Ethanol and the vasculature

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Ethanol and the vasculature

Postby gibbledygook » Thu Oct 30, 2008 12:43 am

I'm afraid to note that in my experience and from research on pubmed, it seems very likely that over-indulgence with alcohol will negatively impact the vasculature by causing excessive endothelin 1 reactivity.
1: J Pharmacol Exp Ther. 2006 Aug;318(2):819-27. Epub 2006 May 1. Links
Ethanol consumption enhances endothelin-1-induced contraction in the isolated rat carotid.Tirapelli CR, Casolari DA, Montezano AC, Yogi A, Tostes RC, Legros E, D'Orléans-Juste P, Lanchote VL, Uyemura SA, de Oliveira AM.
Department of Pharmacology, Faculty of Medicine of Ribeirão Preto, University of Sao Paulo, Sao Paulo, Sao Paulo, Brazil.

We investigated the mechanisms involved in the enhancement of endothelin (ET)-1 vascular reactivity induced by ethanol consumption. Ethanol intake for 2, 6, and 10 weeks enhanced the ET-1-induced contractile response of endothelium-intact but not endothelium-denuded rat carotid rings independently of the treatment duration. Conversely, phenylephrine-induced contraction was not affected by ethanol intake. The contraction induced by IRL1620 [succinyl-(Glu(9),Ala(11,15))-ET-1-(8-21)], a selective ET(B) agonist, was increased after treatment with ethanol in endothelium-intact but not in endothelium-denuded carotid rings. Moreover, ET-1- and IRL1620-induced relaxation was reduced in endothelium-intact phenylephrine-precontracted rings from ethanol-treated rats. Acetylcholine-induced relaxation was not affected by ethanol treatment. N(G)-Nitro-l-arginine methyl ester, 1H-[1,2,4]-oxadiazolo[4,3-a]quinoxalin-1-one, indomethacin, and tetraethylammonium reduced the relaxation induced by IRL1620 in carotid glands from control but not ethanol-treated rats. The mRNA levels for ET(A) and ET(B) receptors were not altered by ethanol consumption. However, ethanol treatment reduced the protein expression of ET(B) receptors. Furthermore, immunohistochemical assays showed reduced immunostaining for endothelial ET(B) receptors after treatment with ethanol. We conclude that ethanol consumption enhances ET-1-induced contraction in the rat carotid and that this response is not different among the three periods of treatment used in this study. Finally, the potentiation of ET-1-induced vascular reactivity is probably caused by reduced expression of relaxing endothelial ET(B) receptors.

PMID: 16651399 [PubMed - indexed for MEDLINE]
link
I reckon that we should only drink VERY modest quantities since the effects of alcohol in the long run disturb the functioning of the endothelium.
3 years antibiotics, 06/09 bilateral jug stents at C1, 05/11 ballooning of both jug valves, 07/12 stenting of renal vein, azygos & jug valve ballooning,
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Postby DIM » Thu Oct 30, 2008 1:16 pm

Alcohol reduces glutathione production thus is only bad for your health not to mention MS.
I'd say the only permitted alcohol (at moderate quantities) should be the red wine!
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Postby gibbledygook » Fri Oct 31, 2008 12:46 am

Yes, I agree. Thankfully that's just about the only alcohol I like drinking. But, boy, do I like drinking it!!! I also think that mixing alcohol with ginkgo and salvia, from my experience, is a very very BAD idea. Damm and blast it all.
3 years antibiotics, 06/09 bilateral jug stents at C1, 05/11 ballooning of both jug valves, 07/12 stenting of renal vein, azygos & jug valve ballooning,
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