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Excess nicotinamide inhibits methylation-mediated
ORIGINAL ARTICLE
Excess nicotinamide inhibits methylation-mediated
degradation of catecholamines in normotensives
and hypertensives
Wu-Ping Sun1, Da Li1, Yong-Zhi Lun2, Xiao-Jie Gong2, Shen-Xia Sun2, Ming Guo3, Li-Xin Jing2,
Li-Bin Zhang4, Fu-Cheng Xiao1 and Shi-Sheng Zhou1,2
Nicotinamide and catecholamines are both degraded by S-adenosylmethionine-dependent methylation. Whether excess
nicotinamide affects the degradation of catecholamines is unknown. The aim of this study was to investigate the effect of
nicotinamide on the methylation status of the body and methylation-mediated catecholamine degradation in both normotensives
and hypertensives. The study was conducted in 19 normotensives and 27 hypertensives, using a nicotinamide-loading test
(100 mg orally). Plasma nicotinamide, N1-methylnicotinamide, homocysteine (Hcy), betaine, norepinephrine, epinephrine,
normetanephrine and metanephrine levels before and 5 h after nicotinamide loading were measured. Compared with
normotensives, hypertensives had higher baseline (fasting) levels of plasma nicotinamide, Hcy and norepinephrine, but lower
levels of plasma normetanephrine, a methylated norepinephrine derivative. Nicotinamide loading induced a significant increase
in the levels of plasma N1-methylnicotinamide and norepinephrine, and a significant decrease in the levels of O-methylated
epinephrine (metanephrine) and betaine, a major methyl donor, in both hypertensives and normotensives. Moreover,
nicotinamide-loading significantly increased plasma Hcy levels, but decreased plasma normetanephrine levels in normotensives.
The baseline levels of plasma epinephrine in hypertensives were similar to those of normotensives, but the post-nicotinamide-
loading levels of plasma epinephrine in hypertensives were higher than those of normotensives. This study demonstrated that
excess nicotinamide might deplete the labile methyl pool, increase Hcy generation and inhibit catecholamine degradation.
It also revealed that hypertensiv
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