Mohammadi, E., Vatanpour, H., Hosseini Shirazi, F. (2015). Immunomodulatory Effects of Bee Venom in Human Synovial Fibroblast Cell Line. Iranian Journal of Pharmaceutical Research, 14(1), 313-320. doi: 10.22037/ijpr.2015.1613
Ebrahim Mohammadi; Hossein Vatanpour; Farshad Hosseini Shirazi. "Immunomodulatory Effects of Bee Venom in Human Synovial Fibroblast Cell Line". Iranian Journal of Pharmaceutical Research, 14, 1, 2015, 313-320. doi: 10.22037/ijpr.2015.1613
Mohammadi, E., Vatanpour, H., Hosseini Shirazi, F. (2015). 'Immunomodulatory Effects of Bee Venom in Human Synovial Fibroblast Cell Line', Iranian Journal of Pharmaceutical Research, 14(1), pp. 313-320. doi: 10.22037/ijpr.2015.1613
Mohammadi, E., Vatanpour, H., Hosseini Shirazi, F. Immunomodulatory Effects of Bee Venom in Human Synovial Fibroblast Cell Line. Iranian Journal of Pharmaceutical Research, 2015; 14(1): 313-320. doi: 10.22037/ijpr.2015.1613
Immunomodulatory Effects of Bee Venom in Human Synovial Fibroblast Cell Line
1Department of Toxicology and Pharmacology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Kurdistan University of Medical Sciences, Sanandaj, Iran.
2Department of Toxicology and Pharmacology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
3Pharmaceutical Sciences Research Center, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract
As in Iranian traditional medicine, bee venom (BV) is a promising treatment for the rheumatoid arthritis (RA) which is considered as a problematic human chronic inflammatory disease in the present time. Smoking is considered to be a major risk factor in RA onset and severity. The main aim of this study is to investigate the effects of BV on cigarette smoke-induced inflammatory response in fibroblast-like synoviocytes (FLS). Cytotoxicity of cigarette smoke condensate (CSC) and bee venom were determined by the tetrazolium (MTT) method in cultured synovial fibroblastes. The expression of interleukin-1β and sirtuin1 mRNA were analyzed by SYBR green real-time quantitative PCR. Differences between the mean values of treated and untreated groups were assessed by student t-test. Based on MTT assay, CSC and BV did not exert any significant cytotoxic effects up to 40 µg/mL and 10 µg/mL, respectively. Our results showed that interleukin-1β mRNA level was significantly up-regulated by CSC treatments in LPS-stimulated synoviocytes in a dose-dependent manner. Conversely, the expressions of IL-1β and Sirt1 were up-regulated even in lower concentrations of BV and attenuated at higher concentrations. Also, BV attenuated the CSC-induced and LPS-induced inflammatory responses in synovial fibroblasts. Our results support the epidemiological studies indicating pro-inflammatory effects of CSC and anti-inflammatory effects of BV on FLS cell line.
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