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一种新型二氢苯并呋喃类似物和依那普利对缺钠正常血压大鼠血压、血浆及组织血管紧张素转换酶活性的急性和慢性影响

Acute and chronic effects of a novel dihydrobenzofuran analogue and enalapril on blood pressure and plasma and tissue angiotensin converting enzyme activity in the sodium deficient normotensive rat.

作者信息

Longman S D, Howlett D R

机构信息

Beecham Pharmaceuticals Research Division, Harlow, Essex, UK.

出版信息

Arzneimittelforschung. 1988 May;38(5):678-82.

PMID:2843192
Abstract
  1. Changes occurring in plasma and tissue angiotensin converting enzyme (ACE) activity have been examined in relation to blood pressure response following acute and chronic administration of N-[N-[[4-(2,3-dihydro-2-benzofuranyl)-1- (ethoxycarbonyl)]-butyl]-(s)-alanyl]-(s)-proline (BRL 36378) and enalapril in the sodium deficient normotensive rat. 2. Both BRL 36378 and enalapril produced a reduction in blood pressure which was evident at 2 and 24 h after acute administration, or at 24 h after chronic (21 days) administration. This was accompanied by inhibition of ACE activity in both plasma and tissues. 3. The magnitude of ACE inhibition was greater following enalapril administration than achieved after BRL 36378 treatment; this was reflected by the greater fall in blood pressure evoked by enalapril. 4. Removal of the respective ACE inhibitors revealed an apparent increase in total enzyme in the plasma of animals dosed chronically with BRL 36378 and enalapril. The onset of this increase in total enzyme was rapid, as it was apparent in plasma at 24 h after a single oral dose of BRL 36378 and enalapril. 5. The increase in total enzyme in plasma may be related to the degree of ACE inhibition, since the increase in total enzyme was of greater magnitude after 21 days treatment with enalapril than following corresponding dosing with BRL 36378. 6. No consistent effects on total enzyme were observed in tissues following acute and chronic administration with the ACE inhibitors. 7. Stimulation of drinking behaviour was observed throughout the periods of chronic (7 and 21 days) administration with both BRL 36378 and enalapril.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 研究了在缺钠正常血压大鼠中,急性和慢性给予N-[N-[[4-(2,3-二氢-2-苯并呋喃基)-1-(乙氧羰基)]-丁基]-(S)-丙氨酰]-(S)-脯氨酸(BRL 36378)和依那普利后,血浆和组织中血管紧张素转换酶(ACE)活性的变化与血压反应的关系。2. BRL 36378和依那普利均可使血压降低,急性给药后2小时和24小时或慢性(21天)给药后24小时血压降低明显。同时,血浆和组织中的ACE活性均受到抑制。3. 依那普利给药后ACE抑制程度大于BRL 36378治疗后;依那普利引起的血压下降幅度更大即反映了这一点。4. 去除相应的ACE抑制剂后,长期给予BRL 36378和依那普利的动物血浆中总酶明显增加。这种总酶增加的起始迅速,单次口服BRL 36378和依那普利后24小时血浆中即可明显看出。5. 血浆中总酶的增加可能与ACE抑制程度有关,因为依那普利治疗21天后总酶增加幅度大于相应剂量的BRL 36378给药后。6. 急性和慢性给予ACE抑制剂后,组织中未观察到对总酶的一致影响。7. 在长期(7天和21天)给予BRL 36378和依那普利的整个期间均观察到饮水行为受到刺激。(摘要截选至250字)

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