Assessment of Anti-inflammatory Activity of 3-Acetylmyricadiol in LPS-Stimulated Raw 264.7 Macrophages

被引:14
作者
Ahmad, Gazanfar [1 ]
Hassan, Reyaz [2 ]
Dhiman, Neerupma [1 ]
Ali, Asif [3 ,4 ]
机构
[1] Amity Univ, Amity Inst Pharm, Noida 201301, Uttar Pradesh, India
[2] Univ Kashmir, Dept Pharmaceut Sci, Srinagar 190006, India
[3] CSIR Indian Inst Integrat Med, Canal Rd, Jammu 180001, India
[4] CSIR Tradit Knowledge Digital Lib TKDL, 14 Satsang Vihar, New Delhi 110067, India
关键词
3-Acetylmyricadiol; inflammation; nitric oxide; IL-6; TNF-alpha; raw; 264.7; macrophages; NITRIC-OXIDE; INFLAMMATION; DRUGS; CELLS; CYTOKINES; LEAVES; ROLES;
D O I
10.2174/1386207324666210319122650
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Pentacyclic triterpenoids are a biologically active class of phytoconstituents with diverse pharmacological activities, including anti-inflammatory action. Objective: In the current study, we isolated 3-Acetylmyricadiol, a pentacyclic triterpenoid, from the ethyl acetate bark extract of Myrica esculenta and evaluated it for anti-inflammatory potential. Methods: The ethyl acetate bark extract of the M. esculenta was subjected to column chromatography to isolate 3-Acetylmyricadiol. MTT assay was performed to check cell viability. The production of proinflammatory mediators like nitric oxide, IL-6, TNF-alpha were observed after the administration of 5, 10, 20 mu M of 3-Acetylmyricadiol in LPS-activated raw 246.7 macrophages by the reported methods. Results: MTT assay indicated more than 90% cell viability up to 20 mu M of 3-Acetylmyricadiol. The administration of 3-Acetylmyricadiol inhibited the production of nitric oxide, IL-6, TNF-alpha in a dose-dependent manner significantly in comparison to LPS treated cells. The maximum effect was observed at 20 mu M of 3-Acetylmyricadiol which resulted in 52.37, 63.10, and 55.37 % inhibition of nitric oxide, IL-6, and TNF-alpha, respectively. Conclusion: Our study demonstrated the anti-inflammatory action of 3-Acetylmyricadiol and can serve as a potential candidate in the development of the clinically efficient anti-inflammatory molecule.
引用
收藏
页码:204 / 210
页数:7
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