Evidence that nitric oxide (NO) is involved in cytokine-mediated islet
beta-cell dysfunction and destruction in vitro has led to the hypothe
sis that increased production of NO may contribute to the pathogenesis
of insulin-dependent diabetes mellitus (IDDM), This study demonstrate
s that oral administration of N-omega-nitro-L-arginine methyl ester (a
n inhibitor of NO synthase) from 30 to 150 days of age significantly r
educed (P < 0.05) the incidence of IDDM in diabetes-prone BB/E rats. T
his supports the idea that NO plays a significant role in the pathogen
esis of IDDM in this animal model.