Fig. 1. Effect of proanthocyanidins on cell viability in RAW264.7 macrophages.
Fig. 2. Proanthocyanidins induced HO-1 protein expression.
Fig. 3. Proanthocyanidins significantly reduced LPS-induced NO production and iNOS expression.
Fig. 4. Proanthocyanidins treatment shown significant inhibitory effect on proinflammatory cytokines.
참고문헌
- Ammar el, S. M., Said, S. A., El-Damarawy, S. L. and Suddek, G. M. 2013. Cardioprotective effect of grape-seed proanthocyanidins on doxorubicin-induced cardiac toxicity in rats. Pharm. Biol. 51, 339-344. https://doi.org/10.3109/13880209.2012.729065
- Bagchi, D., Bagchi, M., Stohs, S. J., Das, D. K., Ray, S. D., Kuszynski, C. A., Joshi, S. S. and Pruess, H. G. 2000. Free radicals and grape seed proanthocyanidin extract: importance in human health and disease prevention. Toxicology 148, 187-197. https://doi.org/10.1016/S0300-483X(00)00210-9
- Bagchi, D., Garg, A., Krohn, R. L., Bagchi, M., Tran, M. X. and Stohs, S. J. 1997. Oxygen free radical scavenging abilities of vitamins C and E, and a grape seed proanthocyanidin extract in vitro. Res. Commun. Mol. Pathol. Pharmacol. 95, 179-189.
- Braune, J., Weyer, U., Hobusch, C., Mauer, J., Bruning, J. C., Bechmann, I. and Gericke, M. 2017. IL-6 Regulates M2 Polarization and local proliferation of adipose tissue macrophages in obesity. J. Immunol. 198, 2927-2934. https://doi.org/10.4049/jimmunol.1600476
-
De Simone, V., Franze, E., Ronchetti, G., Colantoni, A., Fantini, M. C., Di Fusco, D., Sica, G. S., Sileri, P., Mac Donald, T. T., Pallone, F., Monteleone, G. and Stolfi, C. 2015. Th17-type cytokines, IL-6 and TNF-
${\alpha}$ synergistically activate STAT3 and NF-${\kappa}B$ to promote colorectal cancer cell growth. Oncogene 34, 3493-503. https://doi.org/10.1038/onc.2014.286 - Dennery, P. A. 2014. Signaling function of heme oxygenase proteins. Antioxid. Redox. Signal. 20, 1743-1753. https://doi.org/10.1089/ars.2013.5674
-
El-Shitany, N. A. and Eid, B. 2017. Proanthocyanidin protects against cisplatin-induced oxidative liver damage through inhibition of inflammation and NF-
${\kappa}B$ /TLR-4 pathway. Environ. Toxicol. 32, 1952-1963. https://doi.org/10.1002/tox.22418 - He, L., Li, P., Yu, L. H., Li, L., Zhang, Y., Guo, Y., Long, M., He, J. B. and Yang, S. H. 2018. Protective effects of proanthocyanidins against cadmium-induced testicular injury through the modification of Nrf2-Keap1 signal path in rats. Environ. Toxicol. Pharmacol. 57, 1-8. https://doi.org/10.1016/j.etap.2017.11.002
- Lee, T. S. and Chau, L. Y. 2002. Heme oxygenase-1 mediates the anti-inflammatory effect of interleukin-10 in mice, Nat. Med. 8, 240-246. https://doi.org/10.1038/nm0302-240
- Lind, M., Hayes, A., Caprnda, M., Petrovic, D., Rodrigo, L., Kruzliak, P. and Zulli, A. 2017. Inducible nitric oxide synthase: Good or bad? Biomed. Pharmacother. 93, 370-375. https://doi.org/10.1016/j.biopha.2017.06.036
- Long, M., Yang, S., Zhang, Y., Li, P., Han, J., Dong, S., Chen, X. and He, J. 2017. Proanthocyanidin protects against acute zearalenone-induced testicular oxidative damage in male mice. Environ. Sci. Pollut. Res. Int. 24, 938-946. https://doi.org/10.1007/s11356-016-7886-4
- Matzneller, P., Strommer, S., Drucker, C., Petroczi, K., Schorgenhofer, C., Lackner, E., Jilma, B. and Zeitlinger, M. 2017. Colistin reduces LPS-triggered inflammation in a human sepsis model in vivo: A randomized controlled trial. Clin. Pharmacol. Ther. 101, 773-781. https://doi.org/10.1002/cpt.582
- Morse, D., Pischke, S. E., Zhou, Z., Davis, R. J., Flavell, R. A., Loop, T., Otterbein, S. L., Otterbein, L. E. and Choi, A. M. 2003. Suppression of inflammatory cytokine production by carbon monoxide involves the JNK pathway and AP-1. J. Biol. Chem. 278, 36993-36998. https://doi.org/10.1074/jbc.M302942200
- Otterbein, L. E., Bach, F. H., Alam, J., Soares, M., Tao Lu, H., Wysk, M., Davis, R. J., Flavell, R. A. and Choi, A. M. 2000. Carbon monoxide has anti-inflammatory effects involving the mitogen-activated protein kinase pathway. Nat. Med. 6, 422-428. https://doi.org/10.1038/74680
- Paine, A., Eiz-Vesper, B., Blasczyk, R. and Immenschuh, S. 2010. Signaling to heme oxygenase-1 and its anti-inflammatory therapeutic potential. Biochem. Pharmacol. 80, 1895-1903. https://doi.org/10.1016/j.bcp.2010.07.014
- Ravindranathan, P., Pasham, D., Balaji, U., Cardenas, J., Gu, J., Toden, S. and Goel, A. 2018. Mechanistic insights into anticancer properties of oligomeric proanthocyanidins from grape seeds in colorectal cancer. Carcinogenesis 39, 767-777. https://doi.org/10.1093/carcin/bgy034
- Rochette, L., Cottin, Y., Zeller, M. and Vergely, C. 2013. Carbon monoxide: mechanisms of action and potential clinical implications. Pharmacol. Ther. 137, 133-152. https://doi.org/10.1016/j.pharmthera.2012.09.007
- Sarady-Andrews, J. K., Liu, F., Gallo, D., Nakao, A., Overhaus, M., Ollinger, R., Choi, A. M. and Otterbein, L. E. 2005. Biliverdin administration protects against endotoxin-induced acute lung injury in rats. Am. J. Physiol. Lung Cell Mol. Physiol. 289, L1131-L1137. https://doi.org/10.1152/ajplung.00458.2004
- Shahat, A. A., Ismail, S. I., Hammouda, F. M., Azzam, S. A., Lemiere, G., De Bruyne, T., De Swaef, S., Pieters, L. and Vlietinck, A. 1998. Anti-HIV activity of flavonoids and proanthocyanidins from Crataegus sinaica. Phytomedicine 5, 133-136. https://doi.org/10.1016/S0944-7113(98)80010-X
- Shapouri-Moghaddam, A., Mohammadian, S., Vazini, H., Taghadosi, M., Esmaeili, S. A., Mardani, F., Seifi. B., Mohammadi, A., Afshari, J. T. and Sahebkar, A. 2018. Macrophage plasticity, polarization, and function in health and disease. J. Cell. Physiol. 233, 6425-6440.
- Srisook, K., Han, S. S., Choi, H. S., Li, M. H., Ueda, H., Kim, C. and Cha, Y. N. 2006. CO from enhanced HO activity or from CORM-2 inhibits both O2- and NO production and downregulates HO-1 expression in LPS-stimulated macrophages. Biochem. Pharmacol. 71, 307-318. https://doi.org/10.1016/j.bcp.2005.10.042
- Su, X., Howell, A. B. and D'Souza, D. H. 2010. Antiviral effects of cranberry juice and cranberry proanthocyanidins on foodborne viral surrogates--a time dependence study in vitro. Food Microbiol. 27, 985-991. https://doi.org/10.1016/j.fm.2010.05.027
- Takeda, T. A., Sasai, M., Adachi, Y., Ohnishi, K., Fujisawa, J. I., Izawa, S. and Taketani, S. 2017. Potential role of heme metabolism in the inducible expression of heme oxygenase-1. Biochim. Biophys. Acta Gen. Subj. 1861, 1813-1824. https://doi.org/10.1016/j.bbagen.2017.03.018
- Yang, G., Li, Y., Wu, W., Liu, B., Ni, L., Wang, Z., Miao, S., Wang, L. and Liu, C. 2015. Anti-oxidant effect of heme oxygenase-1 on cigarette smoke-induced vascular injury. Mol. Med. Rep. 12, 2481-2486. https://doi.org/10.3892/mmr.2015.3722
- Yang, L., Xian, D., Xiong, X., Lai, R., Song, J. and Zhong, J. 2018. Proanthocyanidins against oxidative stress: From molecular mechanisms to clinical applications. Biomed. Res. Int. 2018, 8584136.
- Wang, Y. R., Chen, K. L., Li, C. M., Li, L. and Wang, G. L. 2019. Heme oxygenase 1 regulates apoptosis induced by heat stress in bovine ovarian granulosa cells via the ERK1/2 pathway. J. Cell. Physiol. 234, 3961-3972. https://doi.org/10.1002/jcp.27169
- Zhang, R. G., Pan, K., Hao, Y., Yip, C. Y. and Ko, W. H. 2019. Anti-inflammatory action of HO-1/CO in human bronchial epithelium in response to cationic polypeptide challenge. Mol. Immunol. 105, 205-212. https://doi.org/10.1016/j.molimm.2018.12.002