Adrenomedullin inhibits ovalbumin-induced bronchoconstriction and airway microvascular leakage in guinea-pigs

Human adrenomedullin is a potent vasodilator with bronchodilation propertie s. The effects of adrenomedullin on antigen-induced bronchoconstriction and airway microvascular leakage in guinea-pigs was investigated. The portion of the adrenomedullin molecule possessing these pulmonary active profiles w as also examined, using two truncated adrenomedullin molecules: adrenomedul lin (1-25) and adrenomedullin (22-52). Four weeks after sensitization with ovalbumin (0.1 mg.kg(-1)), the guinea-p igs were anaesthetized and mechanically ventilated. Respiratory resistance, dynamic compliance and arterial blood pressure were monitored. Airway micr ovascular leakage was evaluated by extravasation of 20 mg.kg(-1) Evans blue into airway interstitial tissue. In order to enhance the pulmonary effects of adrenomedullin, the active production of endogenous nitric oxide was in hibited by coadministration of a nitric oxide synthase inhibitor, L-N-G-nit roarginine methethyl ester (10 mg.kg(-1)). Intravenous pretreatment with adrenomedullin (10, 30 and 100 mu g.mL(-1)) d ose-dependently inhibited ovalbumin-induced bronchoconstriction and airway microvascular leakage in all airway segments. Inhaled adrenomedullin (100 m u g.mL(-1), 1 min) also significantly inhibited pulmonary changes induced b y ovalbumin inhalation (3 mg.mL(-1), 3 min). These pulmonary profiles of ad renomedullin were enhanced by inhibiting the active production of endogenou s nitric oxide. In conclusion, adrenomedullin has inhibitory effects on antigen-induced mic rovascular leakage and bronchoconstriction in guinea-pigs. These beneficial effects strongly related to its unique ring structure and N-terminal segme nt, making it a potential anti-asthma.