Effect of Prescription of Turbidity-Resolving and Lipid-Eliminating on Visfatin Level,Oxidative Stress and Hepatocyte Apoptosis in Rats with Type 2 Diabetes Complicated with Hyperlipidemia
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Effect of Prescription of Turbidity-Resolving and Lipid-Eliminating on Visfatin Level,Oxidative Stress and Hepatocyte Apoptosis in Rats with Type 2 Diabetes Complicated with Hyperlipidemia
FANG Dan, TIAN Liping, ZHOU Zhihuan. Effect of Prescription of Turbidity-Resolving and Lipid-Eliminating on Visfatin Level,Oxidative Stress and Hepatocyte Apoptosis in Rats with Type 2 Diabetes Complicated with Hyperlipidemia. [J]. 20(6):670-674(2020)
FANG Dan, TIAN Liping, ZHOU Zhihuan. Effect of Prescription of Turbidity-Resolving and Lipid-Eliminating on Visfatin Level,Oxidative Stress and Hepatocyte Apoptosis in Rats with Type 2 Diabetes Complicated with Hyperlipidemia. [J]. 20(6):670-674(2020) DOI: 10.14009/j.issn.1672-2124.2020.06.009.
Effect of Prescription of Turbidity-Resolving and Lipid-Eliminating on Visfatin Level,Oxidative Stress and Hepatocyte Apoptosis in Rats with Type 2 Diabetes Complicated with Hyperlipidemia
OBJECTIVE: To probe into the effect of prescription of turbidity-resolving and lipid-eliminating on visfatin level
oxidative stress and hepatocyte apoptosis in rats with type 2 diabetes complicated with hyperlipidemia.METHODS: 60 healthy SD rats were selected
after 1-week feeding
6 rats were brought into normal group and 54 rats were brought into model group according to random weight grouping method. The normal group was fed with conventional fodder
while the model group was fed with high-sugar and high-fat fodder. After 8 weeks
rats in the model group were intraperitoneally injected with 2% streptozotocin to prepare rat model of type 2 diabetes complicated with hyperlipidemia
36 rats with significant differences from the normal group were selected for study and divided into model group
metformin group
Zhibituo capsule group and turbidity-resolving and lipid-eliminating group( low
medium and high dose) via randomized block
with 6 rats in each group. Intragastric administration was given to rats in each group
after 1-month treatment
the visfatin level
oxidative stress [superoxide dismutase( SOD)
malonaldehyde( MDA)
advanced glycosylation end products( AGEs) and advanced oxidation protein products( AOPP) ]
hepatocyte apoptosis
B-cell lymphoma-2( Bcl-2) and Bcl-2 associated X protein( Bax) expression were compared among each group. RESULTS: The visfatin level in model group was significantly higher than other groups
which was statistically different with that of normal group
low
medium and high dose of turbidity-resolving and lipideliminating group( P < 0. 05); the SOD level of model group was significantly lower than other groups
while the AGEs
MDA and AOPP levels were significantly higher than other groups
which were statistically different with those of normal group
medium and high dose of turbidity-resolving and lipid-eliminating group( P<0. 05)
the AOPP level of model group was statistically different with that of low dose of turbidity-resolving and lipid-eliminating group( P <0. 05). The cell apoptosis of model group was significantly higher than other group
which was statistically different with that of normal group
metformin group
low and medium dose of turbidity-resolving and lipid-eliminating group( P<0. 05). Cell proportion of model group at stationary phase( G0/G1) was significantly higher than that of normal group
with statistically significant difference( P< 0. 05); which was slightly higher than each administration group
with no statistically significant difference( P > 0. 05). The proliferation index of model group was significantly lower than that of normal group
with statistically significant difference( P < 0. 05); which was slightly lower than each administration group
with no statistically significant difference( P>0. 05). The fluorescence index( FI) of Bax protein expression of model group was significantly higher than that of normal group
low
medium
high dose of turbidityresolving and lipid-eliminating group; the FI of Bcl-2 protein expression was significantly lower than that of normal group
metformin group
low and medium dose of turbidity-resolving and lipid-eliminating group; the expression level of Bax/Bcl-2 protein were significantly higher than that of normal group
metformin group
low
medium and high dose of turbidity-resolving and lipid-eliminating group
with statistically significant differences( P<0. 05). CONCLUSIONS:Prescription of turbidity-resolving and lipid-eliminating can effectively reduce the visfatin level in rats with type 2 diabetes complicated with hyperlipidemia
and improve oxidative stress; which can reduce hepatocyte apoptosis by enhancing the expression of Bcl-2 protein and weakening the expression of Bax protein.
关键词
化浊清脂方2型糖尿病合并高脂血症内脂素氧化应激肝细胞凋亡
Keywords
Prescription of turbidity-resolving and lipid-eliminatingType 2 diabetes complicated with hyperlipidemiaVisfatinOxidative stressHepatocyte apoptosis
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