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. 2014 Mar;102(3):211-8.
doi: 10.5935/abc.20140015. Epub 2014 Feb 10.

Stress alone or associated with ethanol induces prostanoid release in rat aorta via alpha2-Adrenoceptor

[Article in English, Portuguese]
Affiliations

Stress alone or associated with ethanol induces prostanoid release in rat aorta via alpha2-Adrenoceptor

[Article in English, Portuguese]
Rafaela de Fátima Ferreira Baptista et al. Arq Bras Cardiol. 2014 Mar.

Abstract

Background: Stress and ethanol are both, independently, important cardiovascular risk factors.

Objective: To evaluate the cardiovascular risk of ethanol consumption and stress exposure, isolated and in association, in male adult rats.

Methods: Rats were separated into 4 groups: Control, ethanol (20% in drinking water for 6 weeks), stress (immobilization 1h day/5 days a week for 6 weeks) and stress/ethanol. Concentration-responses curves to noradrenaline - in the absence and presence of yohimbine, L-NAME or indomethacin - or to phenylephrine were determined in thoracic aortas with and without endothelium. EC50 and maximum response (n=8-12) were compared using two-way ANOVA/Bonferroni method.

Results: Either stress or stress in association with ethanol consumption increased the noradrenaline maximum responses in intact aortas. This hyper-reactivity was eliminated by endothelium removal or by the presence of either indomethacin or yohimbine, but was not altered by the presence of L-NAME. Meanwhile, ethanol consumption did not alter the reactivity to noradrenaline. The phenylephrine responses in aortas both with and without endothelium also remained unaffected regardless of protocol.

Conclusion: Chronic stress increased rat aortic responses to noradrenaline. This effect is dependent upon the vascular endothelium and involves the release of vasoconstrictor prostanoids via stimulation of endothelial alpha-2 adrenoceptors. Moreover, chronic ethanol consumption appeared to neither influence noradrenaline responses in rat thoracic aorta, nor did it modify the increase of such responses observed as a consequence of stress exposure.

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Conflict of interest statement

Potential Conflict of Interest

No potential conflict of interest relevant to this article was reported.

Figures

Figure 1
Figure 1
Concentration-response curves to noradrenaline obtained from intact thoracic aorta rings taken from animals exposed to ethanol consumption and/or stress, in the absence or presence of L-NAME (10-4 M), indomethacin (10-5 M) or yohimbine (10-6 M). Values are expressed as means ± SEM. The number of independent determinations was 8-10. *Indicates a significant difference (p < 0.05) in relation to the control animals.
Figure 2
Figure 2
Concentration-response curves to noradrenaline obtained from denuded thoracic aorta rings taken from animals exposed to ethanol consumption and/or stress, in the absence or presence of L-NAME (10-4 M), indomethacin (10-5 M) or yohimbine (10-6 M). Values are expressed as means ± SEM. The number of independent determinations was 8-10.
Figure 3
Figure 3
Concentration-response curves to phenylephrine obtained from rings of thoracic aorta with and without endothelium taken from animals exposed to ethanol consumption and/or stress. Values are expressed as means ± SEM. The number of independent determinations was 8-10.
Figure 4
Figure 4
Plasma concentration of nitrite/nitrate determined by the Griess Reaction taken from animals exposed to ethanol consumption and/or stress. Values are expressed as means ± SEM. The number of independent determinations was 10-12.

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