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Article: Rat skeletal muscle contractility: The role of beta-adrenoceptors and nitric oxide system

Prostran, M., Faculty of Medicine, Belgrade (Serbia) / Stojanović, R., Faculty of Medicine, Belgrade (Serbia) / Todorović Z., Faculty of Medicine, Belgrade (Serbia) / Vučković, S., Faculty of Medicine, Belgrade (Serbia) / Savić-Vujović, K., Faculty of Medicine, Belgrade (Serbia) / Medić, B., Faculty of Medicine, Belgrade (Serbia) / Grajić, M., Clinical Center of Serbia, Belgrade (Serbia). Clinic for Physical and Rehabilitation Medicine / Kadija, M., Clinical Center of Serbia, Belgrade (Serbia). Institute for Orthopaedic Surgery and Traumatology

Acta Veterinaria (Serbia)

(2011)  Volume v. 61, Issue (4), Page(s) p. 339–348

Abstract: Both beta-adrenoceptors and the nitric oxide system play a significant role in the modulation of skeletal muscle contractility. Skeletal muscle adrenoceptors mainly belong to beta2 subtype, while all three types of nitric oxide synthase may influence ... ...

Abstract Both beta-adrenoceptors and the nitric oxide system play a significant role in the modulation of skeletal muscle contractility. Skeletal muscle adrenoceptors mainly belong to beta2 subtype, while all three types of nitric oxide synthase may influence muscle contractility. The aim of our study was to investigate the possible interplay between beta-adrenoceptor agonists and nitric oxide system in the modulation of contractility of isolated rat hemidiaphragm. Adrenaline (0.05-1.5 micromol/L) and noradrenaline (1-5 micromol/L) given in a cumulative manner produced a concentration-related increase in Td. L-NAME (1, 3 and 10 mmol/L; 30 min of incubation) produced a significant, dose-dependent increase in Td of the muscle pretreated with cumulative concentrations of adrenaline (deltaTd up to 16%). When hemidiaphragm was pretreated with noradrenaline instead of adrenaline, L-NAME (3 mmol/L) it produced a similar potentiation of Td. In conclusion, nitric oxide seems to oppose beta-adrenoceptor potentiation of diaphragm contractility, and such an interaction depends on previous adrenoceptor stimulation. Nitric oxide probably decreases beta-adrenoceptor response via cGMP-induced stimulation of phosphodiesterase 2. The interaction between substances which modulate NO system activity and cAMP levels in the skeletal muscle may be of a great clinical importance for the treatment of certain respiratory and neurological diseases.
Keywords RATS ; MUSCLES ; EPINEPHRINE ; HORMONE RECEPTORS ; RAT ; MUSCLE ; ADRANALINE ; RACEPTEUR D'HORMONE ; RATA ; MASCULOS ; EPINEFRINA ; RECEPTORES DE HORMONAS ; http://www.fao.org/aos/agrovoc#c_6464 ; http://www.fao.org/aos/agrovoc#c_5003 ; http://www.fao.org/aos/agrovoc#c_2620 ; http://www.fao.org/aos/agrovoc#c_26875
Language English
Document type Article
ISSN 0567-8315
Database AGRIS - International Information System for the Agricultural Sciences and Technology

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