Literature DB >> 198216

Central cardiovascular effects of SQ 14,225, an angiotensin-converting enzyme inhibitor in chloralose-anesthetized cats.

R R Vollmer, J A Boccagno.   

Abstract

Experiments were conducted in chloralose-anesthetized cats to investigate the central and peripheral cardiovascular effects of a new orally active angiotensin-converting inhibitor, SQ 14,225 (3-mercapto-2-D-methylpropanoyl-L-proline). I.v. administration of SQ 14,225 (0.31-3100 microgram/kg) antagonized the pressor responses to angiotensin I (AI) (310 ng/kg) i.v. in a dose-related manner but did not alter responses to angiotensin II (AII) (200 ng/kg) i.v. Similarly, intracerebroventricularly (i.c.v.) administered SQ 14,225 (0.31-310 microgram/kg perfused over 10 min) produced dose-related decreases in the centrally mediated pressor responses and heart increases elicited by AI (310 ng/kg) i.c.v. The central responses to AII (200 ng/kg) i.c.v. were not affected by SQ 14,225. Passage of SQ 14,225 out of the ventricular system into the systemic circulation was detected, but only at doses greater than that required to antagonize central AI responses. Doses of SQ 14,225 (310 microgram/kg and 3.1 mg/kg) i.v. which maximally inhibited i.v. AI responses, had no effect upon central AI activity. This finding suggests that passage of SQ 14,225 across the blood brain barrier into the central nervous system is restricted. Peripheral or central administration of SQ 14,225 produced only minimal transient decreases in blood pressure (less than 10 mm Hg). The results of these studies indicate that SQ 14,225 is a potent inhibitor of AI conversion in the brain as well as in the peripheral circulation.

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Year:  1977        PMID: 198216     DOI: 10.1016/0014-2999(77)90081-4

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  8 in total

1.  Continuous measurement of renal cortical blood flow and renal arterial blood flow during stimulation of the renal nerve.

Authors:  F A Spelman; P A Oberg
Journal:  Med Biol Eng Comput       Date:  1991-03       Impact factor: 2.602

Review 2.  Preclinical studies on angiotensin converting enzyme inhibitors.

Authors:  I L Natoff
Journal:  Cardiovasc Drugs Ther       Date:  1987       Impact factor: 3.727

3.  Orally active angiotensin-converting enzyme inhibitor (SO 14,225) as a treatment for essential hypertension.

Authors:  H R Brunner; H Gavras; B Waeber; G A Turini; D N McKinstry; R A Vukovich; I Gavras
Journal:  Br J Clin Pharmacol       Date:  1979       Impact factor: 4.335

4.  Blockade of pressor responses to angiotensins I and II and noradrenaline using phentolamine, propranolol and hexamethonium in conscious rabbits.

Authors:  B P Rowe; A R Noble; K A Munday
Journal:  Pflugers Arch       Date:  1979-11       Impact factor: 3.657

Review 5.  Captopril: a preliminary review of its pharmacological properties and therapeutic efficacy.

Authors:  R C Heel; R N Brogden; T M Speight; G S Avery
Journal:  Drugs       Date:  1980-12       Impact factor: 9.546

6.  Enalapril maleate versus captopril. A comparison of the hormonal and antihypertensive effects.

Authors:  C R Ayers; K M Baker; B A Weaver; M R Lehman
Journal:  Drugs       Date:  1985       Impact factor: 9.546

7.  Influence of various antihypertensive agents on lifespan of renal hypertensive rats.

Authors:  Z P Horovitz; M J Antonaccio; B Rubin; R E Panasevich
Journal:  Br J Clin Pharmacol       Date:  1979       Impact factor: 4.335

8.  Captopril-induced changes in prostaglandin production: relationship to vascular responses in normal man.

Authors:  S L Swartz; G H Williams; N K Hollenberg; L Levine; R G Dluhy; T J Moore
Journal:  J Clin Invest       Date:  1980-06       Impact factor: 14.808

  8 in total

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