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肥胖、胰岛素抵抗犬对慢性高胰岛素血症的血流动力学和肾脏反应。

Hemodynamic and renal responses to chronic hyperinsulinemia in obese, insulin-resistant dogs.

作者信息

Hall J E, Brands M W, Zappe D H, Dixon W N, Mizelle H L, Reinhart G A, Hildebrandt D A

机构信息

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

出版信息

Hypertension. 1995 May;25(5):994-1002. doi: 10.1161/01.hyp.25.5.994.

Abstract

We previously reported that chronic hyperinsulinemia does not cause hypertension in normal insulin-sensitive dogs. However, resistance to the metabolic and vasodilator effects of insulin may be a prerequisite for hyperinsulinemia to elevate blood pressure. The present study tested this hypothesis by comparing the control of systemic hemodynamics and renal function during chronic hyperinsulinemia in instrumented normal conscious dogs (n = 6) and in dogs made obese and insulin resistant by feeding them a high-fat diet for 6 weeks (n = 6). After 6 weeks of the high-fat diet, body weight increased from 24.0 +/- 1.2 to 40.9 +/- 1.2 kg, arterial pressure rose from 83 +/- 5 to 106 +/- 4 mm Hg, and cardiac output rose from 2.98 +/- 0.29 to 5.27 +/- 0.54 L/min. Insulin sensitivity, assessed by fasting hyperinsulinemia and by the hyperinsulinemic euglycemic clamp technique, was markedly reduced in obese dogs. Insulin infusion (1.0 mU/kg per minute for 7 days) in obese dogs elevated plasma insulin from 42 +/- 12 microU/mL to 95 to 219 microU/mL but failed to increase arterial pressure, which averaged 106 +/- 4 mm Hg during control and 102 +/- 4 mm Hg during 7 days of insulin infusion. Hyperinsulinemia for 7 days in obese dogs elevated heart rate from 116 +/- 8 to 135 +/- 7 beats per minute but caused no significant changes in cardiac output, in contrast to normal dogs (n = 6), in which marked increases in cardiac output (31 +/- 5% after 7 days) and decreases in total peripheral resistance occurred during chronic insulin infusion.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们之前报道过,慢性高胰岛素血症不会在正常胰岛素敏感的犬类中引发高血压。然而,对胰岛素的代谢和血管舒张作用产生抵抗可能是高胰岛素血症升高血压的一个先决条件。本研究通过比较植入仪器的正常清醒犬(n = 6)和通过喂食高脂饮食6周使其肥胖且胰岛素抵抗的犬(n = 6)在慢性高胰岛素血症期间的全身血流动力学和肾功能控制情况,来检验这一假设。高脂饮食6周后,体重从24.0±1.2千克增加到40.9±1.2千克,动脉压从83±5毫米汞柱升至106±4毫米汞柱,心输出量从2.98±0.29升/分钟升至5.27±0.54升/分钟。通过空腹高胰岛素血症和高胰岛素正常血糖钳夹技术评估的胰岛素敏感性在肥胖犬中显著降低。肥胖犬中胰岛素输注(1.0微单位/千克每分钟,持续7天)使血浆胰岛素从42±12微单位/毫升升至95至219微单位/毫升,但未能增加动脉压,对照期间平均动脉压为106±4毫米汞柱,胰岛素输注7天期间为102±4毫米汞柱。肥胖犬中7天的高胰岛素血症使心率从116±8次/分钟升至135±7次/分钟,但心输出量无显著变化,这与正常犬(n = 6)相反,正常犬在慢性胰岛素输注期间心输出量显著增加(7天后增加31±5%)且总外周阻力降低。(摘要截短至250字)

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