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Inhibition of cystathionine-gamma lyase dampens vasoconstriction in mouse and human intracerebral arterioles

Peleli, Maria (författare)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Science for Life Laboratory, SciLifeLab,Univ Southern Denmark, Inst Mol Med, Dept Cardiovasc & Renal Res, Odense, Denmark.;Natl & Kapodistrian Univ Athens, Dept Pharm, Lab Pharmacol, Athens, Greece.;Acad Athens, Clin Expt Surg & Translat Res Ctr, Biomed Res Fdn, Athens, Greece.
Lyngso, Kristina S. (författare)
Univ Southern Denmark, Inst Mol Med, Dept Cardiovasc & Renal Res, Odense, Denmark.
Poulsen, Frantz Rom (författare)
Odense Univ Hosp, Dept Neurosurg, Odense, Denmark.;Univ Southern Denmark, Dept Clin Res, Odense, Denmark.;BRIDGE Brain Res Interdisciplinary Guided Excellen, Odense, Denmark.;OPEN Odense Patient Data Explorat Network, Odense, Denmark.
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Hansen, Pernille B. L. (författare)
Univ Southern Denmark, Inst Mol Med, Dept Cardiovasc & Renal Res, Odense, Denmark.
Papapetropoulos, Andreas (författare)
Natl & Kapodistrian Univ Athens, Dept Pharm, Lab Pharmacol, Athens, Greece.;Acad Athens, Clin Expt Surg & Translat Res Ctr, Biomed Res Fdn, Athens, Greece.
Stubbe, Jane (författare)
Univ Southern Denmark, Inst Mol Med, Dept Cardiovasc & Renal Res, Odense, Denmark.;Univ Southern Denmark, Inst Mol Med, Dept Cardiovasc & Renal Res, JB Winslows Vej 21,3rd floor, DK-5000 Odense C, Denmark.
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 (creator_code:org_t)
John Wiley & Sons, 2023
2023
Engelska.
Ingår i: Acta Physiologica. - : John Wiley & Sons. - 1748-1708 .- 1748-1716. ; 239:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • AimIn extracerebral vascular beds cystathionine-gamma lyase (CSE) activity plays a vasodilatory role but the role of this hydrogen sulfide (H2S) producing enzyme in the intracerebral arterioles remain poorly understood. We hypothesized a similar function in the intracerebral arterioles. MethodsIntracerebral arterioles were isolated from wild type C57BL/6J mouse (9-12 months old) brains and from human brain biopsies. The function (contractility and secondary dilatation) of the intracerebral arterioles was tested ex vivo by pressure myography using a perfusion set-up. Reverse transcription polymerase chain reaction was used for detecting CSE expression. ResultsCSE is expressed in human and mouse intracerebral arterioles. CSE inhibition with L-propargylglycine (PAG) significantly dampened the K+-induced vasoconstriction in intracerebral arterioles of both species (% of maximum contraction: in human control: 45.4 & PLUSMN; 2.7 versus PAG: 27 & PLUSMN; 5.2 and in mouse control: 50 & PLUSMN; 1.5 versus PAG: 33 & PLUSMN; 5.2) but did not affect the secondary dilatation. This effect of PAG was significantly reversed by the H2S donor sodium hydrosulfide (NaSH) in human (PAG + NaSH: 38.8 & PLUSMN; 7.2) and mouse (PAG + NaSH: 41.7 & PLUSMN; 3.1) arterioles, respectively. The endothelial NO synthase (eNOS) inhibitor, N & omega;-Nitro-l-arginine methyl ester (L-NAME), and the inhibitor of soluble guanylate cyclase (sGC), 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ) reversed the effect of PAG on the K+-induced vasoconstriction in the mouse arterioles and attenuated the K+-induced secondary dilatation significantly. ConclusionCSE contributes to the K+-induced vasoconstriction via a mechanism involving H2S, eNOS, and sGC whereas the secondary dilatation is regulated by eNOS and sGC but not by CSE.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Nyckelord

contractility
cystathionine-gamma lyase
endothelial NO synthase
hydrogen sulfide
intracerebral arterioles
soluble guanylate cyclase

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