POSSIBLE INVOLVEMENT OF L-ARGININE-NITRIC OXIDE PATHWAY IN MODULATINGREGIONAL BLOOD-FLOW TO BROWN ADIPOSE-TISSUE OF RATS
Citation
Y. Uchida et al., POSSIBLE INVOLVEMENT OF L-ARGININE-NITRIC OXIDE PATHWAY IN MODULATINGREGIONAL BLOOD-FLOW TO BROWN ADIPOSE-TISSUE OF RATS, Naunyn-Schmiedeberg's archives of pharmacology, 349(2), 1994, pp. 188-193
Categorie Soggetti
Pharmacology & Pharmacy
SICI code
0028-1298(1994)349:2<188:PIOLOP>2.0.ZU;2-G
Abstract
To evaluate whether the L-arginine-nitric oxide (NO) pathway is involv
ed in the regulation of regional blood flow to brown adipose tissue (B
AT), the effects of two specific NO synthase inhibitors, N-G-nitro-L-a
rginine methyl ester (L-NAME) and N-G-monomethyl-L-arginine (L-NMMA),
on the blood flow to interscapular brown adipose tissue (IBAT) were st
udied in urethane-anesthetized rats. Regional blood flow in IBAT was m
easured with laser-Doppler flowmetry. An intravenous injection of L-NA
ME and L-NMMA, but not of either D-enantiomer, caused a transient and
dose-dependent increase in IBAT blood flow Dose-response curves for th
ese NO synthase inhibitors showed that L-NAME was more potent than L-N
MMA in increasing IBAT blood flow. We also observed a concomitant pres
ser effect accompanied by a slight decrease in heart rate following in
travenous injection of L-NAME and L-NMMA. An elevation of IBAT blood f
low and blood pressure induced by both L-NAME and L-NMMA was reversed
by L-arginine in an enantiomerically specific manner. The increase in
IBAT blood flow induced by NO synthase inhibitors was of shorter durat
ion and less sensitive to L-arginine than the increase in blood pressu
re. Our results show that the IBAT blood flow is increased by inhibiti
on of NO synthase and that the response of IBAT vasculature to NO synt
hase inhibitors is different from that of the resistance vessels which
regulate blood pressure. The involvement of L-arginine-NO pathways in
modulating microcirculation in IBAT is suggested.