Neurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iran AND Department of Clinical Pharmacy, School of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Department of Physiology, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
Iran J Allergy Asthma Immunol. 2020 Aug 25;19(4):386-396. doi: 10.18502/ijaai.v19i4.4113.
This study was conducted to evaluate the possible mechanisms of the relaxant effects of hydroalcoholic extract of Plantago major (P. major) on tracheal smooth muscle (TSM) in rats. The effects of cumulative concentrations of P. major (5, 10, 20 and 40 mg/mL) and theophylline (0.2, 0.4, 0.6 and 0.8 mM) were evaluated on pre-contracted TSM with 10 μΜ methacholine or 60 mM KCl. To determine the possible mechanisms, the relaxant effect of the plant was also examined on incubated TSM with atropine, indomethacin, chlorpheniramine, glibenclamide, diltiazem, papaverine, and propranolol. The results indicated concentration-dependent relaxant effects for P. major in non-incubated TSM contracted by methacholine or KCl. There was no statistically significant difference in the relaxant effects of P. major between non-incubated and incubated tissues with indomethacin, papaverine, and propranolol. However, the relaxant effects of P. major in incubated tissues with atropine (p<0.01 to p<0.001), chlorpheniramine (p<0.05 to p<0.001), glibenclamide (p<0.05), or diltiazem (p<0.01) were significantly lower than non-incubated TSM. P. major indicated relatively potent relaxant effects which were lower than those of theophylline. Muscarinic and histamine (H1) receptors inhibition, as well as calcium channel blocking and potassium channel opening effects are suggested to contribute to the TSM relaxant effect of the plant.
这项研究旨在评估车前草(Plantago major)水醇提取物对大鼠气管平滑肌(TSM)松弛作用的可能机制。评估了车前草(5、10、20 和 40 mg/mL)和茶碱(0.2、0.4、0.6 和 0.8 mM)的累积浓度对 10 μΜ 乙酰甲胆碱或 60 mM KCl 预收缩的 TSM 的影响。为了确定可能的机制,还研究了植物对孵育的 TSM 中阿托品、吲哚美辛、氯苯那敏、格列本脲、地尔硫卓、罂粟碱和普萘洛尔的松弛作用。结果表明,车前草对乙酰甲胆碱或 KCl 收缩的非孵育 TSM 具有浓度依赖性的松弛作用。在吲哚美辛、罂粟碱和普萘洛尔存在下,非孵育和孵育组织中车前草的松弛作用无统计学差异。然而,在孵育组织中,车前草对阿托品(p<0.01 至 p<0.001)、氯苯那敏(p<0.05 至 p<0.001)、格列本脲(p<0.05)或地尔硫卓(p<0.01)的松弛作用明显低于非孵育 TSM。车前草表现出相对较强的松弛作用,但其强度低于茶碱。提示 M 型胆碱能受体和组胺(H1)受体抑制、钙通道阻断和钾通道开放作用可能有助于该植物对 TSM 的松弛作用。