ArticleThe Journal of physiology1997
Effects of hypoxia on [Ca2+]i, pHi and myosin light chain phosphorylation in guinea-pig taenia caeci.
Article in The Journal of physiology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 32 citations in OpenAlex.
- Effects of 17beta-oestradiol on rat detrusor smooth muscle contractility.Experimental physiology · 2009Article
- Ca2+-desensitizing hypoxic vasorelaxation: pivotal role for the myosin binding subunit of myosin phosphatase (MYPT1) in porcine coronary artery.The Journal of physiology · 2006Article
- HSP20 phosphorylation and interstitial metabolites in hypoxia-induced dilation of swine coronary arteries.Acta physiologica Scandinavica · 2005Article
- Ca2+-independent hypoxic vasorelaxation in porcine coronary artery.The Journal of physiology · 2005Article
- Hypoxia inhibits contraction but not calcium channel currents or changes in intracellular calcium in arteriolar muscle cells.Microcirculation (New York, N.Y. : 1994) · 2003Article
- Smooth muscle and NMR review: an overview of smooth muscle metabolism.Molecular and cellular biochemistry · 2003Review
- Hypoxia and smooth muscle function: key regulatory events during metabolic stress.The Journal of physiology · 1998Review
Corrections and comments
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Authors and funding
4 authors at 1 institution in 2 countries.
Funding
Abstract
1. Hypoxia (achieved by bubbling with N2 instead of O2) reduces the force of a KCl (40 mM)-induced contracture to approximately 10% of the control value in guinea-pig taenia caeci. The underlying mechanism of this relaxation in response to hypoxia was investigated by measuring the major cell signalling parameters, intracellular Ca2+ concentration ([Ca2+]i) and myosin regulatory light chain (LC20) phosphorylation (MLC-P1), as well as intracellular pH (pHi), a factor often suggested to mediate hypoxic relaxation of muscle. 2. [Ca2+]i, measured using the ratiometric fluorescent dye fura-2, increased when 40 mM KCl was added to physiological saline solution (PSS) (peak value assigned 100%), and the steady state after 15 min was 92.8%. There were no detectable decreases in [Ca2+]i during hypoxia. 3. MLC-Pi, measured using isoelectric focusing-polyacrylamide gel electrophoresis and identified using Western blotting, increased from 9% of the total LC20 in Ca(2+)-free PSS to a peak value of 51% in 40 mM KCl-PSS. The steady-state value in hypoxia of 43% was not significantly different from that in control oxygenated conditions at the same point in time. 4. pHi, measured using the ratiometric fluorescent dye 2',7'-bis(carboxyethyl)-5(6)-carboxy-fluorescein (BCECF), under quiescent conditions (Ca(2+)-free PSS) was 7.23 and increased to 7.36 with 40 mM KCl. After imposition of hypoxia pHi remained unchanged despite the known increase in both lactate content and production. 5. As [Ca2+]i and MLC-Pi, key factors in activation, were not decreased by hypoxia and changes in pHi were minor, hypoxic relaxation in guinea-pig taenia caeci appears to be directly related to energy limitation rather than any oxygen-sensing mechanism.
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