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      Chemical Constituents from the Roots and Rhizomes of Asarum heterotropoides var. mandshuricum and the In Vitro Anti-Inflammatory Activity

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          Abstract

          Anti-inflammatory compounds were investigated from the ethanol extract of the roots and rhizomes of Asarum heterotropoides var. mandshuricum, a traditional Chinese medicine called Xixin and used for pain and inflammatory. Nine new compounds were isolated, including six new lignans, neoasarinin A–C ( 13), neoasarininoside A and B ( 4 and 5), and asarinin B ( 7), and one new monoterpene, asarincin A ( 8), two new amides, asaramid II and III ( 10 and 11), and one new natural monoterpene, asaricin B ( 9), along with 37 known compounds ( 6, 1247). Their structures and absolute configurations were elucidated on the basis of spectroscopic methods and chemical analyses. This is the first report of the absolute configuration of asarinin A ( 6). The 8- O-4′ neolignans ( 15) were reported in the genus Asarum for the first time. The 15 compounds 17, 19, 2225, 28, 31, 36, 40, 42, 43, 4547 were isolated from the genus Asarum, and compounds 16, 32, 33, 37 and 39 were isolated from A. heterotropoides var. mandshuricum for the first time. Thirty-seven of the isolates were evaluated for anti-inflammatory activity against the release of β-glucuronidase in polymorphonuclear leukocytes (PMNs) induced by the platelet-activating factor (PAF), and compounds 1, 4, 7, 8, 14, 1719, 22, 24, 25, 29, 30, 32, 33, 4043, 45, and 46 showed potent anti-inflammatory activities in vitro, with 27.9%–72.6% inhibitions at 10 −5 mol/L. The results of anti-inflammatory assay suggested that lignans obtained from the CHCl 3 extract might be the main active components of Xixin.

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          Protective effect of naringenin in experimental ischemic stroke: down-regulated NOD2, RIP2, NF-κB, MMP-9 and up-regulated claudin-5 expression.

          Inflammatory damage plays a pivotal, mainly detrimental role in cerebral ischemic pathogenesis and may represent a promising target for treatment. Naringenin (NG) has gained growing appreciation for its beneficial biological effects through its anti-inflammatory property. Whether this protective effect applies to cerebral ischemic injury, we therefore investigate the potential neuroprotective role of NG and the underlying mechanisms. Focal cerebral ischemia in male Sprague-Dawley rats was induced by permanent middle cerebral artery occlusion (pMCAO) and NG was pre-administered intragastrically once daily for four consecutive days before surgery. Neurological deficit, brain water content and infarct volume were measured at 24 h after stroke. Immunohistochemistry, Western blot and RT-qPCR were used to explore the anti-inflammatory potential of NG in the regulation of NOD2, RIP2 and NF-κB in ischemic cerebral cortex. Additionally, the activities of MMP-9 and claudin-5 were analyzed to detect NG's influence on blood-brain barrier. Compared with pMCAO and Vehicle groups, NG noticeably improved neurological deficit, decreased infarct volume and edema at 24 h after ischemic insult. Consistent with these results, our data also indicated that NG significantly downregulated the expression of NOD2, RIP2, NF-κB and MMP-9, and upregulated the expression of claudin-5 (P < 0.05). The results provided a neuroprotective profile of NG in cerebral ischemia, this effect was likely exerted by down-regulated NOD2, RIP2, NF-κB, MMP-9 and up-regulated claudin-5 expression.
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            Biosynthesis of antioxidant lignans in Sesamum indicum seeds

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              Anti-inflammatory and PPAR transactivational effects of secondary metabolites from the roots of Asarum sieboldii.

              Phytochemical study on the roots of Asarum sieboldii resulted in the isolation of one new compound, (1R,2S,5R,6R)-5'-O-methylpluviatilol (1) and 12 known compounds (2-13). Their structures were determined by extensive spectroscopic methods, including 1D and 2D NMR, and MS spectra. The absolute configuration of compound 1 was established using CD spectrum. Compounds 4, 5, and 12/13 significantly inhibited TNFα-induced NF-κB transcriptional activity in HepG2 cells in a dose-dependent manner, with IC(50) values ranging from 6.4 to 9.4 μM. Furthermore, the transcriptional inhibitory function of these compounds was confirmed based on decreases in COX-2 and iNOS gene expression in HepG2 cells. Compounds 1-3, 6,7, 10, and 11 significantly activated the transcriptional activity of PPARs in a dose-dependent manner, with EC(50) values ranging from 1.7 to 20.9 μM. Compounds 7, 10, and 11 exhibited significant dose-dependent PPARα transactivational activity, with EC(50) values of 19.5, 15.7, and 4.0 μM, respectively. Compounds 1, 6, 7, 10, and 11 activated PPARγ transcriptional activity, with EC(50) values ranging from 3.6 to 22.6 μM, whereas compounds 10 and 11 significantly increased PPARβ(δ) transactivational activity, with EC(50) values of 22.6 and 4.9 μM, respectively. These results provide a scientific support for the use of the roots of A. sieboldii and warrant further studies to develop new agents for the prevention and treatment of the inflammatory and metabolic diseases.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Molecules
                Molecules
                molecules
                Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
                MDPI
                1420-3049
                13 January 2017
                January 2017
                : 22
                : 1
                : 125
                Affiliations
                [1 ]State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University Health Science Center, No. 38, Xueyuan Road, Beijing 100191, China; jing_jy@ 123456126.com (Y.J.); zhangyifan@ 123456bjmu.edu.cn (Y.-F.Z.); guangxl@ 123456bjmu.edu.cn (G.-X.L.); 13466759800@ 123456163.com (Y.-L.L.); xuanwang6818@ 123456bjmu.edu.cn (X.W.)
                [2 ]Tonghua Gold-Horse Pharmaceutical Group Co., Ltd., Beijing 100025, China
                Author notes
                [* ]Correspondence: myshang@ 123456bjmu.edu.cn (M.-Y.S.); sqcai@ 123456bjmu.edu.cn (S.-Q.C.); Tel./Fax: +86-10-8280-2534 (M.-Y.S.); +86-10-8280-1693 (S.-Q.C.)
                Article
                molecules-22-00125
                10.3390/molecules22010125
                6155747
                28098805
                8c2f6740-ecad-4417-91f6-90be0962d894
                © 2017 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 14 December 2016
                : 06 January 2017
                Categories
                Article

                asarum heterotropoides var. mandshuricum,aristolochiaceae,lignans,8-o-4′ neolignan,amide,monoterpene,anti-inflammatory

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