[Objective] The study aimed to explore the protective effects of LBP-Ⅳ on blood vessel endothelium function induced by paraoxon(PARA) and the potential mechanisms. [Method] The ex vivo aorta pectoralis vascular ri...[Objective] The study aimed to explore the protective effects of LBP-Ⅳ on blood vessel endothelium function induced by paraoxon(PARA) and the potential mechanisms. [Method] The ex vivo aorta pectoralis vascular ring (EVAPVR) of rats and cultured human umbilical vein endothelial cells (HUVEC) were exposed to medium contained paraoxon (3.63 μmol/L), LBP-Ⅳ for different concentration were used to inhibit the damage effect. The endothelial-dependent relaxation reaction (EDRR), endothelial cell monolayer permeability(ECMP), biochemical index were measured.[Result] LBP-Ⅳ dose dependently (0.1, 1, 10 mg/ml) reduced the inhibition of ACh-induced EDRR and the increased ECMP induced by PARA, simultaneously LBP-Ⅳ(10 mg/ml) also protected the SOD activity, inhibited the increase of the MDA content and reduction of NO content induced by PARA in medium of cultured HUVEC. [Conclusion] LBP-Ⅳ could protect the blood vessel endothelium function from being impaired by PARA, and the potential mechanism was possibly concerned with the antioxidation of LBP-Ⅳ.展开更多
The results of injecting of autologic mesenchymal stem cells of bone marrow origin (AMSCBMO), transfected by the GFP gene, into the scar of rat uterine horns were studied by methods of light microscopy. After the intr...The results of injecting of autologic mesenchymal stem cells of bone marrow origin (AMSCBMO), transfected by the GFP gene, into the scar of rat uterine horns were studied by methods of light microscopy. After the introduction of AMSCBMO into the formed scar on the right (2 months after the ligation) large groups of blood vessels with cellular elements inside were present;groups like that were not found in the opposite side. Studying unstained sections under reflected ultraviolet light the sufficient bright luminescence in the endothelium and the external membrane of scar vessels was found in uterine horn only on the side of introduction of AMSCBMO. It was concluded that after the introduction of AMSCBMO into the scar tissue they form blood vessels by differentiation into endotheliocytes and pericytes. GFP gene expression not only in endothelium of vessels, but also in their external membrane indicates that differentiation of AMSCMBO is possible in endothelial and in pericytal directions.展开更多
Objective To observe therapeutic effects of acupuncture on the mouse of hyperlipemia and to explore the mechanisms. Methods One hundred and twenty Kunming mice, male, sanitary degree, were randomly divided into normal...Objective To observe therapeutic effects of acupuncture on the mouse of hyperlipemia and to explore the mechanisms. Methods One hundred and twenty Kunming mice, male, sanitary degree, were randomly divided into normal group (n=40), a model group (n=40), an acupuncture group (n=20) and a medicine group (n=20). Except the normal group, the mice were fed with high fat forage to prepare mouse hyperlipemia model. On the 15th day of modeling, serum total cholesterol (TC), triglyceride (TG), low density lipoprotein-cholesterol (LDL-C), high density lipoprotein-cholesterol (HDL-C) levels were detected in 20 normal mice and 20 model mice; electroacupuncture was given at bilateral "Fēnglóng" (丰隆 ST 40), "Qūchí" (曲池 LI 11), "Sānyīnjiāo" (三阴交 SP 6) in the acupuncture group, once a day, for 10 consecutive days; in the medicine group, the mice were intragastrically administrated with Simvastatin, once daily , for 10 consecutive days. After the end of treatment, serum TC, TG, LDL-C, HDL-C, malondialdehyde (MDA), nitric oxide (NO) and endothelin (ET) contents and superoxide dismutase (SOD) activities were detected in the groups. Results On the 15th day of modeling, in the model group serum TG, TC, LDL-C contents were significantly higher (all P〈0.05) and HDL-C content was significantly lower (P〈0.01) than those in the normal group. After treatment for 10 days, in the acupuncture group and the medicine group serum TG, TC, LDL-C, MDA and ET contents were significantly lower and serum HDL-C and NO contents and SOD activities were significantly higher than those in the model group (P〈0.05, P〈0.01), and the improving action in the acupuncture group was better than that in the medicine group (P〈0.05, P〈0.01). Conclusion Acupuncture can regulate fat metabolism, resist lipid peroxidation and protect vascular endothelial function in the mouse of hyperlipemia.展开更多
Objective: To evaluate the protective effect of propyl gallate (PG), an alkyl ester of gallic acid which is an active ingredient of Radix Paeoniae, against oxidized low-density lipoprotein (ox-LDL)-induced apopto...Objective: To evaluate the protective effect of propyl gallate (PG), an alkyl ester of gallic acid which is an active ingredient of Radix Paeoniae, against oxidized low-density lipoprotein (ox-LDL)-induced apoptosis and death in endothelial cells (ECs) and to find out its preliminary mechanism. Methods: The cultured endothelial cells were divided into normal, model (ox-LDL), control (fetal bovine serum), PG high dose (20 p,g/mL), PG middle dose (10 μg/mL), and PG low dose (5 μg/mL) groups, each derived from three different pools of umbilical cords. The model of injured human umbilical vein endothelial cells (HUVECs) was induced by ox-LDL. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay, Hoechst 33258 staining, flow cytometry and measurement of nitrogen monoxidum (NO) release were used to evaluate the protective effect of PG against ox-LDL-induced apoptosis and death in HUVECs. To find out the mechanism of this protective effect, the expression of endothelial nitric oxide synthase (eNOS) mRNA, eNOS protein expression, immunofluorescence of intracellular reactive oxygen species (ROS) and activities of malondialdehyde (MDA), superoxidedismutase (SOD) and glutathione peroxidase (GPx) were observed. Results: PG significantly reduced ox-LDL-induced apoptosis and cell death. The percentage of cells death and apoptosis was significantly higher in the ox-LDL group than that in the control group (P〈0.05). Compared with the control group, the cells death and apoptosis of PG group was no different (P〉0.05). As compared with the ox-LDL group, results of the PG high dose group showed that cell viability was significantly increased (P〈0.05), the level of NO release, expression of eNOS mRNA, densitometric value of eNOS protein expression, as well as the activities of SOD and GPx were all significantly higher (all P〈0.05). Conclusion: PG could potentially serve as a novel endothelial protective agent against ox-LDL-induced injury of endothelial cell.展开更多
基金Supported by Natural Science Research Projects2010,Education Department of Henan Province(2010B330002)~~
文摘[Objective] The study aimed to explore the protective effects of LBP-Ⅳ on blood vessel endothelium function induced by paraoxon(PARA) and the potential mechanisms. [Method] The ex vivo aorta pectoralis vascular ring (EVAPVR) of rats and cultured human umbilical vein endothelial cells (HUVEC) were exposed to medium contained paraoxon (3.63 μmol/L), LBP-Ⅳ for different concentration were used to inhibit the damage effect. The endothelial-dependent relaxation reaction (EDRR), endothelial cell monolayer permeability(ECMP), biochemical index were measured.[Result] LBP-Ⅳ dose dependently (0.1, 1, 10 mg/ml) reduced the inhibition of ACh-induced EDRR and the increased ECMP induced by PARA, simultaneously LBP-Ⅳ(10 mg/ml) also protected the SOD activity, inhibited the increase of the MDA content and reduction of NO content induced by PARA in medium of cultured HUVEC. [Conclusion] LBP-Ⅳ could protect the blood vessel endothelium function from being impaired by PARA, and the potential mechanism was possibly concerned with the antioxidation of LBP-Ⅳ.
文摘The results of injecting of autologic mesenchymal stem cells of bone marrow origin (AMSCBMO), transfected by the GFP gene, into the scar of rat uterine horns were studied by methods of light microscopy. After the introduction of AMSCBMO into the formed scar on the right (2 months after the ligation) large groups of blood vessels with cellular elements inside were present;groups like that were not found in the opposite side. Studying unstained sections under reflected ultraviolet light the sufficient bright luminescence in the endothelium and the external membrane of scar vessels was found in uterine horn only on the side of introduction of AMSCBMO. It was concluded that after the introduction of AMSCBMO into the scar tissue they form blood vessels by differentiation into endotheliocytes and pericytes. GFP gene expression not only in endothelium of vessels, but also in their external membrane indicates that differentiation of AMSCMBO is possible in endothelial and in pericytal directions.
基金Supported by The Hebei Province TCM Administra on Bureau Founda on for Tackling Key Problems of Science and Technology: 2009058
文摘Objective To observe therapeutic effects of acupuncture on the mouse of hyperlipemia and to explore the mechanisms. Methods One hundred and twenty Kunming mice, male, sanitary degree, were randomly divided into normal group (n=40), a model group (n=40), an acupuncture group (n=20) and a medicine group (n=20). Except the normal group, the mice were fed with high fat forage to prepare mouse hyperlipemia model. On the 15th day of modeling, serum total cholesterol (TC), triglyceride (TG), low density lipoprotein-cholesterol (LDL-C), high density lipoprotein-cholesterol (HDL-C) levels were detected in 20 normal mice and 20 model mice; electroacupuncture was given at bilateral "Fēnglóng" (丰隆 ST 40), "Qūchí" (曲池 LI 11), "Sānyīnjiāo" (三阴交 SP 6) in the acupuncture group, once a day, for 10 consecutive days; in the medicine group, the mice were intragastrically administrated with Simvastatin, once daily , for 10 consecutive days. After the end of treatment, serum TC, TG, LDL-C, HDL-C, malondialdehyde (MDA), nitric oxide (NO) and endothelin (ET) contents and superoxide dismutase (SOD) activities were detected in the groups. Results On the 15th day of modeling, in the model group serum TG, TC, LDL-C contents were significantly higher (all P〈0.05) and HDL-C content was significantly lower (P〈0.01) than those in the normal group. After treatment for 10 days, in the acupuncture group and the medicine group serum TG, TC, LDL-C, MDA and ET contents were significantly lower and serum HDL-C and NO contents and SOD activities were significantly higher than those in the model group (P〈0.05, P〈0.01), and the improving action in the acupuncture group was better than that in the medicine group (P〈0.05, P〈0.01). Conclusion Acupuncture can regulate fat metabolism, resist lipid peroxidation and protect vascular endothelial function in the mouse of hyperlipemia.
文摘Objective: To evaluate the protective effect of propyl gallate (PG), an alkyl ester of gallic acid which is an active ingredient of Radix Paeoniae, against oxidized low-density lipoprotein (ox-LDL)-induced apoptosis and death in endothelial cells (ECs) and to find out its preliminary mechanism. Methods: The cultured endothelial cells were divided into normal, model (ox-LDL), control (fetal bovine serum), PG high dose (20 p,g/mL), PG middle dose (10 μg/mL), and PG low dose (5 μg/mL) groups, each derived from three different pools of umbilical cords. The model of injured human umbilical vein endothelial cells (HUVECs) was induced by ox-LDL. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay, Hoechst 33258 staining, flow cytometry and measurement of nitrogen monoxidum (NO) release were used to evaluate the protective effect of PG against ox-LDL-induced apoptosis and death in HUVECs. To find out the mechanism of this protective effect, the expression of endothelial nitric oxide synthase (eNOS) mRNA, eNOS protein expression, immunofluorescence of intracellular reactive oxygen species (ROS) and activities of malondialdehyde (MDA), superoxidedismutase (SOD) and glutathione peroxidase (GPx) were observed. Results: PG significantly reduced ox-LDL-induced apoptosis and cell death. The percentage of cells death and apoptosis was significantly higher in the ox-LDL group than that in the control group (P〈0.05). Compared with the control group, the cells death and apoptosis of PG group was no different (P〉0.05). As compared with the ox-LDL group, results of the PG high dose group showed that cell viability was significantly increased (P〈0.05), the level of NO release, expression of eNOS mRNA, densitometric value of eNOS protein expression, as well as the activities of SOD and GPx were all significantly higher (all P〈0.05). Conclusion: PG could potentially serve as a novel endothelial protective agent against ox-LDL-induced injury of endothelial cell.