ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2010
Sex-related decrease in [Ca2+]i signaling and Ca2+-dependent contraction in inferior vena cava of female rat.
Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 7 citations in OpenAlex.
- Gender differences in the regulation of MLCBiomedical reports · 2018Article
- Pregnancy-associated adaptations in [Ca2+]i-dependent and Ca2+ sensitization mechanisms of venous contraction: implications in pregnancy-related venous disorders.American journal of physiology. Heart and circulatory physiology · 2016Article
- Ryanodine receptors are uncoupled from contraction in rat vena cava.Cell calcium · 2013Article
- Varicose veins: role of mechanotransduction of venous hypertension.International journal of vascular medicine · 2012Article
- Estrogen receptor-mediated enhancement of venous relaxation in female rat: implications in sex-related differences in varicose veins.Journal of vascular surgery · 2010Article
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2 authors at 2 institutions in 1 country.
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Abstract
Sex differences in the incidence of varicose veins have been suggested; however, the venous mechanisms involved are unclear. We hypothesized sex-related differences in venous function and underlying distinctions in intracellular free calcium, [Ca(2+)](i), signaling and Ca(2+)-dependent mechanisms of venous contraction. Circular segments of inferior vena cava (IVC) from male and female Sprague-Dawley rats were suspended between two hooks, labeled with fura-2, and placed in a cuvet inside a spectrofluorometer for simultaneous measurement of isometric contraction and the 340/380 fluorescence ratio (indicative of [Ca(2+)](i)). In male IVC, phenylephrine (PHE; 10(-5) M) caused significant increase in contraction and [Ca(2+)](i). In female IVC, PHE-induced contraction was significantly reduced, but [Ca(2+)](i) did not differ significantly from males. Membrane depolarization by KCl (96 mM), which stimulates Ca(2+) influx, caused parallel increases in contraction and [Ca(2+)](i) in male IVC, and the KCl-induced contraction was significantly reduced in parallel with [Ca(2+)](i) in female IVC. In male IVC stimulated with 0 Ca(2+) KCl solution, the addition of increasing concentrations of extracellular Ca(2+) ([Ca(2+)](e)) (0.1, 0.3, 0.6, 1, and 2.5 mM) caused stepwise increases in contraction and [Ca(2+)](i), and both the KCl-induced [Ca(2+)](e)-contraction curve and the [Ca(2+)](e)-[Ca(2+)](i) curve were reduced in female IVC, suggesting reduced Ca(2+) entry via voltage-gated channels. The PHE-induced [Ca(2+)](e)-contraction curve was significantly reduced in females, but the [Ca(2+)](e)-[Ca(2+)](i) curve was similar in female and male IVC, suggesting the involvement of other mechanisms in addition to Ca(2+) entry. The [Ca(2+)](e)-contraction and [Ca(2+)](e)-[Ca(2+)](i) curves were used to construct the [Ca(2+)](i)-contraction relationship. The KCl-induced [Ca(2+)](i)-contraction relationship was superimposed in male and female IVC. In contrast, the PHE-induced [Ca(2+)](i)-contraction relationship was reduced and located to the right in female compared with male IVC, suggesting reduced [Ca(2+)](i) sensitivity of the venous contractile myofilaments. The reduced contraction, [Ca(2+)](i), and [Ca(2+)](i) sensitivity in female veins render them more prone to dilation. These sex-specific reductions in venous function, if they also occur in human veins, may play a role in the greater incidence of varicose veins in females.
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