首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >7-Epiclusianone, a tetraprenylated benzophenone, relaxes airway smooth muscle through activation of the nitric oxide-cGMP pathway.
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7-Epiclusianone, a tetraprenylated benzophenone, relaxes airway smooth muscle through activation of the nitric oxide-cGMP pathway.

机译:7-Epiclusianone是一种四烯丙基化的二苯甲酮,可通过激活一氧化氮-cGMP途径使气道平滑肌松弛。

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摘要

This study was undertaken to investigate the putative mechanism(s) underlying the antispasmodic effect of 7-epiclusianone, a naturally occurring compound isolated from the plant Garcinia brasiliensis. Guinea pig tracheal rings were mounted in tissue baths filled with Krebs' solution, and the contractile response to distinct stimuli was measured in the presence or absence of 7-epiclusianone. We also tested the effect of 7-epiclusianone on methacholine-evoked airways obstruction in BALB/c mice using barometric plethysmography. 7-Epiclusianone (10 microM) inhibited epithelium-intact tracheal ring contraction induced by allergen, histamine, 5-hydroxytryptamine, or carbachol challenge. The relaxation effect was abrogated by epithelium removal, the presence of nitric-oxide synthase inhibitor N(omega)-nitro-L-arginine methyl ester (L-NAME) (100 microM), or soluble guanylate cyclase inhibitor 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ) (10 microM). 7-Epiclusianone (1-100 microM) induced a dose-dependent increase in the intracellular cGMP levels of cultured tracheal rings. The relaxation effect of 7-epiclusianone was also inhibited by K(+) channel blockers tetraethylammonium (10 microM), glibenclamide (1 microM), or apamin (1 microM), but not by 9-(tetrahydro-2'-furyl)adenine (SQ22,536) (100 microM), an adenylate cyclase inhibitor. In epithelium-intact tracheal rings, 7-epiclusianone also inhibited Ca(2+)-induced contractions in K(+) (60 mM)-depolarized preparations, but it seemed ineffective in assays in which epithelium-denuded tracheal ring preparations were used. Oral administration of 7-epiclusinone (25-100 mg/kg) dose-dependently inhibited airway obstruction triggered by aerosolized methacholine (6-25 mg/ml), in a mechanism sensitive to L-NAME (20 mg/kg). In conclusion, the relaxation effect of 7-epiclusinone seems to be mediated by epithelium-, nitric oxide-, and cGMP-dependent mechanisms. Furthermore, oral administration of 7-epiclusianone reduces episodes of bronchial obstruction, warranting further research on this compound regarding a putative application in asthma therapy.
机译:进行这项研究是为了研究推测的7-表皮松酮的抗痉挛作用的潜在机制,该物质是从巴西藤黄植物中分离得到的天然化合物。将豚鼠气管环固定在装有Krebs溶液的组织浴中,并在存在或不存在7-表皮松酮的情况下测量对不同刺激的收缩反应。我们还使用气压体积描记法在BALB / c小鼠中测试了7-表氯尿酮对乙酰甲胆碱诱发的气道阻塞的作用。 7-Epiclusianone(10 microM)抑制了变应原,组胺,5-羟基色胺或卡巴胆碱激发的上皮完整气管环收缩。松弛效应被上皮去除,一氧化氮合酶抑制剂N(ω)-硝基-L-精氨酸甲酯(L-NAME)(100 microM)或可溶性鸟苷酸环化酶抑制剂1H- [1,2 ,4]恶二唑并[4,3-a]喹喔啉-1-酮(ODQ)(10 microM)。 7-Epiclusianone(1-100 microM)诱导了气管环细胞内cGMP水平的剂量依赖性增加。 K-(+)通道阻滞剂四乙铵(10 microM),格列苯脲(1 microM)或阿帕明(1 microM)也抑制7-表氯安酮的松弛作用,但9-(tetrahydro-2'-furyl)腺嘌呤则没有抑制作用(SQ22,536)(100 microM),一种腺苷酸环化酶抑制剂。在上皮完整的气管环,7-epiclusianone还抑制了Ca(2+)诱导的K(+)(60 mM)去极化的制剂中的收缩,但在使用上皮裸露的气管环制剂的测定中似乎无效。以对L-NAME(20 mg / kg)敏感的机制,口服7-表皮松酮(25-100 mg / kg)剂量依赖性抑制气雾化乙酰甲胆碱(6-25 mg / ml)触发的气道阻塞。总之,7-表皮松酮的松弛作用似乎是由上皮,一氧化氮和cGMP依赖性机制介导的。此外,口服7-表氯尿酮可减少支气管阻塞的发作,因此有必要对该化合物进行有关哮喘治疗的推定应用的进一步研究。

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