SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Mills Nicholas L.)
 

Sökning: WFRF:(Mills Nicholas L.) > Altered nitric oxid...

Altered nitric oxide bioavailability contributes to diesel exhaust inhalation-induced cardiovascular dysfunction in man

Langrish, Jeremy P (författare)
Unosson, Jon (författare)
Umeå universitet,Lungmedicin
Bosson, Jenny (författare)
Umeå universitet,Lungmedicin
visa fler...
Barath, Stefan (författare)
Umeå universitet,Lungmedicin
Muala, Ala (författare)
Umeå universitet,Lungmedicin
Blackwell, Scott (författare)
Söderberg, Stefan (författare)
Umeå universitet,Kardiologi
Pourazar, Jamshid (författare)
Umeå universitet,Lungmedicin
Megson, Ian L (författare)
Treweeke, Andrew (författare)
Sandström, Thomas (författare)
Umeå universitet,Lungmedicin
Newby, David E (författare)
Blomberg, Anders (författare)
Umeå universitet,Lungmedicin
Mills, Nicholas L (författare)
visa färre...
 (creator_code:org_t)
American stroke association, 2013
2013
Engelska.
Ingår i: Journal of the American Heart Association. - : American stroke association. - 2047-9980. ; 2:1, s. e004309-
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background Diesel exhaust inhalation causes cardiovascular dysfunction including impaired vascular reactivity, increased blood pressure, and arterial stiffness. We investigated the role of nitric oxide (NO) bioavailability in mediating these effects.Methods and Results In 2 randomized double-blind crossover studies, healthy nonsmokers were exposed to diesel exhaust or filtered air. Study 1: Bilateral forearm blood flow was measured during intrabrachial infusions of acetylcholine (ACh; 5 to 20 mu g/min) and sodium nitroprusside (SNP; 2 to 8 mu g/min) in the presence of the NO clamp (NO synthase inhibitor N-G-monomethyl-L-arginine (L-NMMA) 8 mu g/min coinfused with the NO donor SNP at 90 to 540 ng/min to restore basal blood flow). Study 2: Blood pressure, arterial stiffness, and cardiac output were measured during systemic NO synthase inhibition with intravenous L-NMMA (3 mg/kg). Following diesel exhaust inhalation, plasma nitrite concentrations were increased (68 +/- 48 versus 41 +/- 32 nmol/L; P=0.006) despite similar L-NMMA-induced reductions in basal blood flow (-20.6 +/- 14.7% versus -21.1 +/- 14.6%; P=0.559) compared to air. In the presence of the NO clamp, ACh and SNP caused dose-dependent vasodilatation that was not affected by diesel exhaust inhalation (P>0.05 for both). Following exposure to diesel exhaust, L-NMMA caused a greater increase in blood pressure (P=0.048) and central arterial stiffness (P=0.007), but reductions in cardiac output and increases in systemic vascular resistance (P>0.05 for both) were similar to those seen with filtered air.Conclusions Diesel exhaust inhalation disturbs normal vascular homeostasis with enhanced NO generation unable to compensate for excess consumption. We suggest the adverse cardiovascular effects of air pollution are, in part, mediated through reduced NO bioavailability.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

air pollution
endothelial function
nitric oxide
nitric oxide synthase
vascular biology

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy