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1.
Syed Naeemuddin Gilani Arif‐ullah Khan Anwarul Hassan Gilani 《Phytotherapy research : PTR》2010,24(4):553-558
This study describes the gut, airways and cardiovascular modulatory activities of Zanthoxylum armatum DC. (Rutaceae) to rationalize some of its medicinal uses. The crude extract of Zanthoxylum armatum (Za.Cr) caused concentration‐dependent relaxation of spontaneous and high K+ (80 mM)‐induced contractions in isolated rabbit jejunum, being more effective against K+ and suggestive of Ca++ antagonist effect, which was confirmed when pretreatment of the tissues with Za.Cr shifted Ca++ concentration‐response curves to the right, like that caused by verapamil. Za.Cr inhibited the castor‐oil‐induced diarrhea in mice at 300–1000 mg/kg. In rabbit tracheal preparations, Za.Cr relaxed the carbachol (1 μM) and high K+‐induced contractions, in a pattern similar to that of verapamil. In isolated rabbit aortic rings, Za.Cr exhibited vasodilator effect against phenylephrine (1 μM) and K+‐induced contractions. When tested in guinea pig atria, Za.Cr caused inhibition of both atrial force and rate of spontaneous contractions, like that caused by verapamil. These results indicate that Zanthoxylum armatum exhibits spasmolytic effects, mediated possibly through Ca++ antagonist mechanism, which provides pharmacological base for its medicinal use in the gastrointestinal, respiratory and cardiovascular disorders. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
2.
Studies on Bronchodilator Activity of Salvia officinalis (Sage): Possible Involvement of K+ Channel Activation and Phosphodiesterase Inhibition 下载免费PDF全文
Anwarul‐Hassan Gilani Najeeb‐ur Rehman Aslam Khan Khalid M. Alkharfy 《Phytotherapy research : PTR》2015,29(9):1323-1329
The aqueous methanolic extract of the aerial parts of Salvia officinalis (So.Cr) was studied to provide possible underlying mechanism(s) for its medicinal use in asthma using the in vivo bronchodilatory assay and isolated tracheal preparations. S. officinalis (1–10 mg/kg) dose‐dependently inhibited carbachol (CCh)‐induced bronchospasm in anesthetized rats with three‐fold greater potency than the positive control, aminophylline. In tracheal preparations, So.Cr inhibited the low K+ (25 mM)‐induced contractions. Pretreatment of the tissues with 4‐aminopyridine reversed the inhibitory effect of the plant extract against low K+, whereas glibenclamide did not show any effect, thus showing the involvement of voltage‐sensitive K+ channels. When tested against the CCh‐induced pre‐contractions for the involvement of any additional mechanism, interestingly, the extract showed a dose‐dependent (0.03–0.1 mg/mL) inhibitory effect and shifted the inhibitory concentration response curves of isoprenaline to the left, thus showing phosphodiesterase enzyme inhibitory‐like action, similar to that of papaverine. These results indicate that the crude extract of S. officinalis possesses bronchodilatory activity mediated predominantly via activation of voltage‐dependent K+ channels and inhibition of phosphodiesterase enzyme; thus, this study provides sound pharmacological basis for its medicinal use in hyperactive airways disorders such as asthma and cough. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
3.
Dual Inhibition of Ca+2 Influx and Phosphodiesterase Enzyme Provides Scientific Base for the Medicinal Use of Chrozophora prostrata Dalz. in Respiratory Disorders 下载免费PDF全文
Usman Arshad Samra Bashir Najeeb ‐ur‐Rehman Tahir Yaqub Anwarul‐Hassan Gilani 《Phytotherapy research : PTR》2016,30(6):1010-1015
The crude ethanolic extract of Chrozophora prostrata (Cp.Cr) was tested using in vivo and ex vivo assays for its possible bronchodilatory effects in order to validate its medicinal use in respiratory disorders, like asthma and cough. Cp.Cr exhibited dose‐dependent inhibition of carbachol (CCh)‐induced bronchospasm in anesthetized rats, similar to aminophylline. When tested on guinea‐pig tracheal preparations, Cp.Cr caused relaxation of both CCh (1 μM) and high K+ (80 mM)‐induced contractions with comparable potencies, similar to papaverine, a dual inhibitor of phosphodiesterse (PDE) and Ca+2 influx. Pre‐treatment of the tracheal tissues with Cp.Cr resulted in potentiation of the inhibitory effect of isoprenaline on CCh‐induced contractions, like that caused by papaverine indicative of PDE inhibitory activity, which was confirmed when Cp.Cr concentration dependently (1 and 3 mg/mL) increased intracellular cAMP levels of the tracheal preparations, like papaverine. Cp.Cr shifted concentrationresponse curves of Ca+2 constructed in guinea‐pig tracheal preparation towards right with suppression of the maximum response, similar to both verapamil and papaverine. These data indicate bronchodilator activity of Chrozophora prostrata mediated possibly through dual inhibition of PDE and Ca+2 influx, thus, showing therapeutic potential in asthma with effect enhancing and side‐effect neutralizing potential Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
4.
功能性胃肠病(FGIDs)症状重叠现象在临床上非常普遍,增加了临床诊治的难度。调中复衡理论是在继承脾胃学说和通降论学术思想的基础上,结合长期临床实践所构建的脾胃病治疗理论。基于调中复衡理论,认为脾胃功能失调、气机升降失衡是FGIDs症状重叠现象发生的核心病机,其治疗目标是恢复气机升降平衡及脏腑功能平衡的"两平衡"状态,辨治则以"八纲通胃法"作为具体方法,即以脏腑为纲、多脏腑同调为主,以气血为纲、调气复通降为要,以虚实为纲、补虚泻实为法,以寒热为纲、平调寒热为常。以调中复衡理论为指导,纲目分明,执简驭繁,可为临床诊治FGIDs症状重叠厘清思路。 相似文献
5.
Iva Mucalo Elena Jovanovski Dario Rahelić Velimir Božikov Željko Romić Vladimir Vuksan 《Journal of ethnopharmacology》2013