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Intracellular effect of β3-adrenoceptor agonist Carazolol on skeletal muscle,a direct interaction with SERCA
Institution:1. Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China;2. Department of Nephrology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China;1. Biomedical Engineering Faculty, Technion-IIT, Haifa, Israel;2. College of Life Sciences, Peking University, Beijing, China;3. Laboratory of Cardiovascular Science, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA;1. Department of Clinical Laboratory, Aerospace Central Hospital, Beijing 100049, China;2. Department of Nephrology, Peking University First Hospital, Beijing 100034, China;3. Department of Clinical Laboratory, Peking University First Hospital, Beijing 100034, China;1. Service de radiothérapie, institut de cancérologie et d’hématologie, CHRU Morvan, 2, avenue Foch, 29200 Brest, France;2. Service de médecine nucléaire, CHRU Morvan, 2, avenue Foch, 29200 Brest, France;3. Service de radiothérapie, centre hospitalier de Cornouaille, 14bis, avenue Yves-Thépot, 29107 Quimper cedex, France
Abstract:Carazolol (CZL) is a known agonist of β3 and antagonist of β1 and β2 adrenoceptors (AR), used in the animal production industry to improve meat quality by reducing animal stress and skeletal muscle (SM) proteolysis. Here we sought to better understand the direct effect CZL has on SM. We study CZL effect on calcium (Ca2+) regulation by enzymatic activity kinetics of the Ca2+-ATPase (SERCA), in isolated sarcoplasmic reticulum (SR) from SM and on the mechanical properties of isolated muscle. In isolated SR from SM previously incubated with 0.03 mM CZL, but absent during SR isolation and during SERCA activity determination, the activity was reduced by 45%. Thermal analysis of SERCA activity with CZL shifted the transition temperature of inactivation (Ti) from Ti = 47 to 44 °C. When isolated SR from fast and slow SM was exposed to CZL, inhibition of SERCA occurred in a dose dependent manner. Slow and fast SM Ti of SERCA shifted to a lower temperature in the presence of CZL and a second transition appears at temperatures <40 °C. In isolated extensor digitorum longus (EDL) and soleus muscles, CZL reduces the contraction force and increases susceptibility to fatigue. However, recovery force after fatigue in either muscle was higher. Our results suggest that Carazolol penetrates the plasma membrane and interacts with SERCA, thus having an important effect on skeletal muscle function. The inhibition of SERCA may lead to a decrement in SR Ca2+-release promoting further failure in muscle contraction.
Keywords:Skeletal muscle  SERCA  Carazolol  β3 adrenoceptors  Fatigue
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