Altered microvascular responses to C5a in rat striated muscle during two-kidney, one clip renovascular hypertension

OBJECTIVETo determine how two-kidney, one clip (2-K,1 C) renovascular hypertension alters microvascular responses in rat striated muscle to complement C5a, one of the most important inflammatory mediators. METHODS2-K,1C hypertension was induced in male Sprague-Dawley rats. Under anesthesia with pent...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of hypertension 1995-02, Vol.13 (2), p.227-234
Hauptverfasser: Yang, Sai, Luo, Hong Y, Wilson, Mark A, Wead, William B, Harri, Patrick D
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:OBJECTIVETo determine how two-kidney, one clip (2-K,1 C) renovascular hypertension alters microvascular responses in rat striated muscle to complement C5a, one of the most important inflammatory mediators. METHODS2-K,1C hypertension was induced in male Sprague-Dawley rats. Under anesthesia with pentobarbital (50 mg/kg, intraperitoneally) the cremaster muscle microcirculatory preparation with intact neurovascular connections was studied in vivo by closed-circuit videomicroscopy. Recombinant human C5a was applied topically in the tissue bath at concentrations of 10 or 10 and 10mol/l, consecutively. Changes in the microvessel diameters in small arterioles, large arterioles and venules were measured. RESULTSIn normotensive rats complement C5a induces a significant dilation in small arterioles at low bath concentrations (10 or 10mol/l), but the dilation is attenuated at a higher concentration (10mol/1). In contrast, in 2-K,1C hypertensive rats C5a constricts small arterioles at a low concentration (10 or 10mol/1) but the dilates them at a higher concentration (10 mol/l). Large arterioles and venules have minimal responses to C5a in either normotensive or 2-K, 1C hypertensive rats. CONCLUSION2-K, 1C hypertension dramatically alters C5a-induced microvascular responses in small arterioles. The alteration might be attributable to the enhanced vasoconstrictor mechanisms and impaired vasodilator mechanisms during 2-K, 1C renovascular hypertension.
ISSN:0263-6352
1473-5598
DOI:10.1097/00004872-199502000-00010