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Polymorphisms in the renin-angiotensin system and endothelium-dependent vasodilation in normotensive subjects

Kurland, Lisa, 1960- (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Akut- och internmedicin,Department of Medical Sciences, Uppsala University Hospital, Sweden; Department of Medicine, University Hospital, Uppsala, Sweden
Melhus, Håkan (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Clinical pharmacogenetics and osteoporosis,Department of Medical Sciences, Uppsala University Hospital, Sweden
Sarabi, Mahziar (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Akut- och internmedicin,Department of Medical Sciences, Uppsala University Hospital, Sweden
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Millgård, Jonas (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Akut- och internmedicin,Department of Medical Sciences, Uppsala University Hospital, Sweden
Ljunghall, Sverker (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Department of Medical Sciences, Uppsala University Hospital, Sweden
Lind, Lars (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Akut- och internmedicin,Department of Medical Sciences, Uppsala University Hospital, Sweden
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 (creator_code:org_t)
2008-06-28
2001
English.
In: Clinical Physiology. - : Wiley. - 0144-5979 .- 1365-2281. ; 21:3, s. 343-349
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Our aim was to test the hypothesis that genes encoding components in the renin-angiotensin system influence endothelial vasodilatory function. METHODS: In 59 apparently healthy, normotensive individuals, endothelium-dependent vasodilation (EDV) and endothelial-independent vasodilation (EIDV) was evaluated by infusing metacholine and sodium nitroprusside into the brachial artery. Forearm blood flow was measured by venous occlusion plethysmography. The ACE insertion (I)/deletion (D) polymorphism, the T174M and M235T angiotensinogen restriction fragments length polymorphisms, the angiotensin II receptor type 1 (AT1R) A1166C, and the aldosterone synthase gene (CYP11B2) C-344T polymorphisms were analysed. RESULTS: When analysing the ACE, the two angiotensinogen and the aldosterone synthase CYP11B2 genotypes independently, no significant association with endothelial vasodilatory function was found. However, a significant reduction in endothelium-dependent vasodilation was observed in the subjects (n=9) with the ACE D allele and the angiotensinogen T174M genotype (P<0.05). Subjects with the AT1R genotype AC showed a reduction in both EDV (P=0.05) and EIDV (P=0.04) when compared with those with the AA genotype. CONCLUSIONS: The subjects with the ACE D allele in combination with the angiotensinogen T174M genotype are associated with a reduced EDV. This together with the observation that the AC AT1R genotype is associated with a reduction in both EDV and EIDV, supports the hypothesis that endothelial vasodilatory function is influenced by genes in the renin-angiotensinogen system.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Fysiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Physiology (hsv//eng)

Keyword

Adult
Aged
Aldosterone Synthase/genetics
Endothelium
Vascular/*physiology
Female
Gene Deletion
Humans
Male
Middle Aged
Nitroprusside/administration & dosage/pharmacology
Peptidyl-Dipeptidase A/*genetics
Polymorphism; Genetic
Polymorphism
Restriction Fragment Length
Receptor
Angiotensin
Type 1; Receptor; Angiotensin; Type 2
Receptors; Angiotensin/genetics
Renin-Angiotensin System/*genetics
MEDICINE
MEDICIN

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