1.Effects of N-carbamylglutamic on growth performance,blood biochemistry,antiox-idant indicators and meat quality of meat rabbits
Xin YE ; Yingchun SHEN ; Mengdi XUE ; Xiuju WU ; Jing LI ; Jingzhi LYU
Chinese Journal of Veterinary Science 2024;44(9):2055-2062
To reveal the effects of N-carbamylglutamic(NCG)on growth performance,blood pa-rameters and meat quality of meat rabbits,192 Hyla rabbits at 35 days of age were assigned to four groups randomly with 0.00%,0.05%,0.10%,and 0.20%NCG added to the basal diet,with six replicates of eight rabbits in each group and one replicate of eight rabbits.The results indicated that:compared to the control group,the body weight of the 0.20%NCG group at d 35(P<0.01),the BW at d 14 and the average daily gain(ADG)from d 1 to 14 in the 0.05%NCG group(P<0.05)were significantly elevated;the ADG of the control group from d 1 to 35 was significantly lower than the 0.10%and 0.20%NCG groups(P<0.05).The levels of total superoxide dismutase(T-SOD)in the 0.10%NCG group(P<0.01),total antioxidant capacity(T-AOC)and urea nitro-gen(BUN)in the 0.20%NCG group(P<0.05)were significantly higher compared to the control group;the levels of T-SOD in the 0.10%NCG group were significantly elevated compared to the 0.05%NCG group(P<0.05).NCG significantly increased polyunsaturated fatty acids(PUFA)and PUFA/SFA(P<0.05).The cooked meat rate of the longissimus lumborum in the 0.20%NCG group was significantly increased compared to the control group(P<0.01),while the water holding rate of the longissimus lumborum increased significantly in the 0.10%NCG groups(P<0.01)and the control group(P<0.05)and 0.05%NCG group(P<0.05)than the 0.20%NCG group.NCG significantly reduced the crypts depth(P<0.01)and had the tendency to in-crease the V/C value(P=0.067),while the villi height of jejunal in the 0.20%NCG group was significantly elevated compared to the control group(P<0.05).In conclusion,NCG could promote the growth performance,enhance the antioxidant capacity,and improve the intestinal morphology and meat quality of meat rabbits.The appropriate amount of NCG added to meat rabbit diet is 0.10%.
2.Exploration of PBL and mini-CEX in the clinical probation teaching for medical students of eight-year program in hematology department
Jie XIAO ; Liping MA ; Danian NIE ; Shuangfeng XIE ; Yiqing LI ; Xiuju WANG ; Yudan WU ; Hongyun LIU
Chinese Journal of Medical Education Research 2018;17(8):822-825
Objective The study explored the feasibility of PBL teaching approach and mini-CEX scores evaluation method in hematology probation teaching practice. Methods 54 medical students of eight-year program were selected in the study and they were in hematology department of Sun Yat-sen Memorial Hospital for clinical probation. The study compared PBL teaching approach with traditional training method, and used mini-CEX to evaluate the students' clinical competence. Results The performance of PBL teaching group is better than traditional teaching group in the aspect of inquiry skill, clinical diagnosis, therapy plan and humanistic care (P<0.05). There is no significant difference of basic knowledge, physical examination skill and clinical operational skills between these two groups. More than 85%of the students in PBL group are satisfied with the teacher in the aspect of participation, feedback, guidance, correction and assistance. Conclusion Through this teaching practice, the study provides new methods for improving the teaching of pre-internal clinical practice in hematology department.
3.Role of ACE2-Ang (1-7)-Mas receptor axis in heart failure with preserved ejection fraction with hypertension.
Jiangbiao YU ; Yonggang WU ; Yinzhuang ZHANG ; Licheng ZHANG ; Qilin MA ; Xiuju LUO
Journal of Central South University(Medical Sciences) 2018;43(7):738-746
To investigate changes in the angiotensin converting enzyme 2 (ACE2) and angiotensin (1-7) [Ang (1-7)] and to explore the role of ACE2-Ang (1-7)-Mas receptor axis in hypertension with heart failure with preserved ejection fraction (HFPEF).
Methods: A total of 70 patients with primary hypertension and preserved left ventricular ejection fraction (LVEF>50%) were recruited and patients were divided into a hypertension group (HBP) and a heart failure with preserved ejection fraction group (HFpEF) according to the diagnostic criteria of HFpEF. Thirty-five healthy participants were selected randomly as a control group. Enzyme linked immunosorbent assays (ELISA) method was used to detect concentration of Ang (1-7), ACE2, angiotensin II (Ang II), brain natriuretic peptide (BNP) in plasma. Male Sprague- Dawley (SD) rats was randomly divided into 2 groups: An HFpEF group (n=16) and a sham group (n=8). Rats (n=8) in the AAC group were given Ang (1-7) [0.5 mg/(kg.d), intraperitoneally] for 6 weeks, and the rest were given equal dose normal saline. Then all the rats were killed, and the hearts were taken out for hematoxylineosin (HE) staining. The protein expressions of angiotensin converting enzyme (ACE), ACE2, and Mas receptor were detected by Western blot.
Results: The BNP and Ang II were significantly increased in the HBP group and the HFpEF group compared with the control group (P<0.01). There were not significantly different in levels of ACE2 and Ang (1-7) between the HBP group and control group (P>0.05), whereas those levels were significantly increased in the HFpEF group compared with the HBP group and control group (P<0.01). HE staining showed obvious hypertrophy of myocardial cell in the AAC group compared with the sham group. Hypertrophy of myocardial cell in the AAC+Ang (1-7) group was significantly higher than that in the AAC group. Expressions of ACE, ACE2, and Mas receptor proteins were significantly higher in the AAC group than those in the sham group (P<0.05), while the expressions of ACE2 and Mas receptor proteins in the AAC+Ang (1-7) group were significantly higher than those in the AAC group (P<0.05). There was no significant difference in the ACE protein expression between groups (P>0.05).
Conclusion: ACE2 and Ang (1-7) are important predictive factors for the severity of heart failure and myocardial remodeling of HFpEF with hypertension; ACE2-Ang (1-7)-Mas receptor axis may play a protective role in preventing myocardial remodeling in HFpEF with hypertension.
Angiotensin I
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physiology
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Angiotensin II
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Animals
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Atrial Remodeling
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physiology
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Case-Control Studies
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Enzyme-Linked Immunosorbent Assay
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Heart Failure
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metabolism
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physiopathology
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Humans
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Hypertension
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metabolism
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physiopathology
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Male
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Peptide Fragments
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physiology
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Peptidyl-Dipeptidase A
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physiology
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Random Allocation
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Rats
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Rats, Sprague-Dawley
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Receptors, G-Protein-Coupled
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physiology
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Stroke Volume
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Ventricular Function, Left
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physiology
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Ventricular Remodeling
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physiology
4.Development and thinking of new nurses' standardized training in China
Chinese Journal of Modern Nursing 2017;23(5):593-597
Standardized training of the new nurses' is the first step of role adaption for a nursing student to become a nurse. It plays a great role in the development in nursing clinical practice and professional qualities. In recent years,National Health and Family Planning Commission has regarded new nurse standardized training as an important part of nursing talents cultivation. Now,new nurses' standardized training has developed a layered training model. The training contents extends to more aspects,especially in humanistic quality and general skills. Situational teaching and examination become popular in training practice and evaluations which also accept subjective opinions. There are still lacks in dominance of the training system,monitoring and control of process quality,teachers' accreditation and fostering,which need further researches.
5.The relationship between cerebral blood flow velocity and attention and execution function in patients with major depressive episode
Chunfeng HU ; Wu LI ; Longfei LI ; Gang YIN ; Xin ZHANG ; Xiuju WANG
Chinese Journal of Nervous and Mental Diseases 2016;42(11):647-651
Objective To find out the cerebral blood flow velocity and its relationship with attention and execu?tion function in patients with major depressive episode. Methods A total of 70 patients with major depressive episode and 65 healthy controls were included. The 24 items Hamilton depression scale (HAMD-24) was adopted for patients' depressive symptoms assessment. The Cancellation Test (CT) and Wisconsin Card Sorting Test (WCST) were adopted for cognitive function assessment. And the blood flow velocity of cerebral arteries were detected by transcranial Doppler ul?trasonography (TCD). Results Compared with the controls, the patients showed significantly slower average blood flow ve?locity in basilar artery, left middle cerebral artery, right middle cerebral artery, left anterior cerebral artery and right ante?rior cerebral artery (P<0.05). Compared with those in the controls, the net score of each stage and the total net score of CT were significantly lower in the patients, while the total number of responses, response errors, perseverative errors and the necessary response number to complete the first category of WCST were significantly higher (P<0.01). The blood flow velocity in the cerebral basilar artery (r=0.25), left middle cerebral artery (r=0.46), right middle cerebral artery (r=0.25) and right posterior cerebral artery (r=0.26) showed positive correlations with total net score of CT (P<0.05), and the cere?bral artery average blood flow velocity showed negative correlations with the total number of responses, response errors and perseverative errors of WCST in the patients (P<0.05). Conclusions Compared with healthy controls, patients with major depressive episode suffer from lower average cerebral artery blood flow velocity, bad attention and executive func?tion. The change of average cerebral artery blood flow velocity may be responsible for impaired cognitive function in epi?sode major depression patients.
6.Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy.
Xiaoling YANG ; Yuehua ZHANG ; Xiaojing XU ; Xiaoli YU ; Xiuju ZHANG ; Zhixian YANG ; Shuang WANG ; Ye WU ; Xiaoyan LIU ; Xiru WU
Chinese Journal of Pediatrics 2014;52(11):806-811
OBJECTIVETo study the phenotypes and proline-rich transmembrane protein 2 (PRRT2) mutations in families with benign familial infantile epilepsy (BFIE).
METHODData of all BFIE probands and their family members were collected from Peking University First Hospital between September 2006 and August 2013. Clinical phenotypes of affected members were analyzed. Genomic DNA was extracted from peripheral blood samples with standard protocol. Mutations in PRRT2 were screened using PCR amplification and Sanger sequencing.
RESULTTwenty-nine BFIE families were recruited in this study. In total, 110 family members were affected. The age of seizure onset of these affected members was between 2 and 12 months (median: 4.5 months). All probands presented with clusters of seizures. Two probands had one seizure induced by diarrhea respectively at 25 months and 31 months. In four BFIE families, four family members had a history of febrile seizures. PRRT2 mutations were found in 17 of the 29 (58.6%) BFIE families. Mutation c.649_650insC was detected in 12 of the 17 families with PRRT2 mutations. Mutation c.649delC (p.R217EfsX12) was identified in three families. Mutation c.323_324delCA (p. T108SfsX25) and c.904_ 905insG (p. D302GfsX39) were detected in one family, respectively.
CONCLUSIONThe minimum seizure onset age of affected members in BFIE families was 2 months of age. The seizures often occur in clusters. PRRT2 is the major causative gene of BFIE in Chinese families. Mutation c.649_650insC is the hotspot mutation of PRRT2. A novel mutation c.323_324delCA was first reported in BFIE family. Few affected members with PRRT2 mutation presented with febrile seizures phenotype.
Age of Onset ; Asian Continental Ancestry Group ; genetics ; DNA Mutational Analysis ; Epilepsy, Benign Neonatal ; genetics ; Humans ; Infant ; Membrane Proteins ; genetics ; Mutation ; genetics ; Nerve Tissue Proteins ; genetics ; Phenotype ; Seizures ; Seizures, Febrile
7.Clinical features and PRRT2 mutations in infantile convulsions with paroxysmal choreoathetosis.
Xiaoling YANG ; Yuehua ZHANG ; Xiaojing XU ; Shuang WANG ; Zhixian YANG ; Ye WU ; Xiuju ZHANG ; Xiaoyan LIU ; Xiru WU
Chinese Journal of Medical Genetics 2014;31(6):679-685
OBJECTIVETo analyze the phenotypes and proline-rich transmenbrane protein 2 (PRRT2) gene mutations in patients of infantile convulsions with paroxysmal choreoathetosis (ICCA).
METHODSClinical data were collected from ICCA patients and their family members. Genomic DNA was extracted from peripheral blood samples with standard protocol. Mutations of PRRT2 were screened using PCR amplification and Sanger sequencing.
RESULTSEleven families and one sporadic case with ICCA were recruited in this study. In 11 ICCA families, 49 family members were affected, of which 15 individuals had benign infantile convulsions (BIC) alone, 18 individuals had only paroxysmal kinesigenic dyskinesia(PKD), and 16 individuals had BIC followed by PKD. The seizure onset age of infantile convulsions was between 3 and 12 months. The onset age of PKD was ranging from 5 to 17 years old. Four affected members in two ICCA families had PKD or ICCA co-existing with migraine. The one sporadic ICCA case had afebrile seizures between 3.5 and 4 months, and developed paroxysmal twists of limbs after 3 years and 9 months of age. He had good response to treatment with oxcarbazepine at the age of 4 years and 10 months. PRRT2 mutations were identified in all 11 ICCA families. The most common mutation, c.649_650insC (p.R217PfsX8), was detected in 6 of the 11 families (54.5%). PRRT2 mutation (c.649_650insC) was also found in the sporadic ICCA case, and was identified as de novo mutation.
CONCLUSIONThe phenotype of PKD in ICCA families occurred in childhood or adolescence. Few affected members in some ICCA families may have migraine. PRRT2 is the causative gene of ICCA and the mutation c.649_650insC was the hotspot of PRRT2 mutations. PRRT2 mutation was also found in sporadic case with ICCA.
Adolescent ; Adult ; Age of Onset ; Aged ; Aged, 80 and over ; Base Sequence ; Child ; Child, Preschool ; Dyskinesias ; genetics ; Epilepsy, Benign Neonatal ; genetics ; Female ; Humans ; Infant ; Male ; Membrane Proteins ; genetics ; Middle Aged ; Molecular Sequence Data ; Nerve Tissue Proteins ; genetics ; Pedigree ; Phenotype ; Point Mutation ; Seizures ; genetics ; Young Adult
8.Effects of quercetin in combination with bortezomib or lenalidomide on inhibition of proliferation of HL-60 cells
Jie XIAO ; Guomin NIU ; Songmei YIN ; Shuangfeng XIE ; Yiqing LI ; Danian NIE ; Liping MA ; Xiuju WANG ; Yudan WU
The Journal of Practical Medicine 2014;(14):2196-2199
Objective Our preliminary study demonstrates that quercetin can inhibit the proliferation of HL-60 cells. This sudy aimed to find some drugs which could have synergistic effects with quercetin on apoptosis of HL-60 cells. Methods HL-60 cells were cultured with bortezomib at different concentrations (1, 2, 4, 8, 16, and 32μmol/L) alone or combined with quercetin at different concentrations for 48 h. HL-60 cells were cultured with lenalidomide at different concentrations (5, 10, 20, 40, 80, 160, and 320 μmol/L) alone or in combination with quercetin at different concentrations for 48 h. The CCK-8 assay was used to determine the effects on proliferation of HL-60 cells. Results Bortezomib significantly inhibited the proliferation of HL-60 cells (P<0.01). IC50 of quercetin was 49.24μmol/L after cells treated by quercetin combined with bortezomib, which was 13.44μmol/L lower than that treated by quercetin alone. Isobolographic analysis revealed the two drugs had synergistic effect. The results of cell viability of HL-60 cells treated by lenalidomide at lower concentrations (5, 10, 20, 40, and 80μmol/L)were not different from those of the control group (P > 0.05). The results of cell viability of HL-60 cells treated by lenalidomide at higher concentrations (160 and 320μmol/L) were lower than those of the control group (P<0.05). IC50 of quercetin after cells treated by quercetin combined with bortezomib was not different from that treated by quercetin alone. Isobolographic analysis revealed the two drugs had no synergistic effect. Conclusions Bortezomib can inhibit the proliferation of HL-60 cells and it has a synergistic effect with quercetin on HL-60 cells. Lenalidomide has a weaker role in inhibition of the proliferation of HL-60 cells, and it has no synergistic effect with quercetin on HL-60 cells.
9.Effects of membrane-bound prostaglandin E2 synthase 1 inhibitor MK886 on cell cycle of leukemia HL-60/A cells
Yiqing LI ; Songmei YIN ; Liping MA ; Danian NIE ; Shuangfeng XIE ; Xiuju WANG ; Yudan WU
Journal of Leukemia & Lymphoma 2012;21(9):513-516
Objective To investigate the effect of membrane-bound prostaglandin E2 synthase 1 (mPGES-1) inhibitor MK886 on cell cycle of the human acute myeloid leukemia HL-60/A cells.Methods Flow cytometry,Western blot and ELISA were used to measure the difference of cell cycle,expression of cyclin D1, mPGES-1 among HL-60/A cells,MNC and HL-60 cells.The effect of MK886 on cell cycle,cyclin D1,mPGES-1,PGE2,P-Akt and c-myc of HL-60/A cells were observed.Results Compared with MNC and HL-60 cells,the expression of cyclin D1 and mPGES-1 were higher in HL-60/A cells,the percentage of G0-G1 phase was decreased [MNC (62.63±6.58) %,HL-60 (38.86±2.25) %,HL-60/A (30.53±2.15) %]and S phase increased[MNC (12.18±4.43) %,HL-60 (47.70±1.88)%,HL-60/A (57.56±1.54) %](all P< 0.05).After treated with MK886,cell cycle was arrested in G0-G1 phase.The expression of mPGES-1,cyclin D1,P-Akt and c-myc and synthesis of PGE2 were decreased.Conclusion MK886 can arrest HL-60/A cell cycles in G0-G1 phase,which possibly through down-regulation of mPGES-1/PGE2,reduction cyclin D1,P-Akt and c-myc expression.
10.Inhibition effects of the selective COX-2 inhibitor of nimesulide on proliferation of HL-60 leukemia cells
Yiqing LI ; Songmei YIN ; Danian NIE ; Shuangfeng XIE ; Liping MA ; Xiuju WANG ; Yudan WU
Journal of Leukemia & Lymphoma 2010;19(12):735-738
Objectiye To investigate the effect of selective COX-2 inhibitor, nimesulide, on inhibiting proliferation of the human acute myeloid leukemia HL-60 cells. Methods HL-60 cells were treated with different concentration of nimesulide. HL-60 cell proliferation was examined by CCK-8 method. Flow cytometry, Western blotting and ELISA were used to measure the effect of nimesulide on apoptosis, cell cycle,COX-2, PGE2, bax, bcl-2 and c-myc. Results Nimesulide inhibited HL-60 cells proliferation in a dose and time dependence manner. Nimesulide induced cell apoptosis and arrested cell cycle in G0-G1 phase. The expression of COX-2 protein declined after treated with nimesulide 48 h, the total apoptosis in 100, 200,400 μmol/L nimesulide-treated group and control group were (24.97 ± 6.36) %, (34.22 ± 5.76) %, (44.59 ±6.69) % and (4.11 ± 1.26) %, there were significant differences (P < 0.05). Nimesulide inhibited the synthesis of PGE2, the expressions of bcl-2 and c-myc protein and upregulated the expression of bax protein simultaneity.Conclusion Nimesulide significantly inhibited the proliferation of HL-60 cells and induced cell apoptosis,which may be associated with the downregulation of COX-2 expression, reduction of PGE2 synthesis, arrest of cell cycle and regulation bcl-2, c-myc and bax protein expression.

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