E. Nisoli et al., EFFECTS OF NITRIC-OXIDE ON PROLIFERATION AND DIFFERENTIATION OF RAT BROWN ADIPOCYTES IN PRIMARY CULTURES, British Journal of Pharmacology, 125(4), 1998, pp. 888-894
1 In the present work, we study the effect of NO on the proliferation
and differentiation of brown fat cells in primary cultures. 2 Brown fa
t precursor cells isolated from rat brown adipose tissue were cultured
for 8 days until confluence and treated daily with the NO donating ag
ents, S-nitroso-acetyl penicillamine (SNAP) or S-nitroso-L-glutathione
(GSNO). Both agents (300 mu M) decreased cell proliferation approxima
tely 8 fold on day 8. The inhibitory effect of NO was unlikely to be d
ue to cytotoxicity since (i) cells never completely lost their prolife
ration capacity even after 8 days of exposure to repeated additions of
SNAP or GSNO, and (ii) the inhibitory effect was reversible after rem
oval of the media containing NO donors. 3 Daily treatment with nitric
oxide synthase inhibitors, such as NG-nitro-L-arginine methyl ester (L
-NAME, 300 mu M), led to the stimulation of cell proliferation by 44 /- 5%, n = 3, suggesting that NO, endogenously produced in brown adipo
cytes, may be involved in modulating cell growth. 4 Daily treatment wi
th both SNAP or GSNO induced significant mitochondriogenesis, measured
as the mitochondrial conversion of 3-[4,5-dimethylthiazol-2-yl-]-2,5-
diphenyl tetrazolium bromide (MTT) to formazan, whilst daily treatment
with L-NAME was without effect. 5 The inhibition of cell proliferatio
n by NO donors was accompanied by the expression of two genes coding f
or peroxisome proliferator activated receptor-gamma and uncoupling pro
tein-1, which are upregulated during differentiation. 6 Increasing cyc
lic GMP in cells by 8-bromo-cyclic GMP (100-1000 mu M) did not reprodu
ce the observed NO effects on either cell number or gene expression. O
n the other hand, chronic treatment with the inhibitor of the NO-stimu
lated guanylyl cyclase, 1H-[1,2,4]oxadiazole[4,3-a]quinoxalin-1-one (O
DQ), reduced the expression of peroxisome proliferator activated recep
tor-gamma and uncoupling protein-1.