1.Effects of Yizhikoufuye on apoptosis in different cerebral regions of rats with Alzheimer's disease
Yan ZHAN ; Dihui MA ; Yu ZHANG
Journal of Jilin University(Medicine Edition) 2006;0(01):-
Objective To observe the effect of YiZhikoufuye(YZ) on apoptosis in the different cerebral regions of experimental Alzheimer's disease(AD) rats.Methods The animal model of AD was set up by stereotaxic damage of CA1 area of rat hippocampus using aggressive A?1-40.After operation thirty male Wistar rats were randomly divided into YZ,melatonin and model control groups,10 in each group.The rats were fed with YZ, melatonin and saline,respectively.On the 41th day,the rats were killed.The percentage of apoptotic cells,the changes of mitochondrial membrane potential and the expression level of cytochrome C protein were observed with immunohistochemical methods.Results Compared with control group,YZ could inhibit the apoptotic changes caused by A?(P
2.Application of the Humanistic Care in Emergency Orthopedics
Dihui ZHANG ; Manli LONG ; Fang LI
Chinese Medical Ethics 2018;31(7):901-904
Patients with orthopedicsin emergency department generally show psychological characteristics such as panic,sadness,conflictand worry.However,under the current circumstances,humanistic care is difficult to im-plement in orthopedics work due to the shortness of time for admission,the lack of medical human resources and the indifference of humanistic care concept in hospitals.On this basis,this paper put forward the suggestions for im-plementing humanistic care: timely dealing with injuries,choosing appropriate communication methods,implemen-ting lean medical care and meeting the reasonable needs of patients.
3.The role of LncRNA00602 in Ad36-induced differentiation of adipocytes
Jiale GAO ; Xiaozheng ZHANG ; Yi JIAO ; Nurmaimaiti NURBIYE ; Xuanyu MENG ; Youzongsheng XU ; Bingli WANG ; Dihui LIU ; Yaqun GUAN
Chinese Journal of Endocrinology and Metabolism 2021;37(6):558-566
Objective:To investigate the possible role of long non-coding RNA (LncRNA) 00602 in promoting browning in adipocytes induced by adenovirus type 36 (Ad36).Methods:According to Ad36 infection, adipose tissue samples of obese patients were divided into Ad36-negative group and Ad36-infected group. Realtime fluorescent quantitative PCR (qRT-PCR) was used to detect the changes in the expression of LncRNA00602 mRNA in omental adipose tissue of the two groups, and analyze the differences between the two groups. The correlation between waist-to-hip ratio, systolic blood pressure, diastolic blood pressure, fasting blood glucose, triacylglyceride and other indicators of the patients in the group with LncRNA00602 mRNA expression were analyzed. HE staining was used to detect the size of adipocytes in the omental adipose tissue of the Ad36 negative group and the Ad36 infection group. qRT-PCR and Western blotting were used to detect the mRNA and protein expression levels of uncoupling protein 1 (UCP1) and PR domain containing 16 (PRDM16) in omental adipose tissue of two groups of patients. Human adipose-derived stem cells (hADSC) were isolated and cultured, using Ad36 to induce differentiation, and divided into control group and LncRNA00602 knockdown group. On 0, 2, and 4 days after LncRNA00602 knockdown, fluoroboron dipyrrole (BODIPY) and mitochondrial red fluorescence (Mito-Tracker Red) were used to stain intracellular lipid droplets and mitochondria. At the same time, qRT-PCR and Western blotting were used to detect changes in the expression of UCP1 and PRDM16.Results:The expression of LncRNA00602 gene in the Ad36 infection group was higher than that in the Ad36 negative group (all P<0.05). The expression of LncRNA00602 in the Ad36 negative group was not significantly different from the above clinical indicators, while the expression of LncRNA00602 was negatively correlated with serum fasting blood glucose and triacylglyceride ( r=-0.522, -0.486, P<0.05) in the Ad36 infection group; HE staining showed that the average adipocyte area of the Ad36 infection group was smaller than that of the Ad36 negative group. At the same time, UCP1 and PRDM16 gene expression were higher than the negative group (all P<0.05). At the cellular level, on the 2nd and 4th days after knockdown of LncRNA00602, the lipid droplet area of adipocytes in the LncRNA00602 knockdown group was larger than that of the control group, the number of mitochondria decreased compared with the control group, and difference was statistically significant ( P<0.05 or P<0.01); Compared with the control group, there was significantly lower expression of the browning marker genes UCP1, PRDM16, and protein in the adipocytes in the LncRNA00602 knockdown group (all P<0.05). Conclusion:In Ad36-induced adipocyte differentiation, LncRNA00602 may positively regulate the expression of UCP1, PRDM16 and lipid droplet metabolism, and promote the browning of adipocytes.