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Objective:To observe the effect of isorhmnetin on the ER/TGF-β1/Smad3 signaling pathways in human dermal fibroblasts (HSF) damaged by UVA.Methods:HSF were divided into control group, model group, estradiol group, isorhmnetin groups with 100, 10, 1, 0.1, 0.01, 0.001 μmol/L by random number table method, and cell photoaging models were established in all groups excepting the control group. After the intervention with corresponding drugs, cell proliferation rates were detected with MTT method, and the effective concentration of isorhmnetin was screened. Then the cells were divided into control group, model group, estradiol group, isorhmnetin group, TGF-β1 blocker group, Samd3 blocker group, and COL1A1 blocker group. Cell photoaging models were established in all groups excepting the control group. After intervened with corresponding drugs, the TGF-β1, Smad3, Ⅰ collagen α1 (collagen, type Ⅰ, alpha 1, COL1A1) mRNA and protein expression in all groups were detected by the real-time quantitative PCR and the Wester blot method.Results:The proliferation rate of isor administration group were increased than those in the control group ( P<0.01). Compared to the UVA irradiation group, the expression of TGF-β1 mRNA (0.956 ± 0.020 vs. 0.718 ± 0.036), Smad3 mRNA (0.981 ± 0.044 vs. 0.753 ± 0.047), COL1A1 mRNA (0.998 ± 0.032 vs. 0.786 ± 0.031), TGF-β1 protion (0.761 ± 0.026 vs. 0.542 ± 0.023), Smad3 protion (0.776 ± 0.016 vs. 0.551 ± 0.025), COL1A1 protion (0.792 ± 0.025 vs. 0.584 ± 0.012) in isor administration group significantly increased ( P<0.01). Compared to the isor administration group, the TGF-β1 mRNA (0.762 ± 0.051, 0.802 ± 0.012, 0.828 ± 0.030 vs. 0.967 ± 0.026), Smad3 mRNA (0.784 ± 0.027, 0.816 ± 0.015, 0.830 ± 0.032 vs. 0.998 ± 0.021), COL1A1 mRNA (1.082 ± 0.025, 1.101 ± 0.012, 1.138 ± 0.011 vs. 1.263 ± 0.022), TGF-β1 protion (0.675 ± 0.028, 0.682 ± 0.026, 0.722 ± 0.015 vs. 0.862 ± 0.014), Smad3 protion (0.712 ± 0.013, 0.764 ± 0.012, 0.778 ± 0.011 vs. 0.901 ± 0.015), COL1A1 protion (0.738 ± 0.016, 0.770 ± 0.038, 0.792 ± 0.026 vs. 0.964 ± 0.017) in the TGF-β1 blocker group, Smad3 blocker group and COL1A1 blocker group significantly decreased ( P<0.01). Conclusions:Isorhmnetin can promote the collagen synthesis of photo aging HSF cells, and its mechanism is related to the regulation of ERβ/TGF-β1 signaling pathway.
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Objective To investigate the value of clinical pharmacists in clinical treatment through the practice of clinical pharmacists participating in clinical drug treatment and providing pharmaceutical care to patients .Methods Clinical pharmacists were involved in therapeutic scheme making , medication education and drug effect and adverse reaction tracking of one patient of liver cir -rhosis complicated with pleural effusion .Results The effects of drug treatment were improved and the adverse drug reactions were re -duced after the participation of pharmacist in clinical treatment and the implementation of pharmaceutical care for the patient .Conclu-sion The participation of pharmacist in clinical drug therapy could enhance normative and reasonable usage of drugs .This participa-tion is decisive and valuable in clinical treatment .
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AIM:To investigate the anti-inflammatory effect of Musk Eye Drops(Moschus,Borneolum Syntheticum,etc.) METHODS:Anti-inflammatory effects of Musk Eye Drops on acute ceratitis in mice was observed with the models of mouse auricle edema induced by dimethylbenzene and acute conjunctivitis caused by Croton oil,and acute ceratitis resulting from surgical injury. RESULTS:All groups of Musk Eye Drops could significantly inhibit the edema,decrease the inflammatory of acute conjunctivitis and acute ceratitis.The effect of Musk Eye Drops had statistical significance(P0.05). CONCLUSION:Musk Eye Drops has obvious anti-inflammatory effect.