大黄素对脑出血大鼠血肿周围脑组织含水量、肿瘤坏死因子-α和谷氨酸表达水平的影响

目的:探讨大黄素对脑出血大鼠血肿周围脑组织含水量、肿瘤坏死因子-α和谷氨酸表达水平的影响及其治疗脑水肿的可能机制。方法:取自体股动脉血约100μL,注入大鼠纹状体区域,采用随机分组法分为大黄素治疗组、假手术组和模型对照组3组,每组30只。假手术组和模型对照组以生理盐水灌胃,每次给药剂量为6μL/g体质量,1 d 2次;大黄素治疗组在造模成功后以6 g/L大黄素混悬液灌胃,给药剂量为100μg/g体质量,1 d 1次。术后通过大鼠改良Bederson评分进行行为学评定,干湿重法测脑组织含水量,双抗体夹心ELISA法检测脑组织肿瘤坏死因子-α(TNF-α)含量,免疫组化法检测脑组织中谷氨酸(glutamate,Glu)表达。结果:模型对照组的改良Bederson评分明显高于同时间点的假手术组(P<0.05);各时间点的大黄素治疗组的改良Bederson评分均低于同时间点的模型对照组(P<0.05)。模型对照组血肿周围脑组织含水量、TNF-α和Glu与同时间点的假手术组对比,差别均有统计学意义(P<0.05);造模后第5天脑组织含水量、TNF-α和Glu表达均达最高值,3个指标之间呈正相关性。大黄素治疗组血肿周围脑组织含水量、TNF-α和Glu较同时间点的模型对照组均降低,差别均有统计学意义(P<0.05),且3个指标在第5天均达最高值,3者之间呈正相关性。结论:脑出血大鼠出现明显的脑水肿和神经功能损伤,且出血后TNF-α和Glu在第5天达到最高值,可能的生物学效应机制是大黄素抑制炎性因子的释放、降低谷氨酸的表达水平。

Inhibitory effect of emodin and Astragalus polysaccharide on the replication of HBV

AIM: To evaluate the anti-viral effect of emodin plus Astragalus polysaccharide (APS) in hepatitis B virus (HBV) transgenic mice.METHODS: Sixty HBV transgenic mice (HBV TGM) whose weight varied between 18 and 24 g were randomly divided into 3 groups, with 20 mice in each group. Group A was the normal control, where the mice were treated with physiological saline; group B was the positive control where the mice were treated with lamivudine solution (100 mL/kg per day). Group C was the experimental group where the mice were treated with physiological saline containing emodin and APS (57.59 mg/kg per day and 287.95 mg/kg per day, respectively). The mice were treated daily for 3 wk. After 1 wk recovery time, the mice were sacrifi ced and serum as well as liver tissues were collected for ELISA and histological examination.RESULTS: After 21 d treatment, HBV DNA levels in group B and group C significantly declined when compared with group A (P < 0.05). However, a signif icant increase in HBV DNA content was observed in group B, whereas this phenomenon was not observed in group C. A reduction in the contents of HBsAg, HBeAg and HBcAg in the mice from group B and C was observed when compared with group A.CONCLUSION: Emodin and APS have a weak but persistent inhibitory effect on HBV replication in vivo, which may function as a supplementary modality in the treatment of hepatitis B infection.

Inhibitory effect of schisandrin B on gastric cancer cells in vitro

AIM： To investigate the inhibitory effect and possible mechanism of action of schisandrin B in SC-B on gastric cancer cells in vitro.METHODS： SC-B consisted of schisandrin B, aloeemodin, and Astragalus polysaccharides. Exponentially growing human gastric cancer SGO7901 cells were divided into six treatment groups： （1） control group （RPMI 1640 medium）; （2） negative control group （2% DMSO）; （3） positive control group （50 mg/L 5-Fluorouracil, 5-FU）; （4） low-dose group （LSC, final concentration of schisandrin B, 25 mg/L）, （5） moderate-dose group （MSC, final concentration of schisandrin B, 50 mg/L）; （6） highdose group （HSC, final concentration of schisandrin B, 100 mg/L）. Follow-up was done at 12-48 h. An MTT （Methylthiazolyldiphenyl-tetrazolium bromide） assay was used to examine the inhibitory effect of SOB on gastric cancer cells. The mitosis index was assessed using an inverted microscope. Flow cytometry was used to visualize the cell cycle. An RT-PCR （Reverse transcription-Polymerase chain reaction） -based assay was used to detect mRNA expression for cyclin D1 and glyceraldehyde-3-phosphate dehydrogenase （GAPDH）.RESULTS： The MTT assay showed that the number of living cells in the LSC, MSC and HSC groups was significantly smaller than that in the DMSO-treated group （P 〈 0.05） at 12-48 h. The inhibitory rate （IR） of the LSC group was 41.15% ± 3.86%, 59.24% ± 5.34% and 69.93% ± 7.81% at 12, 24 and 48 h, respectively. The IR of the MSC group was 42.82% ± 4.94%, 62.68% ± 7.58% and 71.79% ± 8.12% at 12, 24 and 48 h, respectively. The IR of the HSC group was 37.50% ± 3.21%, 40.34% ± 2.98% and 61.99% ± 4.88% at 12, 24 and 48 h, respectively. These results suggested that a moderate dosage had the most obvious inhibitory efficacy at 48 h. Compared to the DMSO group, the mitosis index of the LSC, MSC, HSC groups was greatly decreased （P 〈 0.05） at all time points. Any dose of SC-B suppressed mitosis within 12-48 h. Compared to the DMSO group, the percentage of cells in the G0/G1 phase of the MSC group was greatly increased, and that of the S ＋ G2M phase was greatly decreased, while the percentage of cell inhibition （PCI） in the MSC group was greatly increased （P 〈 0.05）. This suggested that SC-B could exclusively arrest cells in the G0/G1 phase. Cyclin D1 mRNA expression was lower in the MSC group than that in the DMSO group （P 〈 0.05）.CONCLUSION： SC-B can inhibit the proliferation and aberrant mitosis of human gastric cancer SCG-7901 cells /n v/tro, This inhibitory effect may be due to the down- regulation of cyclin D1 mRNA expression, which causes cell cycle arrest of gastric cancer cells.

Protective Effect of Emodin against Lipopolysaccharides-induced Corneal Injury in Rats

Objective To investigate the effect of emodin on lipopolysaccharides （LPS）-induced corneal injury in rats. Methods Three parallel incisions on the central surface of corneal epithelium were made and LPS was applied on them to induce corneal injury in Wistar rats. All rats were randomly divided into emodin group （n=40） and keratitis group （n=40）. Rats in the emodin group received subconjunctival injection of emodin and rats in the keratitis group received its vehicle 30 minutes before LPS exposure. At different time points-1 3, 6, 12, and 24 hours after LPS exposure, the symptoms of all rats were observed and the severity of their ocular inflammation was examined with a slit lamp microscope, then 8 rats in each group were killed through cervical dislocation and their eyes were enucleated and prepared to observe pathological changes of corneal tissue under a light microscope. The activation of nuclear factor-loB （NF-κB） under different condi- tions was determined by Western blot. Immunocytochemistry staining with an antibody against intercellular adhesion molecule-1 （ICAM-1） was performed to identify positive cells in corneal tissues. Results The model of acute keratitis was successfully established in Wistar rats. LPS could induce a typical corneal inflammatory response, such as hyperemia, corneal edema and opacity, which were observed in model rats. Compared with keratitis group, both ocular behaviors and damages of the corneal structure were improved in emodin group. Furthermore, the activation of NF-κB and the expression of ICAM-1 induced by LPS were markedly inhibited in emodin group. Conclusion Emodin can inhibit the activation of NF-κB and the expression of ICAM-I induced by LPS in corneas, protect against acute corneal injury, and improve symptoms in rats.