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Effects of Spaceflight and Ground Recovery on Mesenteric Artery and Vein Constrictor Properties in Mice

Overview
Journal FASEB J
Specialties Biology
Physiology
Date 2012 Oct 27
PMID 23099650
Citations 18
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Abstract

Following exposure to microgravity, there is a reduced ability of astronauts to augment peripheral vascular resistance, often resulting in orthostatic hypotension. The purpose of this study was to test the hypothesis that mesenteric arteries and veins will exhibit diminished vasoconstrictor responses after spaceflight. Mesenteric arteries and veins from female mice flown on the Space Transportation System (STS)-131 (n=11), STS-133 (n=6), and STS-135 (n=3) shuttle missions and respective ground-based control mice (n=30) were isolated for in vitro experimentation. Vasoconstrictor responses were evoked in arteries via norepinephrine (NE), potassium chloride (KCl), and caffeine, and in veins through NE across a range of intraluminal pressures (2-12 cmH(2)O). Vasoconstriction to NE was also determined in mesenteric arteries at 1, 5, and 7 d postlanding. In arteries, maximal constriction to NE, KCl, and caffeine were reduced immediately following spaceflight and 1 d postflight. Spaceflight also reduced arterial ryanodine receptor-3 mRNA levels. In mesenteric veins, there was diminished constriction to NE after flight. The results indicate that the impaired vasoconstriction following spaceflight occurs through the ryanodine receptor-mediated intracellular Ca(2+) release mechanism. Such vascular changes in astronauts could compromise the maintenance of arterial pressure during orthostatic stress.

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References
1.
Hatton D, Yue Q, Chapman J, Xue H, Dierickx J, Roullet C . Blood pressure and mesenteric resistance arterial function after spaceflight. J Appl Physiol (1985). 2001; 92(1):13-7. DOI: 10.1152/jappl.2002.92.1.13. View

2.
McCurdy M, Colleran P, Muller-Delp J, Delp M . Effects of fiber composition and hindlimb unloading on the vasodilator properties of skeletal muscle arterioles. J Appl Physiol (1985). 2000; 89(1):398-405. DOI: 10.1152/jappl.2000.89.1.398. View

3.
Bullard R . Physiological problems of space travel. Annu Rev Physiol. 1972; 34:205-34. DOI: 10.1146/annurev.ph.34.030172.001225. View

4.
Behnke B, Kindig C, Musch T, Koga S, Poole D . Dynamics of microvascular oxygen pressure across the rest-exercise transition in rat skeletal muscle. Respir Physiol. 2001; 126(1):53-63. DOI: 10.1016/s0034-5687(01)00195-5. View

5.
Sayet I, Neuilly G, Mironneau J, Mironneau C . Influence of spaceflight, hindlimb suspension, and venous occlusion on alpha 1-adrenoceptors in rat vena cava. J Appl Physiol (1985). 1995; 78(5):1882-8. DOI: 10.1152/jappl.1995.78.5.1882. View