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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.
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页码:204 / 210
页数:7
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