期刊
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
卷 314, 期 3, 页码 1386-1392出版社
AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS
DOI: 10.1124/jpet.105.087742
关键词
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资金
- NHLBI NIH HHS [R01-HL63713] Funding Source: Medline
Pretreatment with D-myo-inositol-1,4,5-trisphosphate hexasodium (D-myo-IP3), the sodium salt of the second messenger inositol 1,4,5-trisphosphate (IP3), is cardioprotective and triggers a reduction of infarct size comparable in magnitude to that obtained with ischemic preconditioning. However, this observation is enigmatic; whereas IP3 signaling is conventionally initiated by receptor binding, IP3 receptors are typically considered to be intracellular, and D-myo-IP3 is membrane-impermeable. We propose that this paradox is explained by the presence of poorly characterized external IP3 receptors and hypothesize that: 1) infarct size reduction with D-myo-IP3 is receptor-mediated; and 2) communication via gap junctions and/or hemichannels is required to initiate this protection. To investigate the role of receptor binding, isolated buffer-perfused rabbit hearts underwent 30 min of coronary occlusion (CO) and 2 h of reflow. Prior to CO, hearts received no treatment (controls), D-myo-IP3, L-myo-IP3 (enantiomer not recognized by the IP3 receptor), D-myo-IP3 + the IP3 receptor inhibitor xestospongin C (XeC), or XeC alone. Infarct size, assessed by tetrazolium staining, was reduced with D-myo-IP3 treatment, whereas hearts that received L-myo-IP3 or D-myo-IP3 + XeC showed no protection. To evaluate the contribution of gap junctions/hemichannels, additional control and D-myo-IP3-treated cohorts received a 5-min infusion of heptanol or Gap 27, two structurally distinct gap junction inhibitors, administered at doses confirmed to attenuate intercellular transmission of a gap junction-permeable fluorescent dye. There was no infarct-sparing effect of D-myo-IP3 in inhibitor-treated hearts. These data support the concepts that infarct size reduction with D-myo-IP3 is triggered by receptor binding and that communication via gap junctions/hemichannels is involved in initiating this protection.
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