Inhibition of mast cell activation via MRGPRX2 receptor by Curcuma mangga and Sonchus arvensis water suspensions: An in vitro study.

IF 2.2 Q3 CHEMISTRY, MEDICINAL
Muhammad Novrizal Abdi Sahid, Masaki Mogi, Kazutaka Maeyama
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引用次数: 0

Abstract

Objective: Traditional medicine is often used to relief pain, but its use is frequently not supported by appropriate scientific information. This study aims to investigate the histamine release suppression of Sonchus arvensis (SA) and Curcuma mangga (CM).

Materials and methods: Rat peritoneal mast cells (RPMCs) and Mas-related GPCR-X2(MRGPRX2)-transfected RBL-2H3 cells were activated by 50 μg/ml of compound 48/80. Water suspension of SA or CM (0.1-30 mg/ml) was used to inhibit cell activation by compound 48/80. The level of mast cell activation was determined by measuring histamine release concentration using HPLC-fluorometry.

Results: At a concentration of 10 mg/ml, CM resulted in 22.60±5.86% in a spontaneous histamine release from RPMCs. The net histamine release after compound 48/80 stimulation in RPMC was 67.19±1.31%. CM at 3 mg/ml suppressed histamine release to 8.45±2.53%. In MRGPRX2-transfected RBL-2H3 cells stimulated with compound 48/80, CM at concentrations of 3 and 10 mg/mL suppressed histamine release to 22.85±0.64% and 4.20±1.60%, respectively. SA at 30 mg/ml induced a spontaneous histamine release of 56.76±4.03%, compared to 5.65±2.61% in the control group. The administration of 3 mg/ml of SA to compound 48/80-stimulated RPMCs resulted in a net histamine release of 6.12±0.46%. In MRGPRX2-transfected RBL-2H3 cells activated by compound 48/80, the net release was 35.11±3.10%. SA at 10 mg/ml suppressed histamine release to 4.88±1.42%.

Conclusion: SA and CM water suspension suppressed compound 48/80-induced histamine release.

Abstract Image

Abstract Image

姜黄和水混悬液通过MRGPRX2受体抑制肥大细胞活化的体外研究
目的:传统医学常用于缓解疼痛,但其使用往往没有适当的科学信息支持。本研究的目的是研究松果(Sonchus arvensis, SA)和姜黄(Curcuma mangga, CM)对组胺释放的抑制作用。材料与方法:用50 μg/ml化合物48/80激活大鼠腹膜肥大细胞(RPMCs)和转染mas相关GPCR-X2(MRGPRX2)的RBL-2H3细胞。采用SA或CM水悬浮液(0.1 ~ 30 mg/ml)抑制化合物48/80对细胞的活化作用。采用高效液相色谱-荧光法测定组胺释放浓度,测定肥大细胞活化水平。结果:CM浓度为10 mg/ml时,组胺自发性释放率为22.60±5.86%;复方48/80刺激后RPMC净组胺释放量为67.19±1.31%。CM浓度为3 mg/ml时,组胺释放抑制率为8.45±2.53%。化合物48/80刺激mrgprx2转染的RBL-2H3细胞,CM浓度为3和10 mg/mL时,组胺释放抑制率分别为22.85±0.64%和4.20±1.60%。30 mg/ml SA诱导组胺自发性释放率为56.76±4.03%,对照组为5.65±2.61%。3 mg/ml SA给药于48/80刺激的RPMCs,组胺净释放量为6.12±0.46%。经化合物48/80活化的mrgprx2转染的RBL-2H3细胞,净释放量为35.11±3.10%。10 mg/ml SA抑制组胺释放为4.88±1.42%。结论:SA和CM水悬浮液可抑制复方48/80诱导的组胺释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Avicenna Journal of Phytomedicine
Avicenna Journal of Phytomedicine CHEMISTRY, MEDICINAL-
CiteScore
3.40
自引率
4.50%
发文量
17
审稿时长
6 weeks
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