β-Adrenergic-mediated vasodilation in young men and women: cyclooxygenase restrains nitric oxide synthase

Autor: Joshua J. Sebranek, Jacqueline K. Limberg, Marlowe W. Eldridge, William G. Schrage, J. Mikhail Kellawan, Garrett L. Peltonen, Rebecca E. Johansson, John W. Harrell
Rok vydání: 2016
Předmět:
Adult
Male
Agonist
medicine.medical_specialty
Mean arterial pressure
Physiology
medicine.drug_class
Prostaglandin
Vasodilation
030204 cardiovascular system & hematology
Microcirculation
03 medical and health sciences
chemistry.chemical_compound
Integrative Cardiovascular Physiology and Pathophysiology
Sex Factors
0302 clinical medicine
Physiology (medical)
Internal medicine
medicine
Humans
Infusions
Intra-Arterial

Cyclooxygenase Inhibitors
Enzyme Inhibitors
omega-N-Methylarginine
biology
business.industry
Isoproterenol
Ultrasonography
Doppler

Adrenergic beta-Agonists
Nitric oxide synthase
Forearm
Endocrinology
chemistry
Prostaglandin-Endoperoxide Synthases
biology.protein
Omega-N-Methylarginine
Female
Cyclooxygenase
Nitric Oxide Synthase
Cardiology and Cardiovascular Medicine
business
Ketorolac
030217 neurology & neurosurgery
Zdroj: American Journal of Physiology-Heart and Circulatory Physiology. 310:H756-H764
ISSN: 1522-1539
0363-6135
DOI: 10.1152/ajpheart.00886.2015
Popis: We tested the hypothesis that women exhibit greater vasodilator responses to β-adrenoceptor stimulation compared with men. We further hypothesized women exhibit a greater contribution of nitric oxide synthase and cyclooxygenase to β-adrenergic-mediated vasodilation compared with men. Forearm blood flow (Doppler ultrasound) was measured in young men ( n = 29, 26 ± 1 yr) and women ( n = 33, 25 ± 1 yr) during intra-arterial infusion of isoproterenol (β-adrenergic agonist). In subset of subjects, isoproterenol responses were examined before and after local inhibition of nitric oxide synthase [ NG-monomethyl-l-arginine (l-NMMA); 6 male/10 female] and/or cyclooxygenase (ketorolac; 5 male/5 female). Vascular conductance (blood flow ÷ mean arterial pressure) was calculated to assess vasodilation. Vascular conductance increased with isoproterenol infusion ( P < 0.01), and this effect was not different between men and women ( P = 0.41). l-NMMA infusion had no effect on isoproterenol-mediated dilation in men ( P > 0.99) or women ( P = 0.21). In contrast, ketorolac infusion markedly increased isoproterenol-mediated responses in both men ( P < 0.01) and women ( P = 0.04) and this rise was lost with subsequent l-NMMA infusion (men, P < 0.01; women, P < 0.05). β-Adrenergic vasodilation is not different between men and women and sex differences in the independent contribution of nitric oxide synthase and cyclooxygenase to β-mediated vasodilation are not present. However, these data are the first to demonstrate β-adrenoceptor activation of cyclooxygenase suppresses nitric oxide synthase signaling in human forearm microcirculation and may have important implications for neurovascular control in both health and disease.
Databáze: OpenAIRE