References
- Gregoire, F.M., Smas, C.M., Sul, H.S. Understanding adipocyte differentiation. Physiol Rev. 78(3):783-809, 1998. https://doi.org/10.1152/physrev.1998.78.3.783
- Trujillo, M.E., Scherer, P.E. Adipose tissue-derived factors: impact on health and disease. Endocr Rev. 27(7):762-778, 2006. https://doi.org/10.1210/er.2006-0033
- Fajas, L., Schoonjans, K., Gelman, L., Kim, J.B., Najib, J., Martin, G., Fruchart, J.C., Briggs, M., Spiegelman, B.M., Auwerx, J. Regulation of peroxisome proliferator-activated receptor gamma expression by adipocyte differentiation and determination factor 1/sterol regulatory element binding protein 1: implications for adipocyte differentiation and metabolism. Mol Cell Biol. 19(8):5495-5503, 1999. https://doi.org/10.1128/MCB.19.8.5495
- Kim, J.B., Spiegelman, B.M. ADD1/SREBP1 promotes adipocyte differentiation and gene expression linked to fatty acid metabolism. Genes Dev. 10(9):1096-1107, 1996. https://doi.org/10.1101/gad.10.9.1096
- Le Lay, S., Lefrere, I., Trautwein, C., Dugail, I., Krief, S. Insulin and sterol-regulatory element-binding protein-1c (SREBP-1C) regulation of gene expression in 3T3-L1 adipocytes. Identification of CCAAT/enhancer-binding protein beta as an SREBP-1C target. J Biol Chem. 277(38):35625-35634, 2002. https://doi.org/10.1074/jbc.M203913200
- Roh, S.W., Kim, J.B. Effects of Polygonati Rhizoma on the Diet-induced Hyperlipidemia in Rats. Korean J Oriental Physiology & Pathology. 22(5):1147-1151, 2008.
- Lin, J., Della-Fera, M.A., Baile, C.A. Green tea polyphenol epigallocatechin gallate inhibits adipogenesis and induces apoptosis in 3T3-L1 adipocytes. Obes Res 13(6):982-990, 2005. https://doi.org/10.1038/oby.2005.115
- Hassan, M., El Yazidi, C., Landrier, J.F., Lairon, D., Margotat, A., Amiot, M.J. Phloretin enhances adipocyte differentiation and adiponectin expression in 3T3-L1 cells. Biochem Biophys Res Commun 361(1):208-213, 2007. https://doi.org/10.1016/j.bbrc.2007.07.021
- 李尙仁. 本草學. 서울, 醫藥社, pp 394-395, 1983.
- Bang, J.S., Oh, D.H., Choi, H.M., Sur, B.J., Lim, S.J., Kim, J.Y., Yang, H.I., Yoo, M.C., Hahm, D.H., Kim, K.S. Anti-inflammatory and antiarthritic effects of piperine in human interleukin 1beta-stimulated fibroblast-like synoviocytes and in rat arthritis models. Arthritis Res Ther. 11(2):R49, 2009. https://doi.org/10.1186/ar2662
- Vijayakumar, R.S., Nalini, N. Efficacy of piperine, an alkaloidal constituent from Piper nigrum on erythrocyte antioxidant status in high fat diet and antithyroid drug induced hyperlipidemic rats. Cell Biochem Funct 24(6):491-498, 2006. https://doi.org/10.1002/cbf.1331
- Bajad, S., Bedi, K.L., Singla, A.K., Johri, R.K. Antidiarrhoeal activity of piperine in mice. Planta Med. 67(3):284-287, 2001. https://doi.org/10.1055/s-2001-11999
- Szallasi, A. Piperine: researchers discover new flavor in an ancient spice. Trends Pharmacol Sci. 26(9):437-439, 2005.
- Jeong, H.S., Jeong, J.C. Anti-adipogencic Effect of Piper Nigrum Linne. Korean Journal of Oriental Physiology and Pathology. 24(1):118-123, 2010.
- Parmar, V.S., Jain, S.C., Bisht, K.S., Jain, R., Taneja, P., Jha, A., Tyagi, O.D., Prasad, A.K., Wengel, J., Olsen, C.E. Phytochemistry of the genus Piper. Phytochemistry. 46(4):597-673, 1997. https://doi.org/10.1016/S0031-9422(97)00328-2
- Kaleem, M., Sheema Sarmad, H., Bano, B. Protective effects of Piper nigrum and Vinca rosea in alloxan induced diabetic rats. Indian J Physiol Pharmacol. 49(1):65-71, 2005.
- Jin, Z., Borjihan, G., Zhao, R., Sun, Z., Hammond, G.B., Uryu, T. Antihyperlipidemic compounds from the fruit of Piper longum L. Phytother Res. 23(8):1194-1196, 2009. https://doi.org/10.1002/ptr.2630
- Lee, S.W., Rho, M.C., Park, H.R., Choi, J.H., Kang, J.Y., Lee, J.W., Kim, K., Lee, H.S., Kim, Y.K. Inhibition of diacylglycerol acyltransferase by alkamides isolated from the fruits of Piper longum and Piper nigrum. J Agric Food Chem. 54(26):9759-9763, 2006. https://doi.org/10.1021/jf061402e
- Sunila, E.S., Kuttan, G. Immunomodulatory and antitumor activity of Piper longum Linn. and piperine. J Ethnopharmacol. 90(2-3):339-346, 2004. https://doi.org/10.1016/j.jep.2003.10.016
- Faas, L., Venkatasamy, R., Hider, R.C., Young, A.R., Soumyanath, A. In vivo evaluation of piperine and synthetic analogues as potential treatments for vitiligo using a sparsely pigmented mouse model. Br J Dermatol. 158(5):941-950, 2008. https://doi.org/10.1111/j.1365-2133.2008.08464.x
- Hamm, J.K., el Jack, A.K., Pilch, P.F., Farmer, S.R. Role of PPAR gamma in regulating adipocyte differentiation and insulin-responsive glucose uptake. Ann N Y Acad Sci. 892: 134-145, 1999. https://doi.org/10.1111/j.1749-6632.1999.tb07792.x
- Juvet, L.K., Andresen, S.M., Schuster, G.U., Dalen, K.T., Tobin, K.A., Hollung, K, Haugen, F, Jacinto, S, Ulven, S.M., Bamberg, K. On the role of liver X receptors in lipid accumulation in adipocytes. Mol Endocrinol 17(2):172-182, 2003. https://doi.org/10.1210/me.2001-0210
- Schoonjans, K., Gelman, L., Haby, C., Briggs, M., Auwerx, J. Induction of LPL gene expression by sterols is mediated by a sterol regulatory element and is independent of the presence of multiple E boxes. J Mol Biol. 304(3):323-334, 2000. https://doi.org/10.1006/jmbi.2000.4218
- Shimomura, I., Hammer, R.E., Richardson, J.A., Ikemoto, S., Bashmakov, Y., Goldstein, J.L., Brown, M.S. Insulin resistance and diabetes mellitus in transgenic mice expressing nuclear SREBP-1c in adipose tissue: model for congenital generalized lipodystrophy. Genes Dev. 12(20):3182-3194, 1998. https://doi.org/10.1101/gad.12.20.3182
- Zhang, L.L., Yan Liu, D., Ma, L.Q., Luo, Z.D., Cao, T.B., Zhong, J., Yan, Z.C., Wang, L.J., Zhao, Z.G., Zhu, S.J. Activation of transient receptor potential vanilloid type-1 channel prevents adipogenesis and obesity. Circ Res. 100(7):1063-1070, 2007. https://doi.org/10.1161/01.RES.0000262653.84850.8b