Kentish J C, Davey R, Largen P
Department of Pharmacology, U.M.D.S., St. Thomas's Hospital, London, UK.
Pflugers Arch. 1992 Aug;421(5):519-21. doi: 10.1007/BF00370267.
An alteration in the length of isolated cardiac muscle produces an immediate change in twitch force, then a slow further change in the same direction. We have found that the slow changes in force in rabbit papillary muscles are blocked or reversed by the beta-agonist, isoprenaline (1 microM). The abolition of the slow responses by isoprenaline was not due to saturation of the myofibrils with Ca2+, as the blockade continued if the extracellular [Ca2+] was reduced in the presence of isoprenaline so that twitch force was < 50% maximal. Ryanodine (1 microM) did not block the slow responses, suggesting that the sarcoplasmic reticulum does not mediate the responses. These results suggest that changes of intracellular [cAMP] may mediate, or at least modulate, the slow force responses to a length change in cardiac muscle.
孤立心肌长度的改变会立即引起抽搐力的变化,随后在同一方向上发生缓慢的进一步变化。我们发现,兔乳头肌中力的缓慢变化可被β-激动剂异丙肾上腺素(1微摩尔)阻断或逆转。异丙肾上腺素对缓慢反应的消除并非由于肌原纤维被Ca2+饱和,因为在异丙肾上腺素存在的情况下降低细胞外[Ca2+],使抽搐力<最大抽搐力的50%时,阻断作用仍持续存在。雷诺丁(1微摩尔)并未阻断缓慢反应,这表明肌浆网并不介导这些反应。这些结果表明,细胞内[cAMP]的变化可能介导或至少调节心肌长度变化时的缓慢力反应。