEP) treatment in lean and obese rats.
Rats were instrumented for telemetry and given LEP (300 μg kg(-1) day(-1)), AMN (100 μg kg(-1) day(-1)), AMN+LEP or vehicle (VEH; 0.9% normal saline) via a subcutaneous mini-osmotic pump for 7 days. The VEH group was subdivided into ad libitum fed and pair-fed to the amount of food AMN+LEP animals ate daily. Rats were housed in metabolic chambers for analysis of cardiovascular physiology and metabolism.
Male Fisher 344 × Brown Norway (FBNF1; Harlan; age=3-5 months; n=72) rats were placed on standard rodent chow (LEAN, n=41) or moderately high-fat diet (OBESE; n=31) to produce obesity.
AMN+LEP potently reduced food intake (LEAN: 57% OBESE: 59%) and abdominal fat mass (LEAN: 56% OBESE: 41%). Pair-fed rats displayed bradycardia and metabolic suppression. In contrast, AMN+LEP increased heart rate and oxygen consumption above levels in LEP or AMN-treated rats. LEP reduced blood pressure in both lean and obese rats but AMN had no effect. LEP-induced reductions in blood pressure were not altered by AMN+LEP treatment. Thus, AMN+LEP treatment decreased food intake, body fat and blood pressure in lean and obese rats.
We conclude that the potent anti-adiposity actions of AMN+LEP are due in part to prevention of the bradycardia and metabolic suppression typically observed with negative energy balance. Furthermore, the hypotensive actions of peripheral LEP treatment are observable in spite of the potent AMN+LEP activation of anorexic and thermogenic mechanisms in the central nervous system.
研究胰淀素(AMN)和瘦素(LEP)联合治疗对瘦鼠和肥胖鼠心血管的影响。
通过皮下微量渗透泵给大鼠输注 LEP(300μg/kg/天)、AMN(100μg/kg/天)、AMN+LEP 或载体(VEH;0.9%生理盐水),持续 7 天。VEH 组再分为自由进食和按 AMN+LEP 组大鼠每日进食量进行限食。将大鼠饲养在代谢室中以分析心血管生理学和代谢。
雄性 Fisher 344×Brown Norway(FBNF1;Harlan;年龄 3-5 个月;n=72)大鼠,分为标准啮齿动物饲料喂养(LEAN,n=41)或适度高脂肪饮食喂养(OBESE,n=31)以诱导肥胖。
AMN+LEP 显著减少进食量(LEAN:57%;OBESE:59%)和腹部脂肪量(LEAN:56%;OBESE:41%)。限食大鼠显示心动过缓和代谢抑制。相反,AMN+LEP 使心率和耗氧量高于 LEP 或 AMN 处理的大鼠。LEP 降低了 lean 和 obese 两组大鼠的血压,但 AMN 没有影响。LEP 诱导的血压降低不受 AMN+LEP 治疗的影响。因此,AMN+LEP 治疗降低了 lean 和 obese 两组大鼠的进食量、体脂肪和血压。
我们得出结论,AMN+LEP 的强大抗肥胖作用部分归因于预防与负能平衡相关的心动过缓和代谢抑制。此外,尽管 AMN+LEP 强烈激活中枢神经系统的厌食和产热机制,但外周 LEP 治疗的降压作用仍可观察到。