首页> 外文期刊>Journal of Plant Biology >Comparison of Endothelium-Dependent Vasorelaxation of Crude Ginsenosides from Mountain-Grown Ginseng and Red Ginseng
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Comparison of Endothelium-Dependent Vasorelaxation of Crude Ginsenosides from Mountain-Grown Ginseng and Red Ginseng

机译:山参和红参粗人参皂苷内皮依赖性血管舒张作用的比较

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摘要

Mountain-grown ginseng (Panax ginseng C. A. Meyer; Sansam in Korean) is believed to possess more potent biological activity than red ginseng. This study examined the endothelium-dependent vasorelaxant effects and possible mechanisms of crude ginsenosides from adventitious roots of Korean mountain-grown ginseng (GS-ARMG) and red ginseng (GS-RG) in isolated rat aorta pre-contracted with norepinephrine. GS-ARMG (0.03-3.0 mg/mL) produced transient acute relaxation in a concentration-dependent manner, with a maximum relaxation (mean +/- SEM) of 90 +/- 9% and a median effective concentration (EC50) of 0.09 +/- 0.07 mg/mL. GS-ARMG displayed about 25-fold more potent activity than GS-RG (maximum relaxation 50 +/- 4%, EC50 2.34 +/- 1.30 mg/mL). Relaxations induced by both GS-ARMG (1.0 mg/mL) and GS-RG (1.0 mg/mL) were nearly abolished by endothelial ablation or pre-treatment with N (G) -nitro-l-arginine, a nitric oxide synthase inhibitor, or by methylene blue, a soluble guanylate cyclase inhibitor. These inhibitory effects, however, revealed different sensitivity of GS-ARMG and GS-RG; the maximum relaxations attained were 30-38% and 13-17% that of untreated preparations, respectively, but indomethacin and cyclooxygenase inhibitors did not affect the response. None of the receptor antagonists, atropine, diphenhydramine, [D-Pro(2), D-Trp(7, 9)]-substance P, or propranolol, caused any significant inhibition to GS-ARMG-induced relaxation; however, atropine or propranolol caused a 10% reduction in the relaxation, suggesting possible involvement of a muscarinic receptor or a beta-adrenoceptor in the GS-ARMG-induced relaxation. These results demonstrate that GS-ARMG produces endothelium-dependent relaxation of isolated rat aorta similar to that of GS-RG; increased nitric oxide production and increased vascular levels of cGMP in endothelial cells could contribute to the relaxation. However, GS-ARMG has more potent activity than GS-RG to relax isolated rat aorta though an active substance(s), which might be higher in mountain-grown ginseng due to the growing conditions on mountains or the processing during manufacture of GS-ARMG. These factors may contribute to understanding the biological beneficial effects of mountain-grown ginseng.
机译:据信山地人参(Panax ginseng C. A. Meyer;韩国的Sansam)比红参具有更强的生物活性。这项研究检查了由去甲肾上腺素预先提取的大鼠主动脉中,韩国山参(GS-ARMG)和红参(GS-RG)的不定根中的内皮依赖性血管舒张作用和粗制人参皂苷的可能机制。 GS-ARMG(0.03-3.0 mg / mL)以浓度依赖性的方式产生短暂的急性松弛,最大松弛(平均+/- SEM)为90 +/- 9%,中位有效浓度(EC50)为0.09 +/- 0.07毫克/毫升GS-ARMG的活性比GS-RG高25倍(最大松弛50 +/- 4%,EC50 2.34 +/- 1.30 mg / mL)。 GS-ARMG(1.0 mg / mL)和GS-RG(1.0 mg / mL)诱导的松弛作用通过内皮消融或用一氧化氮合酶抑制剂N(G)-硝基-1-精氨酸预处理几乎被消除或亚甲基蓝,一种可溶性鸟苷酸环化酶抑制剂。然而,这些抑制作用揭示了GS-ARMG和GS-RG的不同敏感性。最大舒张率分别为未经处理的制剂的30-38%和13-17%,但消炎痛和环加氧酶抑制剂对反应无影响。受体拮抗剂阿托品,苯海拉明,[D-Pro(2),D-Trp(7、9)]-物质P或普萘洛尔均未对GS-ARMG诱导的松弛产生任何明显的抑制作用。但是,阿托品或普萘洛尔会导致松弛减少10%,这表明毒蕈碱受体或β-肾上腺素受体可能参与了GS-ARMG诱导的松弛。这些结果表明,GS-ARMG产生与GS-RG类似的内皮依赖性舒张大鼠主动脉。一氧化氮产生的增加和内皮细胞cGMP血管水平的增加可能有助于松弛。但是,GS-ARMG具有比GS-RG更强的活性,可通过一种或多种活性物质来放松离体的大鼠主动脉,由于山上的生长条件或制造GS-ARMG的过程,山参的含量可能更高。 ARMG。这些因素可能有助于理解山参的生物有益作用。

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