2006
DOI: 10.1016/j.lfs.2006.07.009
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Nitric oxide modulation of norepinephrine production in acupuncture points

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Cited by 27 publications
(12 citation statements)
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References 33 publications
(52 reference statements)
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“…L‐arginine‐derived NO synthesis modifies noradrenergic function, which contributes to low resistance characteristics of acupoints [4]. Consistently, enhanced 3H‐NE synthesis/release in acupoints/meridians is facilitated by the presence of an exogenous NO donor and inhibited by an inhibitor of NO synthesis [5]. Recent studies have demonstrated that EA stimulation of ST 36 increases the production of NO in arterioles [22].…”
Section: Discussionmentioning
confidence: 87%
“…L‐arginine‐derived NO synthesis modifies noradrenergic function, which contributes to low resistance characteristics of acupoints [4]. Consistently, enhanced 3H‐NE synthesis/release in acupoints/meridians is facilitated by the presence of an exogenous NO donor and inhibited by an inhibitor of NO synthesis [5]. Recent studies have demonstrated that EA stimulation of ST 36 increases the production of NO in arterioles [22].…”
Section: Discussionmentioning
confidence: 87%
“…EA stimulation induces a significant release of NO following dermal microdialysis in the acupoint but not in the NMCR in humans [35]. L-arginine-derived NO synthesis increases low resistance characteristics of acupoints [37], and norepinephrine turnover rate in acupoints/meridians is facilitated by presence of NO [38]. Consistently, cutaneous vasodilation induced by acupuncture stimulation in the forearms of humans is attenuated by application of NO synthesis inhibitor, which suggest that L-arginine-derived NO synthesis contributes to cutaneous vasodilation induced by acupuncture stimulation [39].…”
Section: Discussionmentioning
confidence: 99%
“…Hypertension is an important presenting feature of renal disease and is probably one of the most important factors contributing to the progression of CKD [6,31,32] . Recent studies have demonstrated that EA on the stomach at the 36th point (ST-36) induces upregulation of neuronal nitric oxide synthase (NOS) expression in the gracile nucleus and medial nucleus tractus solitarius, and this can modify central cardiovascular regulation [33,34] . Kim et al [35] demonstrated that EA on ST-36 reduces blood pressure by modulation of endothelial NOS and neuronal NOS expression.…”
mentioning
confidence: 99%