MOHAMMADI NAGHADEH M, McGRATH J. INFLUENCE OF ENDO THELIUM REMOVAL AND LNAME ON RESPONSES OF RAT COMMON CAROTID ARTERY TO α-ADRENOCEPTOR AGONISTS. Med J Islam Repub Iran 2000; 14 (1) :87-91
URL:
http://mjiri.iums.ac.ir/article-1-906-en.html
From the Department of Physiology, Faculty of Medicine. Tabriz University of Medical Sciences, Tabriz. I. R. Iran
Abstract: (4677 Views)
In this study we investigated the effects of endothelium removal and L-NAME
on responses to α-adrenoceptor agonists. Male Wistar rats were killed by overdose
with pentobarbitone sodium, after which the left and right common carotid arteries
were removed. Rings of arteries 3-4 mm in length were cut from each vessel and
then mounted in 10 mL isolated organ bath, bathed in Krebs maintained at 37°C
and gassed with 95% 02 plus 5% CO2, The preparations were allowed to
equilibrate for an hour. L-NAME was added approximately 10-15 min prior to the
onset of cumulative concentration-response curves (CCRC) to an agonist. In some
preparations the endothelial layer was removed mechanically by gently rolling the
tissue around a thin wire. Removal of the endothelium was confirmed
pharmacologically by a lack of relaxant response to the potent endotheliumdependent
vasodilator acetylcholine. Inhibition of NO synthesis by L-NAME
results in significant vasoconstriction. L-NAME prevented the relaxation of rat
carotid artery by acetylcholine, suggesting that both basal and stimulated release
of nitric oxide can regulate vascular tone in this artery. Mechanical disruption of
the vascular endothelium reduced, but did not abolish, the ability of L-NAME to
produce contraction. This suggests an extra-endothelial site for nitric oxide
synthesis in rat common carotid artery. Inhibition of nitric oxide synthase with LNAME
potentiated responses to phenylephrine and UK-14304 but not to
noradrenaline. Mechanical disruption of the vascular endothelium potentiated
responses to UK-14304, phenylephrine and noradrenaline. We suggest that
constitutive NO activity has substantial inhibitory influence on vasoconstrictor
responses to phenylephrine and UK-14304 but not to noradrenaline.