Verma S C, McNeill J H
Agents Actions. 1977 Jul;7(2):191-7. doi: 10.1007/BF01969971.
The positive inotropic, chronotropic and cyclic AMP producing effects of tolazoline were studied on atrial and ventricular preparations obtained from guinea pig heart. (1) The direct positive inotropic effects of tolazoline on the paced left atrial preparation from the guinea pig hearts was blocked by promethazine, but not by burimamide. Tolazoline did not elevate cyclic AMP levels in this preparation. (2) Tolazoline produced a positive chronotropic effect which was blocked by burimamide and not by promethazine and caused a 2-3 fold elevation of cyclic AMP in spontaneously beating right atria. (3) Burimamide antagonized the inotropic and cyclic AMP increasing effects of tolazoline on electrically driven ventricular strips. (4) The effects of tolazoline were unchanged by reserpine pretreatment of the guinea pigs or by prior exposure to phentolamine or propranolol. (5) These results suggest that tolazoline can activate both H1 and H2 receptors in the guinea pig heart. Furthermore the data suggests that H2 receptors are present in right atria and ventricle and that such receptors are associated with cyclic AMP. H1 receptors are present in the left atria and are not associated with the cyclic nucleotide.
研究了妥拉唑啉对豚鼠心脏心房和心室标本的正性肌力、变时性及产生环磷酸腺苷(cAMP)的作用。(1)豚鼠心脏起搏左心房标本上,妥拉唑啉的直接正性肌力作用被异丙嗪阻断,但不被丁咪胺阻断。妥拉唑啉未使该标本中的cAMP水平升高。(2)妥拉唑啉产生变时性正性效应,此效应被丁咪胺阻断而不被异丙嗪阻断,且使自发搏动的右心房中的cAMP升高2 - 3倍。(3)丁咪胺拮抗妥拉唑啉对电驱动心室肌条的正性肌力及cAMP增加作用。(4)豚鼠经利血平预处理或事先接触酚妥拉明或普萘洛尔后,妥拉唑啉的作用未改变。(5)这些结果提示,妥拉唑啉可激活豚鼠心脏中的H1和H2受体。此外,数据表明H2受体存在于右心房和心室,且此类受体与cAMP相关。H1受体存在于左心房,与环核苷酸无关。