Pregled bibliografske jedinice broj: 107609
Endogenous vascular remodeling in ischemic skeletal muscle : a role for nitric oxide
Endogenous vascular remodeling in ischemic skeletal muscle : a role for nitric oxide // Journal of Applied Physiology, 94 (2003), 3; 935-940 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 107609 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Endogenous vascular remodeling in ischemic skeletal muscle : a role for nitric oxide
Autori
Buckwalter, John B. ; Curtis, Valerie C. ; Valić, Zoran ; Ruble, Stephen B. ; Clifford, Philip S.
Izvornik
Journal of Applied Physiology (8750-7587) 94
(2003), 3;
935-940
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
blood flow; angiogenesis; arteriogenesis; rabbits; exercise
Sažetak
To test the hypothesis that nitric oxide (NO) production is essential for endogenous vascular remodeling in ischemic skeletal muscle, 22 New Zealand White rabbits were chronically instrumented with transit-time flow probes on the common iliac arteries and underwent femoral ligation to produce unilateral hindlimb ischemia. Iliac blood flow and arterial pressure were recorded at rest and during a graded exercise test. An osmotic pump connected to a femoral arterial catheter continuously delivered N-nitro-l-arginine methyl ester (a NO synthase inhibitor) or a control solution (N-nitro-d-arginine methyl ester or phenylephrine) to the ischemic limb over a 2-wk period. At 1, 3, and 6 wk after femoral ligation, maximal treadmill exercise blood flow in the ischemic limb was reduced compared with baseline in each group. However, maximal exercise blood flow was significantly (P < 0.05) lower in the l-NAME-treated group than in controls for the duration of the study: 48 +/- 4 vs. 60 +/- 5 ml/min at 6 wk. Consistent with the reduction in maximal blood flow response, the duration of voluntary exercise was also substantially (P < 0.05) shorter in the l-NAME-treated group: 539 +/- 67 vs. 889 +/- 87 s. Resting blood flow was unaffected by femoral ligation in either group. The results of this study show that endogenous vascular remodeling, which partially alleviated the initial deficit in blood flow, was interrupted by NO synthase inhibition. Therefore, we conclude that NO is essential for endogenous collateral development and angiogenesis in ischemic skeletal muscle in the rabbit.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE