Quirion R, Regoli D, Rioux F, St-Pierre S
Br J Pharmacol. 1979 Jun;66(2):251-7. doi: 10.1111/j.1476-5381.1979.tb13673.x.
1 Somatostatin (SS) was evaluated as a chronotropic and inotropic agent in isolated spontaneously beating auricles of rats, rabbits and guinea-pigs.2 SS was completely inactive in rat and rabbit auricles but exerted a dose-dependent, negative inotropic effect in guinea-pig auricles in concentrations between 1.5 x 10(-8) to 1.2 x 10(-6) M.3 The negative inotropic effect of SS (6.0 x 10(-8) and 3.0 x 10(-7) M) was not inhibited by a mixture of antagonists containing practolol (7.9 x 10(-6) M), phentolamine (3.5 x 10(-7) M), methysergide (2.8 x 10(-7) M), diphenhydramine (3.9 x 10(-5) M), cimetidine (4.0 x 10(-5) M) atropine (3.4 x 10(-7) M) and indomethacin (1.4 x 10(-5) M).4 The negative inotropic effect of SS was greatly potentiated by reduction in the Ca(2+) concentration of the medium from 5.0 to 1.25 mM.5 On a molar basis, SS was equipotent with acetylcholine (ACh) as a negative inotropic agent in the guinea-pig auricles.6 SS (6.0 x 10(-8) and 6.0 x 10(-7) M) was found to inhibit selectively the positive inotropic action of neurotensin (NT) in guinea-pig but not in rat auricles.7 The inhibitory action of SS against NT was independent of its negative inotropic action.8 These results suggest that SS produces its negative inotropic action by interacting with specific receptors presumably located in the cell membrane of guinea-pig atria. The interaction between SS and its receptor may cause a decreased Ca(2+) diffusion and/or transport into the atrial cells. The physiological and pharmacological significance of these results is discussed.
1 在大鼠、兔和豚鼠的离体自发搏动心房中,对生长抑素(SS)作为变时性和变力性药物进行了评估。
2 SS对大鼠和兔心房完全无活性,但在豚鼠心房中,浓度在1.5×10⁻⁸至1.2×10⁻⁶ M之间时,会产生剂量依赖性的负性肌力作用。
3 SS(6.0×10⁻⁸和3.0×10⁻⁷ M)的负性肌力作用不受含有醋氨心安(7.9×10⁻⁶ M)、酚妥拉明(3.5×10⁻⁷ M)、甲基麦角新碱(2.8×10⁻⁷ M)、苯海拉明(3.9×10⁻⁵ M)、西咪替丁(4.0×10⁻⁵ M)、阿托品(3.4×10⁻⁷ M)和消炎痛(1.4×10⁻⁵ M)的拮抗剂混合物的抑制。
4 当培养基中Ca²⁺浓度从5.0 mM降至1.25 mM时,SS的负性肌力作用大大增强。
5 在豚鼠心房中,按摩尔计算,SS作为负性肌力药物与乙酰胆碱(ACh)等效。
6 发现SS(6.0×10⁻⁸和6.0×10⁻⁷ M)在豚鼠心房中选择性抑制神经降压素(NT)的正性肌力作用,但在大鼠心房中无此作用。
7 SS对NT的抑制作用与其负性肌力作用无关。
8 这些结果表明,SS通过与可能位于豚鼠心房细胞膜上的特异性受体相互作用产生其负性肌力作用。SS与其受体之间的相互作用可能导致Ca²⁺向心房细胞内的扩散和/或转运减少。讨论了这些结果的生理和药理意义。