Literature DB >> 8045836

Responses to pressure and vasoactive agents by isolated pulmonary arteries from monocrotaline-treated rats.

J A Madden1, P A Keller, R M Effros, C Seavitte, J S Choy, A D Hacker.   

Abstract

Intralobar and side branch pulmonary arteries removed from rats 7, 14, and 21 days after injection with monocrotaline (MCT) were cannulated and pressurized, and their responses to potassium chloride, norepinephrine, acetylcholine, and angiotensin II were measured. Static pressure-diameter curves were also performed, and arterial distensibility was calculated. Arteries from all three MCT-treated groups showed reduced responses to potassium chloride and angiotensin II compared with control arteries (P < 0.05). The norepinephrine response was significantly reduced in arteries from the 14- and 21-day groups (P < 0.05). Dilations in response to acetylcholine were similar in arteries from the control and 7-day groups but were reduced compared with those in control vessels from the 14- and 21-day groups (P < 0.05). Compared with control values, the slopes of the pressure-diameter curves and the arterial distensibility decreased significantly with time after MCT treatment (P < 0.05). Values for arterial distensibilities obtained in the isolated pulmonary arteries support the theory that structural changes that occur as a result of MCT administration contribute to vessel stiffness. The acetylcholine-induced dilation of vessels from MCT-treated rats indicates that endothelium-derived factors are still produced, but diminished vasodilation coupled with decreased distensibilities after MCT suggest that abnormal vascular remodeling rather than a change in agonist sensitivity may be responsible for the reduced responsiveness seen in these arteries.

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Year:  1994        PMID: 8045836     DOI: 10.1152/jappl.1994.76.4.1589

Source DB:  PubMed          Journal:  J Appl Physiol (1985)        ISSN: 0161-7567


  3 in total

1.  Rhythmical contractions in pulmonary arteries of monocrotaline-induced pulmonary hypertensive rats.

Authors:  Akihiko Kiyoshi; Tomohisa Ishikawa; Ken-ichi Hayashi; Yoshiyuki Iwatsuki; Kunio Ishii; Koichi Nakayama
Journal:  Pflugers Arch       Date:  2003-09-27       Impact factor: 3.657

2.  Perindopril, an angiotensin converting enzyme inhibitor, in pulmonary hypertensive rats: comparative effects on pulmonary vascular structure and function.

Authors:  T K Jeffery; J C Wanstall
Journal:  Br J Pharmacol       Date:  1999-12       Impact factor: 8.739

Review 3.  Pulmonary vascular stiffness: measurement, modeling, and implications in normal and hypertensive pulmonary circulations.

Authors:  Kendall S Hunter; Steven R Lammers; Robin Shandas
Journal:  Compr Physiol       Date:  2011-07       Impact factor: 9.090

  3 in total

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