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在恶性易中风自发性高血压大鼠中使用卡托普利、SQ29852、肼屈嗪和33%鱼粉饮食进行长期治疗。

Chronic treatment with captopril, SQ29,852, hydralazine and a 33% fish meal diet in malignant stroke-prone spontaneously hypertensive rats.

作者信息

Okamoto K, Ohta Y, Chikugo T, Shiokawa H, Morita N

机构信息

Department of First Pathology, Kinki University School of Medicine, Osaka, Japan.

出版信息

J Hypertens. 1991 Dec;9(12):1105-17.

PMID:1663966
Abstract

Malignant stroke-prone spontaneously hypertensive rats (M-SHRSP) are a useful animal model for studying juvenile malignant hypertension. Using M-SHRSP males, the effects of SQ 29,852 [(S)-1-[6-amino-2-[[hydroxy (4-phenylbutyl) phosphinyl]oxy]-1-oxohexyl]-L-proline; 30-40 mg/kg per day], captopril (30-40 mg/kg per day), hydralazine hydrochloride (10-15 mg/kg per day) and a 33% fish meal diet on the prevention and therapy of malignant hypertension were examined. Drugs and diet were given separately, beginning at weaning, maturity or adulthood. Observed effects included antihypertension, prolonged life span and prevention and/or reversal of angionecrosis. Each treatment resulted in an antihypertensive effect, but some adult rats seemed treatment-resistant. SQ 29,852 was the most effective treatment for reducing blood pressure. The life span of animals in the treated groups was extended significantly beyond that of the controls. In particular, those rats treated with either captopril or SQ 29,852 lived in excess of 500 days. This included not only those in which treatment resulted in a lowering of blood pressure, but also those whose severe hypertension was not so reduced. Angionecrosis was observed in the organs of many of the non-treated animals, including the brain, heart, kidneys and testes. Both hydralazine and the fish meal diet had a limited effect, if any, on the prevention or reversal of angionecrosis. In contrast, almost none of the rats given either captopril or SQ 29,852 showed cerebrovascular lesions or angionecrosis of the brain, heart and kidneys; angionecrosis in adult M-SHRSP kidneys disappeared within 10 or 18 days after the initiation of SQ 29,852 or captopril, respectively. This data seems to support a possible role for these two drugs not only in prevention, but also in repair, of angionecrosis independent of markedly high blood pressure in M-SHRSP. Based on our overall observations, SQ 29,852 was seen as the most effective of the treatments studied.

摘要

恶性中风倾向自发性高血压大鼠(M-SHRSP)是研究青少年恶性高血压的一种有用动物模型。使用雄性M-SHRSP,研究了SQ 29852[(S)-1-[6-氨基-2-[[羟基(4-苯基丁基)膦酰基]氧基]-1-氧代己基]-L-脯氨酸;每天30 - 40毫克/千克]、卡托普利(每天30 - 40毫克/千克)、盐酸肼屈嗪(每天10 - 15毫克/千克)和33%鱼粉饮食对恶性高血压的预防和治疗作用。药物和饮食从断奶、成熟或成年开始分别给予。观察到的效果包括降压、延长寿命以及预防和/或逆转血管坏死。每种治疗都产生了降压效果,但一些成年大鼠似乎对治疗有抗性。SQ 29852是降低血压最有效的治疗方法。治疗组动物的寿命显著延长,超过了对照组。特别是,那些用卡托普利或SQ 29852治疗的大鼠存活超过500天。这不仅包括治疗后血压降低的大鼠,还包括严重高血压未得到如此降低的大鼠。在许多未治疗动物的器官中观察到血管坏死,包括脑、心脏、肾脏和睾丸。肼屈嗪和鱼粉饮食对血管坏死的预防或逆转作用有限(如果有的话)。相比之下,给予卡托普利或SQ 29852的大鼠几乎没有出现脑血管病变或脑、心脏和肾脏的血管坏死;成年M-SHRSP肾脏中的血管坏死在分别开始给予SQ 29852或卡托普利后10天或18天内消失。这些数据似乎支持这两种药物不仅在预防而且在修复M-SHRSP血管坏死方面可能发挥的作用,这种作用独立于明显的高血压。基于我们的总体观察,SQ 29852被认为是所研究治疗方法中最有效的。

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