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高钾饮食可降低易中风自发性高血压大鼠的脑出血、梗死、死亡率和肠系膜小动脉肥厚。

High-K diets reduce brain haemorrhage and infarcts, death rate and mesenteric arteriolar hypertrophy in stroke-prone spontaneously hypertensive rats.

作者信息

Tobian L, Lange J M, Johnson M A, MacNeill D A, Wilke T J, Ulm K M, Wold L J

出版信息

J Hypertens Suppl. 1986 Dec;4(5):S205-7.

PMID:3471904
Abstract

Male stroke-prone spontaneously hypertensive rats (SHRSP) were fed 4% NaCl diets containing either 0.75% normal K or 2.11% high K, starting at 6 weeks of age. After 8 months on these diets 69% of 58 SHRSP rats on 0.75% K had died, whereas 2% of 95 rats of 2.11% K died, a 98% reduction in mortality, P less than 0.000 001. After 20 weeks the daytime and night-time blood pressure (BP) of each rat were measured intra-arterially. We selected two groups precisely matched for BP. One matched SHRSP group (BP 182 mmHg) ate the 0.75% K diet and 30 of 47 rats died (64% mortality). The other matched SHRSP group (BP 182 mmHg) ate the 2.11% K diet, and two of 35 died (6% mortality, a 91% reduction of mortality, P less than 0.0001). Seemingly, the striking reduction in mortality rate with the 2.11% hig-K diet does not depend on a lowering of BP. High-K diets do not change body Na or K. The dry weight of mesenteric arterioles was reduced by 22% on 2.11% K diet versus 75% K (7.5 versus 9.7 mg) (P less than 0.001), indicating a greatly reduced hypertensive hypertrophy. In nine surviving SHRSP on 0.75% K, 13 of 36 brain hemisphere slides (four slides per rat) showed infarcts (36%). In 11 surviving SHRSP on 2.11% K, one of 44 brain slides showed infarcts (2%, a 94.5% reduction, P less than 0.0001). Brain haemorrhage was reduced by 92% on the 2.11% K diet. High-K diets allow cerebral arteries to carry very high BPs without sustaining damage to the artery wall, thereby drastically reducing brain infarcts and lowering the death rate.

摘要

雄性易中风自发性高血压大鼠(SHRSP)从6周龄开始喂食含0.75%正常钾或2.11%高钾的4%氯化钠饮食。在这些饮食喂养8个月后,58只食用0.75%钾饮食的SHRSP大鼠中有69%死亡,而95只食用2.11%钾饮食的大鼠中只有2%死亡,死亡率降低了98%,P<0.000001。20周后,通过动脉内测量每只大鼠的白天和夜间血压(BP)。我们选择了两组血压精确匹配的大鼠。一组匹配的SHRSP组(血压182mmHg)食用0.75%钾饮食,47只大鼠中有30只死亡(死亡率64%)。另一组匹配的SHRSP组(血压182mmHg)食用2.11%钾饮食,35只大鼠中有2只死亡(死亡率6%,死亡率降低了91%,P<0.0001)。显然,2.11%高钾饮食导致的死亡率显著降低并不依赖于血压的降低。高钾饮食不会改变体内的钠或钾含量。与75%钾饮食相比,2.11%钾饮食使肠系膜小动脉的干重减少了22%(分别为7.5mg和9.7mg)(P<0.001),表明高血压性肥大明显减轻。在9只存活的食用0.75%钾饮食的SHRSP大鼠中,36个脑半球切片(每只大鼠4个切片)中有13个显示梗死(36%)。在11只存活的食用2.11%钾饮食的SHRSP大鼠中,44个脑切片中有1个显示梗死(2%,降低了94.5%,P<0.0001)。2.11%钾饮食使脑出血减少了92%。高钾饮食使脑动脉能够承受非常高的血压而不会对动脉壁造成损伤,从而大幅减少脑梗死并降低死亡率。

相似文献

1
High-K diets reduce brain haemorrhage and infarcts, death rate and mesenteric arteriolar hypertrophy in stroke-prone spontaneously hypertensive rats.高钾饮食可降低易中风自发性高血压大鼠的脑出血、梗死、死亡率和肠系膜小动脉肥厚。
J Hypertens Suppl. 1986 Dec;4(5):S205-7.
2
High-potassium diets markedly protect against stroke deaths and kidney disease in hypertensive rats, an echo from prehistoric days.高钾饮食能显著预防高血压大鼠的中风死亡和肾脏疾病,这是来自史前时代的一个呼应。
J Hypertens Suppl. 1986 Oct;4(4):S67-76.
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High potassium diets markedly protect against stroke deaths and kidney disease in hypertensive rats, a possible legacy from prehistoric times.高钾饮食能显著预防高血压大鼠的中风死亡和肾脏疾病,这可能是史前时代遗留下来的。
Can J Physiol Pharmacol. 1986 Jun;64(6):840-8. doi: 10.1139/y86-145.
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The effects of dietary sodium on hypertension and stroke development in female stroke-prone spontaneously hypertensive rats.膳食钠对易患中风的雌性自发性高血压大鼠的高血压及中风发展的影响。
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Potassium prevents death from strokes in hypertensive rats without lowering blood pressure.钾可预防高血压大鼠中风致死,且不降低血压。
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Na+/K+-ATPase alpha isoforms expression in stroke-prone spontaneously hypertensive rat heart ventricles: effect of salt loading and lacidipine treatment.钠钾ATP酶α亚型在易患中风自发性高血压大鼠心室中的表达:盐负荷和拉西地平治疗的影响。
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Renal function in stroke-prone rats fed a high-K+ diet.喂食高钾饮食的易中风大鼠的肾功能。
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Dietary prevention of stroke and its mechanisms in stroke-prone spontaneously hypertensive rats--preventive effect of dietary fibre and palmitoleic acid.易患中风的自发性高血压大鼠中风的饮食预防及其机制——膳食纤维和棕榈油酸的预防作用
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Prevention of stroke with perindopril treatment in stroke-prone spontaneously hypertensive rats.培哚普利治疗对易卒中自发性高血压大鼠卒中的预防作用
Clin Invest Med. 1997 Oct;20(5):327-38.

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