Sharma J N, Fernandez P G, Kim B K, Triggle C R
Can J Physiol Pharmacol. 1984 Jul;62(7):846-9. doi: 10.1139/y84-139.
Systolic blood pressure responses to enalapril maleate (MK 421, a new angiotensin converting enzyme inhibitor (CEI] and hydrochlorothiazide (HTZ) were studied in conscious Dahl salt-sensitive (DS) and salt-resistant (DR) rats maintained on a high salt (8.0% NaCl) and a normal salt (0.4% NaCl) diet. The DS rats were severely hypertensive after 3 weeks on the high salt diet whereas the systolic blood pressure (SBP) of the DR rats were normotensive. Oral treatment with enalapril (15-100 mg X kg-1 X day-1) and HTZ (60-400 mg X kg-1 X day-1) caused a significant reduction of SBP in the DS rats with the high salt diet (P less than 0.001); however, this was not observed until after 4 weeks of treatment when the dosage was 30 and 150 mg X kg-1 X day-1, respectively. Furthermore, enalapril therapy alone significantly reduced the SBP of all groups of rats regardless of diet or Dahl strain (P less than 0.001), but this was not observed until the end of the 7th week of therapy in DR rats on 8.0% NaCl and the end of the 3rd week of therapy for DR and DS rats on 0.4% NaCl. These results suggest that enalapril may lower SBP by mechanisms other than those related to an action as a CEI.
在高盐(8.0%氯化钠)和正常盐(0.4%氯化钠)饮食条件下,对清醒的Dahl盐敏感(DS)和盐抵抗(DR)大鼠研究了马来酸依那普利(MK 421,一种新型血管紧张素转换酶抑制剂(CEI))和氢氯噻嗪(HTZ)对收缩压的影响。高盐饮食3周后,DS大鼠出现严重高血压,而DR大鼠的收缩压(SBP)正常。口服依那普利(15 - 100毫克×千克-1×天-1)和HTZ(60 - 400毫克×千克-1×天-1)可使高盐饮食的DS大鼠SBP显著降低(P < 0.001);然而,直到治疗4周后,剂量分别为30和150毫克×千克-1×天-1时才观察到这种情况。此外,单独使用依那普利治疗可显著降低所有组大鼠的SBP,无论饮食或Dahl品系如何(P < 0.001),但在8.0%氯化钠饮食的DR大鼠治疗7周结束时以及0.4%氯化钠饮食的DR和DS大鼠治疗3周结束时才观察到这种情况。这些结果表明依那普利可能通过与作为CEI的作用无关的机制降低SBP。