中国临床药理学杂志
中國臨床藥理學雜誌
중국림상약이학잡지
THE CHINESE JOURNAL OF CLINICAL PHARMACOLOGY
2015年
7期
501-504
,共4页
陈申杰%叶武%朱敏%陈洁%冯培芳
陳申傑%葉武%硃敏%陳潔%馮培芳
진신걸%협무%주민%진길%풍배방
通心络%自发性高血压大鼠%血管紧张素转化酶2%氨氯地平
通心絡%自髮性高血壓大鼠%血管緊張素轉化酶2%氨氯地平
통심락%자발성고혈압대서%혈관긴장소전화매2%안록지평
Tong Xin Luo%spontaneously hypertensive rats%renal damage%angiotensin-converting enzyme 2%amlodipine
目的:研究通心络对自发性高血压大鼠( SHR )肾损害的干预作用及机制。方法10周龄雄性SHR 48只随机分成5组:SHR对照组(同龄Wistar大鼠作对照),氨氯地平干预组和氨氯地平+不同剂量通心络(0.5,1.0,1.5 g· kg-1· d-1)干预组。20周后,测血压、留尿后处死,取肾组织检测指标。测尿微量白蛋白( UMA)和β2微球蛋白(β2 MG),测血管紧张素转化酶2、血管紧张素Ⅱ1型受体基因表达。结果与同龄京都威斯特( WKY)大鼠比较,10周龄SHR的尿β2 MG、肾组织AT1 R表达明显增加而ACE2明显减少。与单用氨氯地平组比较,伍用通心络组大鼠的尿β2 MG、UMA及肾组织AT1 R表达明显减少而肾组织ACE2表达明显增加。结论氨氯地平伍用通心络能降低蛋白尿、减轻高血压病肾损害的作用可能是通过增加肾组织ACE2、下调AT1 R表达来实现的。
目的:研究通心絡對自髮性高血壓大鼠( SHR )腎損害的榦預作用及機製。方法10週齡雄性SHR 48隻隨機分成5組:SHR對照組(同齡Wistar大鼠作對照),氨氯地平榦預組和氨氯地平+不同劑量通心絡(0.5,1.0,1.5 g· kg-1· d-1)榦預組。20週後,測血壓、留尿後處死,取腎組織檢測指標。測尿微量白蛋白( UMA)和β2微毬蛋白(β2 MG),測血管緊張素轉化酶2、血管緊張素Ⅱ1型受體基因錶達。結果與同齡京都威斯特( WKY)大鼠比較,10週齡SHR的尿β2 MG、腎組織AT1 R錶達明顯增加而ACE2明顯減少。與單用氨氯地平組比較,伍用通心絡組大鼠的尿β2 MG、UMA及腎組織AT1 R錶達明顯減少而腎組織ACE2錶達明顯增加。結論氨氯地平伍用通心絡能降低蛋白尿、減輕高血壓病腎損害的作用可能是通過增加腎組織ACE2、下調AT1 R錶達來實現的。
목적:연구통심락대자발성고혈압대서( SHR )신손해적간예작용급궤제。방법10주령웅성SHR 48지수궤분성5조:SHR대조조(동령Wistar대서작대조),안록지평간예조화안록지평+불동제량통심락(0.5,1.0,1.5 g· kg-1· d-1)간예조。20주후,측혈압、류뇨후처사,취신조직검측지표。측뇨미량백단백( UMA)화β2미구단백(β2 MG),측혈관긴장소전화매2、혈관긴장소Ⅱ1형수체기인표체。결과여동령경도위사특( WKY)대서비교,10주령SHR적뇨β2 MG、신조직AT1 R표체명현증가이ACE2명현감소。여단용안록지평조비교,오용통심락조대서적뇨β2 MG、UMA급신조직AT1 R표체명현감소이신조직ACE2표체명현증가。결론안록지평오용통심락능강저단백뇨、감경고혈압병신손해적작용가능시통과증가신조직ACE2、하조AT1 R표체래실현적。
Objective To explore the effect of Tong Xin Luo ( TXL) on the renal damage by hypertension in spontaneously hypertensive rats ( SHR).Methods Ten week -old male SHR ( n=48 ) were randomly divided into 5 groups:control group , the amlodipine group , the amlodi-pine and different dose TXL groups.The same old male Wistor -Kyoto ( WK) rats was as control group .At the time of 20 weeks later after treatment, blood pressure, urine microalbumin, urine β2 -microglobulin were detected , the gene expression of angiotensin -converting enzyme 2 (ACE2) and angiotensin II type 1 receptor (AT1R) in rats kidney were determined.Results Compared with Wistar -Kyoto ( WKY ) control group, 10 week -old SHR showed higher levels of urine β2 MG and ACE2 , but less AT1 R.After treatment for 20 weeks, compared with the amlodipine group , amlodipine with TXL reduced urinary β2 -microglo-bulin and urine microalbumin , decreased AT 1 R expression and increased ACE2 expression.Conclusion Taking high-dose TXL with antihyper-tensive therapy could prevent renal damage progression , and its effect may be through lowering albuminuria , increasing renal ACE 2 expression , and decreasing AT 1 R expression.