Pittner H
Agents Actions. 1976 Sep;6(5):584-8. doi: 10.1007/BF01971573.
The chronotropic effects of midodrine, glycine (10(-8) to 3.10(-3) M), ST1059 and methoxamine (10(-8) to 10(-3) M) were investigated in the spontaneously beating guinea-pig right atrial preparation. Midodrine and glycine produced a slight, but significant rise in atrial rate over a wide concentration range. The midodrine-induced rise in atrial rate was not influenced by the beta-adrenergic receptor blocking drug propranolol (10(-6) M). The histamine (H2)-receptor blocking drug metiamide (3.10(-5) M) abolished the positive chronotropic actions of both midodrine and glycine. No positive chronotropic effect was seen after the administration of ST 1059 or methoxamine. A decrease in atrial rate was elicited by high concentrations (above 10(-4) to 10(-3) M) of the sympathomimetic agents midodrine, ST 1059, and methoxamine, but not by the amino acid glycine.
在豚鼠右心房自发搏动标本中研究了米多君、甘氨酸(10⁻⁸至3.10⁻³M)、ST1059和甲氧明(10⁻⁸至10⁻³M)的变时作用。米多君和甘氨酸在较宽的浓度范围内使心房率轻度但显著升高。米多君引起的心房率升高不受β-肾上腺素能受体阻断药普萘洛尔(10⁻⁶M)的影响。组胺(H2)受体阻断药甲硫米特(3.10⁻⁵M)消除了米多君和甘氨酸的正性变时作用。给予ST 1059或甲氧明后未观察到正性变时作用。高浓度(高于10⁻⁴至10⁻³M)的拟交感神经药米多君、ST 1059和甲氧明可引起心房率降低,但氨基酸甘氨酸不会。