Anti-inflammatory Activity Guided Fractionation of Aerial Parts of Clematis gouriana Roxb. ex DC

References

• Simmons, D.L. (2006). What makes a good anti-inflammatory drug target? Drug Discov. Today. 11: 210-219. doi: 10.1016/S1359-6446(05)03721-9
   PubMed Web of Science ®Google Scholar
• Pahwa, R., Goyal, A., Jialal, I. (2021). Chronic inflammation. StatPearls [Internet].
   Google Scholar
• Arulselvan, P., Fard, M.T., Tan, W.S., Gothai, S., Fakurazi, S., Norhaizan, M.E., Kumar, S. S. (2016). Role of antioxidants and natural products in inflammation. Oxid. Med. Cell. Longev. 2016. doi: 10.1155/2016/5276130
   PubMed Web of Science ®Google Scholar
• Pahlavani, N., Malekahmadi, M., Firouzi, S., Rostami, D., Sedaghat, A., Moghaddam, A.B., Ferns, G.A., Navashenaq, J.G., Reazvani, R., Safarian, M. (2020). Molecular and cellular mechanisms of the effects of Propolis in inflammation, oxidative stress and glycemic control in chronic diseases. Nutrition & Metabolism. 17: 1-12. doi: 10.1186/s12986-019-0425-9
   PubMed Web of Science ®Google Scholar
• Alagarsamy, V., Meena, S., Ramseshu, K., Solomon, V., Thirumurugan, K., Dhanabal, K., Murugan, M. (2006). Synthesis, analgesic, anti-inflammatory, ulcerogenic index and antibacterial activities of novel 2-methylthio-3-substituted-5, 6, 7, 8-tetrahydrobenzo (b) thieno [2, 3-d] pyrimidin-4 (3H)-ones. Eur. J. Med. Chem. 41: 1293-1300. doi: 10.1016/j.ejmech.2006.06.005
   PubMed Web of Science ®Google Scholar
• Arulselvan, P., Fard, M.T., Tan, W.S., Gothai, S., Fakurazi, S., Norhaizan, ME., Kumar, S.S. (2016). Role of Antioxidants and Natural Products in Inflammation. Oxid. Med. Cell. Longev. 2016. doi: 10.1155/2016/5276130
   PubMed Web of Science ®Google Scholar
• Organization, W.H. (2016). WHO global report on traditional and complementary medicine. World Health Organization. 2019.
   Google Scholar
• Sychrová, A., Koláriková, I., Žemlička, M., Šmejkal, K. (2020). Natural compounds with dual antimicrobial and anti-inflammatory effects. Phytochem Rev. 19: 1471-1502. doi: 10.1007/s11101-020-09694-5
   Web of Science ®Google Scholar
• Nattagh-Eshtivani, E., Barghchi, H., Pahlavani, N., Barati, M., Amiri, Y., Fadel, A., Khosravi, M., Talebi, S., Arzhang, P., Ziaei, R., Ghavami, A. (2022). Biological and pharmacological effects and nutritional impact of phytosterols: A comprehensive review. Phytother. Res. 36: 299-322. doi: 10.1002/ptr.7312
   PubMed Web of Science ®Google Scholar
• Hadi, V., Pahlavani, N., Malekahmadi, M., Nattagh-Eshtivani, E., Navashenaq, J.G., Hadi, S., Ferns, G.A., Ghayour-Mobarhan, M., Askari, G., Norouzy, A. (2021). Nigella sativa in controlling Type 2 diabetes, cardiovascular, and rheumatoid arthritis diseases: Molecular aspects. J. Res. Med. Sci 26.
   PubMed Web of Science ®Google Scholar
• Shabgah, A.G., Zarifi, S.H., Kiapey, S.S.M., Ezzatifar, F., Pahlavani, N., Soleimani, D., Haftcheshmeh, S.M., Mohammadi, H., Navashenaq, J.G. (2021). Curcumin and cancer; are long non-coding RNAs missing link? Prog. Biophy. Mol. Bio. 164: 63-71. doi: 10.1016/j.pbiomolbio.2021.04.001
   PubMed Web of Science ®Google Scholar
• Rohdewald, P.J. (2018). Review on sustained relief of osteoarthritis symptoms with a proprietary extract from pine bark, Pycnogenol J. Med. Food. 21: 1-4. doi: 10.1089/jmf.2017.0015
   PubMed Web of Science ®Google Scholar
• Yuan, L., Zhang, F., Shen, M., Jia, S., Xie, J. (2019). Phytosterols suppress phagocytosis and inhibit inflammatory mediators via ERK pathway on LPS-triggered inflammatory responses in RAW264. 7 macrophages and the correlation with their structure. Foods. 8: 582. doi: 10.3390/foods8110582
   PubMed Web of Science ®Google Scholar
• Hamdy, N.M., Taha, R. A.( 2009). Effects of Nigella sativa oil and thymoquinone on oxidative stress and neuropathy in streptozotocin-induced diabetic rats. Pharmacology. 84: 127-134. doi: 10.1159/000234466
   PubMed Web of Science ®Google Scholar
• Pahlavani, N., Sedaghat, A., Moghaddam, A.B., Kiapey, S.S.M., Navashenaq, J.G., Jarahi, L., Reazvani, R., Norouzy, A., Nematy, M., Safarian, M. (2019). Effects of propolis and melatonin on oxidative stress, inflammation, and clinical status in patients with primary sepsis: Study protocol and review on previous studies. Clin. Nutr. ESPEN. 33: 125-131. doi: 10.1016/j.clnesp.2019.06.007
   PubMed Web of Science ®Google Scholar
• Oh, Y., Kwon, Y.-S., Jung, B.D. (2017). Anti-inflammatory effects of the natural compounds cortex phellodendri and humulus japonicus on pelvic inflammatory disease in mice. International Journal of Medical Sciences. 14: 729. doi: 10.7150/ijms.19616
   PubMed Web of Science ®Google Scholar
• Malekahmadi, M., Moradi Moghaddam, O., Islam, S.M.S., Tanha, K., Nematy, M., Pahlavani, N., Firouzi, S., Zali, M.R., Norouzy, A. (2020). Evaluation of the effects of pycnogenol (French maritime pine bark extract) supplementation on inflammatory biomarkers and nutritional and clinical status in traumatic brain injury patients in an intensive care unit: A randomized clinical trial protocol. Trials. 21: 1-9. doi: 10.1186/s13063-019-4008-x
   PubMed Web of Science ®Google Scholar
• Chen, R., Cui, L., Guo, Y., Rong, Y., Lu, X., Sun, M., Zhang, L., Tian, J. (2011). In vivo study of four preparative extracts of Clematis terniflora DC. for antinociceptive activity and anti-inflammatory activity in rat model of carrageenan-induced chronic non-bacterial prostatitis. J. Ethnopharmacol. 134: 1018-1023. doi: 10.1016/j.jep.2011.01.004
   PubMed Web of Science ®Google Scholar
• Chawla, R., Kumar, S., Sharma, A. (2012). The genus Clematis (Ranunculaceae): Chemical and pharmacological perspectives. J. Ethnopharmacol. 143: 116-150. doi: 10.1016/j.jep.2012.06.014
   PubMed Web of Science ®Google Scholar
• Sharma, S., Chunekar, K. (1998). Medicinal plants used in Ayurveda. Rashtriya Ayurveda Vidyapeeta, New Delhi.
   Google Scholar
• Quattrocchi, U. (2012). CRC world dictionary of medicinal and poisonous plants: common names, scientific names, eponyms, synonyms, and etymology (5 Volume Set). CRC press:.
   Google Scholar
• Sandhyarani, G., Ramesh, A., Naik, B. (2014). Study on ethno-medico-botany of some plants of Tirupati district of Andhra Pradesh, India. J. Altern. Complement Med. 1: 35-37.
   Google Scholar
• Rana, S., Rawat, K., Mahendru, M., Padwad, Y., Pakade, Y.B., Lal, B., Bhushan, S. (2015). Screening of bioconstituents and in vitro cytotoxicity of Clematis gouriana leaves. Nat. Prod. Res. 29: 2242-2246. doi: 10.1080/14786419.2014.1000891
   PubMed Web of Science ®Google Scholar
• Karimi, E., Ghorbani Nohooji, M., Habibi, M., Ebrahimi, M., Mehrafarin, A., Khalighi-Sigaroodi, F. (2018). Antioxidant potential assessment of phenolic and flavonoid rich fractions of Clematis orientalis and Clematis ispahanica (Ranunculaceae). Nat. Prod. Res. 32: 1991-1995. doi: 10.1080/14786419.2017.1359171
   PubMed Web of Science ®Google Scholar
• Wang, L., Wang, P., Wang, D., Tao, M., Xu, W., Olatunji, O.J. (2020). Anti-inflammatory activities of kukoamine A from the root bark of Lycium chinense miller. Nat. Prod. Commun. 15: 1934578X20912088.
   PubMed Web of Science ®Google Scholar
• Hu, C., Zawistowski, J., Ling, W., Kitts, D.D. (2003). Black rice (Oryza sativa L. indica) pigmented fraction suppresses both reactive oxygen species and nitric oxide in chemical and biological model systems. J. Agric. Food Chem. 51: 5271-5277. doi: 10.1021/jf034466n
   PubMed Web of Science ®Google Scholar
• Jachak, S.M., Gautam, R., Selvam, C., Madhan, H., Srivastava, A., Khan, T. (2011). Anti-inflammatory, cyclooxygenase inhibitory and antioxidant activities of standardized extracts of Tridax procumbens L. Fitoterapia. 82: 173-177. doi: 10.1016/j.fitote.2010.08.016
   PubMed Web of Science ®Google Scholar
• Wang, Y., Zheng, M., Jiang, Q., Xu, Y., Zhou, X., Zhang, N., Sun, D., Li, H., Chen, L. (2021). Chemical Components of the Fruits of Morus nigra Linn.: Methyl Caffeate as a Potential Anticancer Agent by Targeting 3-Phosphoglycerate Dehydrogenase J. Agric. Food Chem. 69: 12433-12444. doi: 10.1021/acs.jafc.1c03215
   PubMed Web of Science ®Google Scholar
• Lu, Y., Foo, L.Y. (1997). Identification and quantification of major polyphenols in apple pomace. Food chem. 59: 187-194. doi: 10.1016/S0308-8146(96)00287-7
   Web of Science ®Google Scholar
• Lin, H.-Y., Kuo, Y.-H., Lin, Y.-L., Chiang, W. (2009). Antioxidative effect and active components from leaves of Lotus (Nelumbo nucifera). J. Agric. Food Chem. 57: 6623-6629. doi: 10.1021/jf900950z
   PubMed Web of Science ®Google Scholar
• Li, Z.-H., Guo, H., Xu, W.-B., Ge, J., Li, X., Alimu, M., He, D.-J. (2016). Rapid identification of flavonoid constituents directly from PTP1B inhibitive extract of raspberry (Rubus idaeus L.) leaves by HPLC–ESI–QTOF–MS-MS. J. Chromatogr. Sci. 54: 805-810. doi: 10.1093/chromsci/bmw016
   PubMed Web of Science ®Google Scholar
• Rho, T., Yoon, K.D. (2017). Chemical constituents of Nelumbo nucifera seeds. Nat. Prod. Sci. 23: 253-257. doi: 10.20307/nps.2017.23.4.253
   Google Scholar
• Búfalo, M.C., Ferreira, I., Costa, G., Francisco, V., Liberal, J., Cruz, M.T., Lopes, M.C., Batista, M.T., Sforcin, J.M. (2013). Propolis and its constituent caffeic acid suppress LPS-stimulated pro-inflammatory response by blocking NF-κB and MAPK activation in macrophages. J. Ethnopharmacol. 149: 84-92. doi: 10.1016/j.jep.2013.06.004
   PubMed Web of Science ®Google Scholar
• Shin, K.-M., Kim, I.-T., Park, Y.-M., Ha, J., Choi, J.-W., Park, H.-J., Lee, Y.S., Lee, K.-T. (2004). Anti-inflammatory effect of caffeic acid methyl ester and its mode of action through the inhibition of prostaglandin E2, nitric oxide and tumor necrosis factor-α production. Biochem. Pharmaco. 68: 2327-2336. doi: 10.1016/j.bcp.2004.08.002
   PubMed Web of Science ®Google Scholar
• Kang, K.S., Yokozawa, T., Kim, H.Y., Park, J.H. (2006). Study on the nitric oxide scavenging effects of ginseng and its compounds. J. Agric. Food Chem. 54: 2558-2562. doi: 10.1021/jf0529520
   PubMed Web of Science ®Google Scholar
• Lee, S., Park, H.S., Notsu, Y., Ban, H.S., Kim, Y.P., Ishihara, K., Hirasawa, N., Jung, S.H., Lee, Y.S., Lim, S.S. (2008). Effects of hyperin, isoquercitrin and quercetin on lipopolysaccharide-induced nitrite production in rat peritoneal macrophages. Phytother. Res. 22: 1552-1556. doi: 10.1002/ptr.2529
   PubMed Web of Science ®Google Scholar