Behrouz Sepideh, Memarzia Arghavan, Eshaghi Ghalibaf Mohammad Hossein, Boskabady Mohammad Hossein
Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Physiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Iran J Basic Med Sci. 2024;27(10):1317-1322. doi: 10.22038/ijbms.2024.77720.16822.
In the present study, the relaxant effect of crocetin on tracheal smooth muscle cells (TSM) and its possible mechanisms were evaluated.
The study was conducted on 54 male Wistar rats in 8 groups. TSM was contracted by methacholine (10 μM) and KCl (60 mM), and the relaxant effects of four cumulative concentrations of crocetin, petal extract of saffron, and theophylline were examined on non-incubated and TSM incubated with propranolol, chlorpheniramine, diltiazem, atropine, glibenclamide, and indomethacin were investigated.
In non-incubated TSM contracted by methacholine or KCl, crocetin and theophylline showed concentration-dependent relaxant effects (all, <0.001). However, various concentrations of crocetin showed significantly lower relaxant effects compared to those of theophylline (all, <0.001). In the methacholine-induced contraction of TSM, the relaxation effect of the last concentration of crocetin in the TSM incubated with propranolol was lower than in non-incubated TSM (<0.05). In the incubated TSM with chlorpheniramine, the relaxant effects of the two last concentrations of crocetin were significantly lower than in the non-incubated tissues contracted by KCl (<0.05 and <0.0). The levels of EC50 crocetin in the incubated TSM with glibenclamide, chlorpheniramine, and indomethacin were markedly lower than in non-incubated (all, <0.05).
The results showed potent relaxation effects of crocetin on TSM and were suggested to be through stimulation of ß-adrenergic receptors, inhibition of histamine (H) receptors, and potassium channel opening mechanisms.
在本研究中,评估了西红花酸对气管平滑肌细胞(TSM)的舒张作用及其可能机制。
本研究对8组54只雄性Wistar大鼠进行。用乙酰甲胆碱(10μM)和氯化钾(60mM)使TSM收缩,检测了四种累积浓度的西红花酸、藏红花花瓣提取物和茶碱对未孵育的TSM以及与普萘洛尔、氯苯那敏、地尔硫卓、阿托品、格列本脲和吲哚美辛孵育后的TSM的舒张作用。
在由乙酰甲胆碱或氯化钾收缩的未孵育TSM中,西红花酸和茶碱呈现浓度依赖性舒张作用(均P<0.001)。然而,与茶碱相比,不同浓度的西红花酸舒张作用显著更低(均P<0.001)。在乙酰甲胆碱诱导的TSM收缩中,与普萘洛尔孵育后的TSM中,西红花酸最后一个浓度的舒张作用低于未孵育的TSM(P<0.05)。在与氯苯那敏孵育的TSM中,西红花酸最后两个浓度的舒张作用显著低于由氯化钾收缩的未孵育组织(P<0.05和P<0.0)。与格列本脲、氯苯那敏和吲哚美辛孵育后的TSM中,西红花酸的半数有效浓度(EC50)水平显著低于未孵育的TSM(均P<0.05)。
结果表明西红花酸对TSM有强大的舒张作用,提示其作用机制可能是通过刺激β-肾上腺素能受体、抑制组胺(H)受体以及开放钾通道机制。