Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243250
Title: Regulation of intracellular calcium in isolated vascular smooth muscle cells
Author: Baro-Puigdemasa, Isabelle
ISNI:       0000 0001 3446 6026
Awarding Body: University of London
Current Institution: University College London (University of London)
Date of Award: 1993
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Abstract:
Vascular smooth muscle cells require a very precise regulation of intracellular calcium concentration, since this ion is responsible for the activation of smooth muscle contractile proteins and, subsequently, for the vascular tone. Experiments have been performed to investigate this regulation. A Ca 2+-sensitive fluorescent indicator: indo 1, has been used to measure changes of intracellular Ca2+ activity ([Ca2+]i) in enzymatically isolated smooth muscle cells of mesenteric secondary arteries from rat. Caffeine has been used to induce a Ca2+ release from the sarcoplasmic reticulum (SR) and to uncouple the SR and [Ca2+]i regulation. By means of Na+-free or La3+ -containing solutions, the relatively poor role of the Na-Ca exchange in the Ca2+ extrusion during caffeine application has been shown. Furthermore, because of its slow pumping rate, the sarcolemmal Ca 2+-ATPase contributes at a minor level to the [Ca2+]i decrease during Ca2+ load. Sarcolemmal mechanisms are responsible though for resting [Ca2+]i maintenance. Excitation-contraction coupling has been investigated. Ca2+-dependence and voltage-independence of SR Ca2+ release have been demonstrated by means of caffeine and high external K+ concentrations. Pharmacomechanical coupling of the α-adrenergic stimulation has been studied. Noradrenergic stimulation induced intracellular mobilization of Ca2+ and no contribution of extracellular Ca2+ entry to the [Ca2+]i increase could be detected. The effects of noradrenaline, caffeine and thapsigargin, allowed the description of the functional heterogeneity of the SR. Various results are in favour of the physical continuity between the IP3 sensitive and insensitive Ca2+ stores with only limited intraluminal exchanges. A model describing qualitatively and quantitatively SR refilling after Ca2+ loss is also proposed. Finally, it appears that the SR has a double function: (i) it acts as an amplifier of the external stimulations and (ii) it plays a key role in Ca2+ excess buffering.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.243250  DOI: Not available
Keywords: Sarcoplasmic reticulum
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