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高脂饮食喂养的大鼠中,中枢性瘦素输注引起的慢性血压和食欲反应。

Chronic blood pressure and appetite responses to central leptin infusion in rats fed a high fat diet.

机构信息

Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi 39216-4505, USA.

出版信息

J Hypertens. 2011 Apr;29(4):758-62. doi: 10.1097/HJH.0b013e328344280b.

Abstract

OBJECTIVE

Obesity has been suggested to induce selective leptin resistance whereby leptin's anorexic effects are attenuated, whereas the effects to increase sympathetic nervous system activity and blood pressure remain intact. Most studies, however, have tested only the acute responses to leptin administration. This study tested whether feeding a high-fat diet causes resistance to the appetite and cardiovascular responses to chronic central leptin infusion.

METHODS

Sprague-Dawley rats were fed high-fat diet (40% kcal from fat, n=5) or normal-fat diet (13% kcal from fat, n=5) for a year. Radiotelemeters were implanted for continuous monitoring of mean arterial pressure (MAP) and heart rate (HR). A 21G steel cannula was implanted in the lateral cerebral ventricle [intracerebroventricular (ICV)]. After recovery, leptin was infused ICV at 0.02 μg/kg per min for 10 days.

RESULTS

High-fat rats were heavier than normal-fat rats (582±12 vs. 511±19 g) and exhibited significantly higher MAP (114±3 vs. 96±7 mmHg). Although the acute (24 h) effects of leptin were attenuated in high-fat rats, chronic ICV leptin infusion decreased caloric intake in both groups similarly (50±8 vs. 40±10%) by day 5. Despite decreased food intake and weight loss, leptin infusion significantly increased MAP and HR in both high-fat and normal-fat rats (7±2 and 5±1 mmHg; 18±11 and 21±10 b.p.m., respectively).

CONCLUSION

These results suggest that obesity induced by feeding a high-fat diet blunts the acute anorexic effects of leptin but does not cause significant resistance to the chronic central nervous system effects of leptin on appetite, MAP, or HR.

摘要

目的

肥胖被认为会导致选择性瘦素抵抗,从而削弱瘦素的厌食作用,而增加交感神经系统活动和血压的作用仍然完好无损。然而,大多数研究仅测试了急性给予瘦素后的反应。本研究测试了高脂饮食是否会导致对慢性中枢性瘦素输注的食欲和心血管反应产生抵抗。

方法

Sprague-Dawley 大鼠喂食高脂肪饮食(40%热量来自脂肪,n=5)或正常脂肪饮食(13%热量来自脂肪,n=5)一年。植入无线电遥测仪以连续监测平均动脉压(MAP)和心率(HR)。在侧脑室内(ICV)植入 21G 钢套管。恢复后,以 0.02μg/kg/min 的速度持续 10 天向 ICV 输注瘦素。

结果

高脂肪组大鼠比正常脂肪组大鼠更重(582±12 比 511±19 g),且 MAP 明显更高(114±3 比 96±7 mmHg)。尽管高脂大鼠的瘦素急性(24 小时)作用减弱,但慢性 ICV 瘦素输注在两组中均使热量摄入相似地减少(50±8 比 40±10%),到第 5 天。尽管食物摄入量减少和体重减轻,瘦素输注仍显著增加了两组大鼠的 MAP 和 HR(7±2 和 5±1 mmHg;18±11 和 21±10 b.p.m.,分别)。

结论

这些结果表明,高脂饮食引起的肥胖会削弱瘦素的急性厌食作用,但不会导致对瘦素对食欲、MAP 或 HR 的慢性中枢神经系统作用产生显著抵抗。

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