1997
DOI: 10.1016/s0024-3205(97)00604-8
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Types of potassium channels involved in coronary reactive hyperemia depend on duration of preceding ischemia in rat hearts

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Cited by 14 publications
(22 citation statements)
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“…Reactive-hyperemia to 5 min vascular occlusion is inhibited by both TEA and charybdotoxin in isolated rat hearts (1302). Block of BK Ca channels with TEA in the pig coronary circulation resulted in a decrease in resting vascular conductance and a decrease in exercise-induced hyperemia (996).…”
Section: Bkca Channelsmentioning
confidence: 99%
See 1 more Smart Citation
“…Reactive-hyperemia to 5 min vascular occlusion is inhibited by both TEA and charybdotoxin in isolated rat hearts (1302). Block of BK Ca channels with TEA in the pig coronary circulation resulted in a decrease in resting vascular conductance and a decrease in exercise-induced hyperemia (996).…”
Section: Bkca Channelsmentioning
confidence: 99%
“…Glibenclamide also inhibited reactive hyperemia induced by 15 to 120 s occlusion in canine coronary circulation, in vivo (73, 128, 262, 352, 654, 728, 780, 1569). Similarly, glibenclamide inhibits reactive hyperemia induced by 30 s occlusion in isolated rat hearts (1302). Reactive hyperemia also was reduced by 30% after 5 min occlusion in pig hearts, in vivo (1605).…”
Section: Katp Channelsmentioning
confidence: 99%
“…PORH refers to the phenomenon of increased BF that follows relief of ischaemia and is a result of dilation of resistance vessels. This vasodilation has been attributed to myogenic relaxation of the vessels [20] and local release of mediators and metabolites such as adenosine [21], prostaglandins and nitric oxide [1,22]. Measuring PORH is frequently used to evaluate structural changes in the circulation [23].…”
Section: Introductionmentioning
confidence: 99%
“…TEA is a non-selective K + channel blocker; thus it can block calcium-activated K + channels (K ca ) at concentrations as low as 1 m M [32] . However, high concentrations may be required to block other voltage-dependent K + channels, such as K ATP channels, because a TEA concentration of 20 m M is typically used for in vitro electrophysiology experiments [33,34] . Therefore, the proliferative inhibition of TEA may be due to the blockade of K ca channels, while the blockade of other voltage-dependent K + channels, such as the K ATP channels, may contribute to the apoptotic effect.…”
Section: Discussionmentioning
confidence: 99%