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September 1, 1987Circulation Research50 citationsOpen Access

Dual effects of norepinephrine and mechanisms of baroreceptor stimulation.

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PMP. A. MunchPTPeter ThorénABA M Brown

Key Result

Norepinephrine exhibited dual dose-dependent effects on arterial baroreceptors in rats, causing inhibition at low concentrations via smooth muscle contraction and excitation at high concentrations.

Structured PICO

What is the mechanism of action of norepinephrine on arterial baroreceptor discharge in an in vitro rat aortic arch preparation?

P
Population
In vitro aortic arch/aortic nerve preparation from rats used to study the mechanism of action of norepinephrine on arterial baroreceptors.
I
Intervention
Norepinephrine (NE) at varying concentrations (10(-10)-10(-5) M)
C
Comparator
Angiotensin II, sodium nitroprusside, prazosin, and baseline conditions
O
Outcome
Baroreceptor single-fiber dischargesurrogate

Norepinephrine modulates arterial baroreceptors through two distinct mechanisms: indirect inhibition via smooth muscle contraction at low doses and direct nerve excitation at high doses.

Abstract

The aim of this study was to determine the mechanism of action of norepinephrine (NE) on arterial baroreceptors (BRs), with the focus on regularly discharging, presumably myelinated fibers. With the use of an in vitro aortic arch/aortic nerve preparation from rats, BR single-fiber discharge was recorded simultaneously with aortic pressure and diameter. At constant suprathreshold pressure, NE had two dose-dependent effects. Inhibition was produced at low concentrations (10(-10)-10(-7) M), whereas excitation was produced at high concentrations (10(-6)-10(-5) M). Inhibition was attributed to BR unloading since the response was consistent with the fall in diameter, was mimicked by angiotensin II (10(-10)-10(-6) M), and was prevented by pretreatment with the smooth muscle relaxant sodium nitroprusside (10(-6) M) or the selective alpha 1-adrenergic antagonist, prazosin (10(-6) M). Excitation was attributed to direct activation of the BR endings since this response was independent of changes in diameter, was not mimicked by angiotensin II, and was not prevented by sodium nitroprusside but was blocked by prazosin. These results indicate that NE has two modes of action, one mediated by contraction of local vascular smooth muscle and the other due to direct excitation of the nerve endings. It was also found that BR discharge at given diameters decreased more when pressure was lowered (smooth muscle passive) than when the aorta constricted (smooth muscle active). Furthermore, if diameter was held constant during smooth muscle contraction, discharge increased, as opposed to decreasing at constant pressure. These later results suggest that BR responses to vasoactive agents reflect not only changes in wall dimension but perhaps changes in wall tension and/or the coupling relation between BR and smooth muscle structures.

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Cite This Study

Munch et al. (1987) studied this question. Norepinephrine was evaluated on Baroreceptor single-fiber discharge. Norepinephrine exhibited dual dose-dependent effects on arterial baroreceptors in rats, causing inhibition at low concentrations via smooth muscle contraction and excitation at high concentrations.

synapsesocial.com/papers/6a219d29153b2036cbf1e5f9https://doi.org/10.1161/01.res.61.3.409
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