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戈德布拉特高血压大鼠中的血管紧张素II与肾功能储备

Angiotensin II and renal functional reserve in rats with Goldblatt hypertension.

作者信息

De Nicola L, Keiser J A, Blantz R C, Gabbai F B

机构信息

Division of Nephrology-Hypertension, University of California, San Diego School of Medicine.

出版信息

Hypertension. 1992 Jun;19(6 Pt 2):790-4. doi: 10.1161/01.hyp.19.6.790.

Abstract

We have previously demonstrated that loss of renal functional reserve (renal response to protein loading) in two-kidney, one clip Goldblatt hypertension is characterized by no change in glomerular filtration rate or single nephron glomerular filtration rate and decreased absolute proximal tubular reabsorption during glycine administration. Captopril restores proximal reabsorption and renal functional reserve in this condition. Because captopril suppresses angiotensin II generation and increases bradykinin, prostaglandins, and potentially nitric oxide, we have investigated the role of angiotensin II blockade in restoring proximal reabsorption and renal functional reserve by comparing captopril with DuP 753, an angiotensin II receptor antagonist, in Goldblatt rats. One month after clipping, two period micropuncture studies (control and glycine) were performed on the unclipped kidney. Normal rats and three groups of clipped rats were studied: an untreated group (HYP), a group treated with captopril (CEI), and a group treated with DuP 753 (DuP) 5 days before micropuncture. Glycine increased glomerular filtration rate, nephron plasma flow, and single nephron glomerular filtration rate in normal rats. Systemic and glomerular hypertension in HYP rats was associated with loss of renal functional reserve and a decrease in absolute proximal reabsorption during glycine. Captopril and DuP 753 normalized systemic and glomerular capillary pressure and prevented the decrease in proximal reabsorption during glycine; however, only CEI rats increased single nephron glomerular filtration rate and glomerular filtration rate after glycine. In conclusion, abnormal responses of both glomerular and tubular function are responsible for the loss of renal functional reserve in Goldblatt rats. Inhibitory angiotensin II activity is responsible for decreasing proximal reabsorption during glycine; however, factors other than angiotensin II limit the glomerular response to glycine.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们先前已证明,在两肾一夹型戈德布拉特高血压模型中,肾功能性储备(肾脏对蛋白质负荷的反应)丧失的特征是,在给予甘氨酸期间,肾小球滤过率或单个肾单位肾小球滤过率无变化,而绝对近端肾小管重吸收减少。卡托普利可恢复此状态下的近端重吸收和肾功能性储备。由于卡托普利可抑制血管紧张素II生成并增加缓激肽、前列腺素以及可能还有一氧化氮,我们通过在戈德布拉特大鼠中比较卡托普利与血管紧张素II受体拮抗剂杜普753,研究了血管紧张素II阻断在恢复近端重吸收和肾功能性储备中的作用。夹闭一个月后,对未夹闭的肾脏进行了两期微穿刺研究(对照和甘氨酸)。研究了正常大鼠和三组夹闭大鼠:未治疗组(HYP)、微穿刺前5天接受卡托普利治疗的组(CEI)和接受杜普753治疗的组(DuP)。甘氨酸可增加正常大鼠的肾小球滤过率、肾单位血浆流量和单个肾单位肾小球滤过率。HYP大鼠的全身性和肾小球性高血压与肾功能性储备丧失以及给予甘氨酸期间绝对近端重吸收减少有关。卡托普利和杜普753使全身性和肾小球毛细血管压力正常化,并防止了给予甘氨酸期间近端重吸收的减少;然而,只有CEI组大鼠在给予甘氨酸后增加了单个肾单位肾小球滤过率和肾小球滤过率。总之,肾小球和肾小管功能的异常反应是戈德布拉特大鼠肾功能性储备丧失的原因。抑制性血管紧张素II活性是导致给予甘氨酸期间近端重吸收减少的原因;然而,血管紧张素II以外的因素限制了肾小球对甘氨酸的反应。(摘要截短于250字)

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