Background: The management of acute inflammation, which arises from complex biological responses to harmful stimuli, is an important determinant in the recovery from an otherwise detrimental outcome such as septicemia. However, the side effects and limitations of current therapeutics necessitate the development of newer and safer alternatives. Mollugo cerviana is a common medicinal herb of the Indian subcontinent and has been traditionally used for its fever mitigating anti-microbial and hepatoprotective action. We have already reported the rich presence of radical scavenging phytochemicals in the plant extracts and their strong antioxidant properties. Objective: In the present study, we have evaluated the anti-inflammatory effects of methanolic extract (ME) of the areal parts of M. cerviana in a lipopolysaccharide (LPS)-induced acute inflammatory cell culture model. Methods: RAW 264.7 mouse macrophage cells were stimulated by the bacterial endotoxin LPS at a concentration of 1 mu g/mL. Cytotoxicity and anti-inflammatory potential of ME were carried out. Results: The concentration of M. cerviana extract up to 150 mu g/ml was found to be non-toxic to cells (MTT and NRU assay). LPS induces acute inflammation by binding to TLR-4 receptors, initiating a downstream signalling cascade that results in pro-inflammatory cytokine secretion. Extract treatment at 100 mu g/ml suppressed LPS-induced gene expression (qPCR) and secretion (ELISA) of pro-inflammatory cytokines IL-1 beta, IL-6 and TNF-alpha, and the chemokine CCL2, leading to dampening of the acute inflammatory cascade. LPS-induced elevation of ROS level (DCFDA method) was significantly reduced by extract treatment. Nitric oxide production, as indicated by nitrite level, was significantly reduced post extract treatment. Conclusion: This study demonstrated that M. cerviana methanolic extract has a potent anti-inflammatory effect in the in vitro acute inflammation model of LPS-stimulated RAW 264.7 cells. There is no reported study so far on the anti-inflammatory properties of M. cerviana in an LPS-induced acute inflammatory model, which closely mimics a human bacteremia response. Hence, this study highlights the therapeutic potential of this extract as a source of anti-inflammatory lead molecules.
机构:
Daegu Univ, Grad Sch, Dept Rehabil Sci, Gyongsan 712714, Kyeongbuk, South KoreaDaegu Univ, Grad Sch, Dept Rehabil Sci, Gyongsan 712714, Kyeongbuk, South Korea
Seo, Seong-Wook
Kim, Kyoung
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Daegu Univ, Coll Rehabil Sci, Dept Phys Therapy, Gyeongbuk 712714, South Korea
Daegu Univ, Coll Rehabil Sci, Dept Phys Therapy, Gyeongsangbugdo 38453, South KoreaDaegu Univ, Grad Sch, Dept Rehabil Sci, Gyongsan 712714, Kyeongbuk, South Korea
机构:
Univ Tsukuba, Grad Sch Life & Environm Sci, Tennodai 1-1-1, Tsukuba, Ibaraki 3058572, JapanUniv Tsukuba, Grad Sch Life & Environm Sci, Tennodai 1-1-1, Tsukuba, Ibaraki 3058572, Japan
Tian, Yuan
Zhou, Siqi
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Univ Tsukuba, Grad Sch Life & Environm Sci, Tennodai 1-1-1, Tsukuba, Ibaraki 3058572, JapanUniv Tsukuba, Grad Sch Life & Environm Sci, Tennodai 1-1-1, Tsukuba, Ibaraki 3058572, Japan
Zhou, Siqi
Takeda, Reiko
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Univ Tsukuba, Grad Sch Life & Environm Sci, Tennodai 1-1-1, Tsukuba, Ibaraki 3058572, Japan
Kohaku Bio Technol Co Ltd, Tsukuba, Ibaraki 3058572, JapanUniv Tsukuba, Grad Sch Life & Environm Sci, Tennodai 1-1-1, Tsukuba, Ibaraki 3058572, Japan
Takeda, Reiko
Okazaki, Kazuma
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Kohaku Bio Technol Co Ltd, Tsukuba, Ibaraki 3058572, JapanUniv Tsukuba, Grad Sch Life & Environm Sci, Tennodai 1-1-1, Tsukuba, Ibaraki 3058572, Japan
Okazaki, Kazuma
Sekita, Marie
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Kohaku Bio Technol Co Ltd, Tsukuba, Ibaraki 3058572, JapanUniv Tsukuba, Grad Sch Life & Environm Sci, Tennodai 1-1-1, Tsukuba, Ibaraki 3058572, Japan
Sekita, Marie
Sakamoto, Kazuichi
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Univ Tsukuba, Grad Sch Life & Environm Sci, Tennodai 1-1-1, Tsukuba, Ibaraki 3058572, JapanUniv Tsukuba, Grad Sch Life & Environm Sci, Tennodai 1-1-1, Tsukuba, Ibaraki 3058572, Japan
机构:
Seoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
Shin, E. M.
Zhou, H. Y.
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Seoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
Shenyang Pharmaceut Univ, Coll Pharm, Dept Pharmacol, Shenyang 110016, Peoples R ChinaSeoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
Zhou, H. Y.
Guo, L. Y.
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Seoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
Guo, L. Y.
Kong, S. S.
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Seoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
Kong, S. S.
Kim, J. A.
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Yeungnam Univ, Coll Pharm, Gyongsan 712749, South KoreaSeoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
Kim, J. A.
Lee, S. H.
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Yeungnam Univ, Coll Pharm, Gyongsan 712749, South KoreaSeoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
Lee, S. H.
Merfort, I
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Univ Freiburg, Dept Pharmaceut Biol & Biotechnol, D-79104 Freiburg, GermanySeoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
Merfort, I
Kim, H. S.
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Wonkwang Univ, Coll Pharm, Iksan 570749, South KoreaSeoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
Kim, H. S.
Kim, S.
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Seoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
Kim, S.
Kim, Y. S.
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Seoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea