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September 1, 1992Journal of Hypertension242 citations

Effect of local intra-arterial NG-monomethyl-L-arginine in patients with hypertension

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ACAlison CalverJCJoe CollierSMSalvador Moncada

Key Result

Local intra-arterial infusion of L-NMMA produced a significantly smaller reduction in forearm blood flow in untreated hypertensive patients compared to normotensive controls.

Key Points

  • The study aims to evaluate nitric oxide-mediated dilation in hypertensive patients compared to normotensive controls.
  • Examined forearm blood flow response to noradrenaline and NG-monomethyl-L-arginine in untreated hypertensive patients and normotensive controls.
  • Administered drugs locally into the brachial artery and measured forearm blood flow using venous occlusion plethysmography.
  • Included 7 untreated hypertensive patients and 17 normotensive controls.
  • In hypertensive patients, L-NMMA was significantly less effective than noradrenaline with increased threshold dose for vasoconstriction.
  • There was a significant negative correlation between L-NMMA response and blood pressure in hypertensives.
  • The response to L-NMMA was significantly lower in hypertensives compared to normotensives, while noradrenaline response showed no statistical difference between groups.

Study Design

Type

Case-Control (n=24)

Structured PICO

Does local intra-arterial NG-monomethyl-L-arginine alter forearm blood flow differently in untreated hypertensive patients compared to normotensive controls?

P
Population
24 participants, including 7 untreated hypertensive patients and 17 normotensive controls, assessed for forearm blood flow responses.
I
Intervention
Local intra-arterial infusion of NG-monomethyl-L-arginine (L-NMMA) (1, 2, and 4 μmol/min) into the brachial artery
C
Comparator
Noradrenaline infusion (60, 120, and 240 pmol/min) as an internal control, and a normotensive control group
O
Outcome
Forearm blood flow (FBF) response measured using venous occlusion plethysmographysurrogate

Untreated hypertensive patients exhibit impaired basal nitric oxide-mediated vasodilation in the forearm arteriolar bed compared to normotensive controls.

Abstract

Objective: There is indirect evidence that the nitric oxide system may be impaired in hypertensive patients. The objective of this study was to examine basal nitric oxide-mediated dilation in hypertensive patients. Design: The forearm blood flow (FBF) response to noradrenaline and NG-monomethyl-L-arginine (L-NMMA), a stereospecific inhibitor of nitric oxide synthesis, was compared in seven untreated hypertensive patients and 17 normotensive controls. Methods: Drugs were infused locally into the brachial artery and FBF measured using venous occlusion plethysmography. Results: In normotensives noradrenaline (60, 120 and 240 pmol/min) and L-NMMA (1,2 and 4 μmol/min) produced similar reductions in resting FBF. In the hypertensives L-NMMA was significantly less effective than noradrenaline, such that the threshold dose for L-NMMA vasoconstriction was increased and the overall response to L-NMMA reduced. Furthermore, when noradrenaline was used as an internal control there was a significant negative relationship between the response to L-NMMA and blood pressure. When the responses to L-NMMA and noradrenaline were compared between groups, the response to L-NMMA was significantly less in hypertensives compared with normotensives, whereas there was no statistical difference in the response to noradrenaline between the two groups. Conclusions: The results suggest an abnormality of basal nitric oxide-mediated dilation in the forearm arteriolar bed of patients with untreated essential hypertension.

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Cite This Study

Calver et al. (1992) conducted a case-control in Hypertension (n=24). NG-monomethyl-L-arginine (L-NMMA) vs. Normotensive controls was evaluated on Forearm blood flow (FBF) response. Local intra-arterial infusion of L-NMMA produced a significantly smaller reduction in forearm blood flow in untreated hypertensive patients compared to normotensive controls.

synapsesocial.com/papers/6a2187c94f27a676ef8b882ahttps://doi.org/10.1097/00004872-199209000-00017
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