Blebbistatin: use as inhibitor of muscle contraction TeX Export

@article{citeulike:3168357, abstract = {Abstract\ \ Blebbistatin (BLEB) is a recently discovered compound that inhibits myosin-II ATPase activity. In this study, we tested BLEB in intact and skinned isolated rat cardiac trabeculae, rat intact myocytes, and single rabbit psoas myofibrils. BLEB (10\ μM) reduced twitch force and cell shortening that was reversed by exposure to light. BLEB treatment of skinned trabeculae in the dark (1\ hr) reduced Ca2+-activated force \$\$\left( {{\text{EC}}\_{50} = 0.38 \pm 0.03\;{\text{ \$ \mu \$ M}}} \right)\$\$. Rapid (\<5\ ms) BLEB application in Ca2+-activated rabbit myofibrils reduced force proportional to [BLEB]. Two-photon Indo1-AM ratio-metric confocal line-scan microscopy revealed no impact of BLEB on the cytosolic Ca2+ transient. BLEB reduced contractile force in skinned trabeculae without affecting tension-dependent myofilament ATPase activity. We conclude that BLEB specifically uncouples cardiac myofilament activation from Ca2+ activation without affecting EC coupling or cross-bridge cycling parameters. This agent could be useful to uncouple myofilament contractility from electrical events that lead to sarcoplasmic reticulum Ca2+ release in the cardiac myocyte (uncoupling agent) However, the compound is very sensitive to light, a property that limits its application to mechanistic physiological studies.}, author = {Farman, Gerrie and Tachampa, Kittipong and Mateja, Ryan and Cazorla, Olivier and Lacampagne, Alain and de Tombe, Pieter}, citeulike-article-id = {3168357}, citeulike-linkout-0 = {http://dx.doi.org/10.1007/s00424-007-0375-3}, day = {24}, doi = {10.1007/s00424-007-0375-3}, journal = {Pfl\"{u}gers Archiv European Journal of Physiology}, keywords = {blebbistatin, mechanism-of-action, rabbit, rat}, month = {March}, number = {6}, pages = {995--1005}, posted-at = {2008-08-28 01:30:26}, priority = {0}, title = {Blebbistatin: use as inhibitor of muscle contraction}, url = {http://dx.doi.org/10.1007/s00424-007-0375-3}, volume = {455}, year = {2008} }

TY - JOUR ID - citeulike:3168357 L3 - citeulike-article-id:3168357 N2 - Abstract  Blebbistatin (BLEB) is a recently discovered compound that inhibits myosin-II ATPase activity. In this study, we tested BLEB in intact and skinned isolated rat cardiac trabeculae, rat intact myocytes, and single rabbit psoas myofibrils. BLEB (10 μM) reduced twitch force and cell shortening that was reversed by exposure to light. BLEB treatment of skinned trabeculae in the dark (1 hr) reduced Ca2+-activated force $$\left( {{\text{EC}}_{50} = 0.38 \pm 0.03\;{\text{ $ \mu $ M}}} \right)$$. Rapid (<5 ms) BLEB application in Ca2+-activated rabbit myofibrils reduced force proportional to [BLEB]. Two-photon Indo1-AM ratio-metric confocal line-scan microscopy revealed no impact of BLEB on the cytosolic Ca2+ transient. BLEB reduced contractile force in skinned trabeculae without affecting tension-dependent myofilament ATPase activity. We conclude that BLEB specifically uncouples cardiac myofilament activation from Ca2+ activation without affecting EC coupling or cross-bridge cycling parameters. This agent could be useful to uncouple myofilament contractility from electrical events that lead to sarcoplasmic reticulum Ca2+ release in the cardiac myocyte (uncoupling agent) However, the compound is very sensitive to light, a property that limits its application to mechanistic physiological studies. IS - 6 JF - Pflügers Archiv European Journal of Physiology EP - 1005 TI - Blebbistatin: use as inhibitor of muscle contraction VL - 455 SP - 995 KW - blebbistatin KW - mechanism-of-action KW - rabbit KW - rat AU - Farman, Gerrie AU - Tachampa, Kittipong AU - Mateja, Ryan AU - Cazorla, Olivier AU - Lacampagne, Alain AU - de Tombe, Pieter PY - 2008/03/24/ UR - http://dx.doi.org/10.1007/s00424-007-0375-3 ER -