1972
DOI: 10.1007/bf00589130
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Selective suppression of some components of spontaneous activity in various types of smooth muscle by iproveratril (verapamil)

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Cited by 150 publications
(66 citation statements)
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“…In some preparations, mechanical activity was strongly inhibited by cromakalim even when the slow wave amplitude was not reduced or even increased. In gastric antral muscle, the spikelike component at the top of the slow wave is considered the main determinant of the magnitude of the phasic contraction (Golenhofen & Lammel, 1972). Verapamil inhibits the spikelike component with little effect on slow waves and suppresses mechanical activity.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…In some preparations, mechanical activity was strongly inhibited by cromakalim even when the slow wave amplitude was not reduced or even increased. In gastric antral muscle, the spikelike component at the top of the slow wave is considered the main determinant of the magnitude of the phasic contraction (Golenhofen & Lammel, 1972). Verapamil inhibits the spikelike component with little effect on slow waves and suppresses mechanical activity.…”
Section: Discussionmentioning
confidence: 99%
“…Spontaneous electrical activity, which takes the form of slow waves in the antrum region of the guinea-pig stomach, is known to be relatively insensitive to Ca2" channel blockers, such as verapamil (Golenhofen & Lammel, 1972). The frequency and amplitude of the slow wave are also only very weakly voltage-dependent, when studied by the sucrosegap method (Tomita, 1981).…”
Section: Introductionmentioning
confidence: 99%
“…Thus, the trigger Ca for Ca release from the intracellular stores can be considered to enter via some Ca binding sites which are sensitive to La (KAWAMURA and YABU, 1978) and much more resistant to verapamil, because K-induced contracture was little inhibited by 10 ,uM verapamil ( Fig. 3B) which is also known as a Ca blocker (GOLENHOFEN and LAMMEL, 1972). It may be also argued that ACh-sensitive Ca store was depleted even after immersion in Ca-free high-K solution (without EGTA) in which no contracture was observed.…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, a new class of Ca 2+ -activated Cl -channel, anoctamin 1 (ANO1)/Tmem16a has been recently identified (Caputo et al, 2008;Yang et al, 2008). The spontaneous activity is not inhibited by a number of 1,4-dihydropyridine Ca 2+ channel antagonists, such as verapamil (Golenhofen et al, 1972), diltiazem (Ishikawa et al, 1985) and nifedipine (Liu et al, 1995;Dickens et al, 1999;Ishikawa et al, 2004). Therefore, unlike smooth muscle cells, ICC-MY pacemaking does not employ L-type Ca 2+ channels as the major Ca 2+ signaling pathway except for the ICC in the submucosal region (ICC-SM) of the murine proximal colon (Yoneda et al, 2002).…”
Section: Introductionmentioning
confidence: 99%