Pharmacology and toxicology of Atrovent.

A Engelhardt
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Abstract

The anticholinergic drug ipratropium bromide (Atrovent) can be described as having pharmacologically a high degree of activity and a certain bronchoselectivity when administered intravenously. Inhalation studies, however, indicate that this is the most suitable route of administration. Inhalation provides with small doses the most effective concentration locally at the smooth muscle of the airways without producing anticholinergic side effects due to absorption from the airways or from the gastrointestinal tract. In certain experimental models of allergic asthma, ipratropium bromide was shown to be capable of influencing favourably bronchoconstriction and mediator release. Extensive toxicological examinations revealed with high doses all typical symptoms of overdosing an anticholinergic drug, like mydriasis, dryness of the mucosae and meteorism with coprostasis. Acute and long term inhalation studies gave no evidence for a functional and morphological impairment of the lungs and airways.

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Atrovent的药理学和毒理学研究。
抗胆碱能药物异丙托品溴化(Atrovent)在药理学上具有高度的活性,静脉给药时具有一定的支气管选择性。然而,吸入研究表明,这是最合适的给药途径。小剂量吸入在气道平滑肌局部提供最有效的浓度,而不会由于气道或胃肠道的吸收而产生抗胆碱能副作用。在某些过敏性哮喘的实验模型中,异丙托品溴化被证明能够有利地影响支气管收缩和介质释放。广泛的毒理学检查显示,大剂量服用抗胆碱能药物的所有典型症状,如瞳孔肿大、粘膜干燥和伴前列腺炎的血小板增多。急性和长期吸入研究没有证据表明肺和气道的功能和形态学损伤。
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