Effects of monosodium glutamate-induced obesity in spontaneously hypertensive rats vs. Wistar Kyoto rats: Serum leptin and blood flow to brown adipose tissue
M. Iwase et al., Effects of monosodium glutamate-induced obesity in spontaneously hypertensive rats vs. Wistar Kyoto rats: Serum leptin and blood flow to brown adipose tissue, HYPERTENS R, 23(5), 2000, pp. 503-510
We compared the effects of hypothalamic obesity induced by neonatal monosod
ium glutamate (MSG) treatment between spontaneously hypertensive rats(SHR)
and normotensive Wistar Kyoto rats (WKY). Newborn WKY and SHR were injected
intraperitoneally with 4 mg/kg body weight of MSG daily for 5 days. At 6 m
onths of age, the obesity of SHR was more advanced than that of WKY, but at
14 months of age the severity of obesity was similar between the two strai
ns, Hypertriglyceridemia was enhanced in MSG-treated SHR as compared with M
SG-treated WKY, Systolic blood pressure measured by the tail-cuff method wa
s consistently lower in MSG-treated SHR than in control SHR, whereas blood
pressure was not affected by neonatal MSG treatment in WKY. Food restrictio
n reduced body weight more in control SHR than in control WKY, with the for
mer also showing enhanced ketogenesis, Neonatal MSG treatment abolished the
accelerated reduction of body weight in SHR. Serum leptin concentration wa
s markedly increased in MSG-treated obese rats, though no differences were
seen between WKY and SHR in the control or MSG-treated groups. Serum leptin
was closely correlated with both Lee obese index and mesenteric fat weight
over the strain. Blood flow in interscapular brown adipose tissue (BAT) me
asured by Laser Doppler flowmetry was significantly increased in response t
o beta(3)-adrenoceptor agonist BRL26830A in both the control and MSG-treate
d rats. However, the response of blood flow was not affected by MSG treatme
nt or strain difference. The present study demonstrated some strain differe
nces in response to neonatal MSG treatment between WKY and SHR. These diffe
rences could not be explained by the difference in serum leptin level or be
ta(3)-adrenergic reactivity in BAT.