González R, Arruzazabala M L, Sarracent J
Department of Pharmacology and Toxicology, National Center of Scientific Research, Havana, Cuba.
Allergol Immunopathol (Madr). 1987 Nov-Dec;15(6):361-3.
In former papers we have provided evidence on the protective effect of disodium cromoglycate (DSCG) and ketotifen (Ke) against the contractions induced by various agonists (histamine, serotonin, acetylcholine, prostaglandins) in ileal and tracheal smooth muscle of guinea pigs. To offer an insight into the mode of action of these antiallergic drugs we quantified concentrations of cyclic AMP and GMP in these tissues. We observed that DSCG (10(-3)-10(-2) M) significantly diminished the concentration of cyclic AMP in ileum and trachea of guinea pigs, but it increased the level of cyclic GMP in ileum. Ketotifen (10(-6)-10(-4) M) does not modify cAMP and cGMP in ileum, however, in trachea it significantly decreases the concentrations of cGMP. We also studied the effects of oxatomide, ICI 74.917 and BRL 10.833 on cyclic nucleotides concentrations in guinea pig ileum BRL 10.833 increases cAMP at a relatively high dose (10(-4) M). ICI 74.917 at the same dose decreases cGMP. Oxatomide (10(-6)-10(-4) M) does not modify concentrations of both nucleotides. Our results demonstrate that these antiallergic drugs do not have a unique effect on cyclic nucleotides. Our findings do not support a relevant role of these nucleotides on the mechanism of action of these antiallergic drugs.
在之前的论文中,我们已提供证据表明色甘酸钠(DSCG)和酮替芬(Ke)对豚鼠回肠和气管平滑肌中由各种激动剂(组胺、5-羟色胺、乙酰胆碱、前列腺素)诱导的收缩具有保护作用。为深入了解这些抗过敏药物的作用方式,我们对这些组织中的环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)浓度进行了定量。我们观察到,DSCG(10⁻³ - 10⁻² M)显著降低了豚鼠回肠和气管中cAMP的浓度,但却提高了回肠中cGMP的水平。酮替芬(10⁻⁶ - 10⁻⁴ M)对回肠中的cAMP和cGMP没有影响,然而,在气管中它显著降低了cGMP的浓度。我们还研究了奥沙米特、ICI 74.917和BRL 10.833对豚鼠回肠中环核苷酸浓度的影响。BRL 10.833在相对高剂量(10⁻⁴ M)时会增加cAMP。相同剂量下的ICI 74.917会降低cGMP。奥沙米特(10⁻⁶ - 10⁻⁴ M)对两种核苷酸的浓度均无影响。我们的结果表明,这些抗过敏药物对环核苷酸没有独特的作用。我们的发现不支持这些核苷酸在这些抗过敏药物作用机制中发挥相关作用。