Efficacy and safety of isophane protamine insulin injection 30R to isophane protamine biosynthetic human insulin injection 30R in type 2 diabetics poorly controlled with oral hypoglycemic agentsLIAO Huan, SU Qing, JIN Jie, YANG Tao, SHEN Bei, WANG Jian, WANG Yang-tian, CHENG Xing-bo, XIE Yun, SHAN Zhong-yan, et al.
Chinese Journal of Diabetes MellitusVol.03,No.052011
DOI: 10.3760/cma.j.issn.1674-5809.2011.05.006
ObjectiveTo compare the efficacy and safety of isophane insulin injection 30R and isophane protamine biosynthetic human insulin injection 30R in patients with type 2 diabetes mellitus poorly controlled with oral hypoglycemic agents.
MethodsOne hundred and forty patients with type 2 diabetes mellitus poorly controlled with oral hypoglycemic agents from June, 2009 to June, 2010 were divided randomly in a ratio of 1∶1 into group A and group B. There was no differences in age, gender, height, weight between the two groups. The group A and group B were given isophane protamine insulin injection 30R and isophane protamine biosynthetic human insulin injection 30R respectively. All the patients were injected insulin before breakfast and supper together with previous oral agents for 12 weeks. Insulin dosage was determined and adjusted according to blood glucose. At the end of the 12 week, the two groups exchanged the insulins and continued the therapy for another 12 weeks. The glycated hemoglobin A1c(HbA1c), fasting blood glucose(FBG), 2 h postprandial blood glucose (PBG) and insulin autoantibody (IAA) were investigated at the end of the treatments. Paired t test and Wilcoxon test were used in the data analysis.
ResultsAfter 12 weeks, there were no significant differences in HbA1c ((7.7±1.3)% vs (7.5±0.9)%, t=1.24, P>0.05), FBG((8.0±2.0) vs (7.4±1.6)mmol/L,t=1.05, P>0.05) and PBG ((13±4) vs (12±4)mmol/L,t=0.90, P>0.05) in group A and group B. After 24 weeks, no significant differences in the above-mentioned indexes was found between the two groups either: HbA1c ((8.3±1.5)% vs (7.5±1.0)%, χ2=0.01, P>0.05), FBG ((7.8±2.0) vs (7.9±2.1) mmol/L, χ2=0.04, P>0.05) and PBG ((12±4) vs (12±4)mmol/L, χ2=0.82, P>0.05). The levels of IAA were comparable between the two groups at the end of the 12th week ((19±12) vs (19±13) mU/L,t=0.11, P>0.05) and at the end of the 24th week ((19±11) vs (18±12) mU/L, χ2=1.26, P>0.05). The incidence of hypoglycemia in group A was 16.4% before insulin-exchanging and 6.4% after, and that was 15.0% and 2.9% in Group B. No hypersensitivity reaction in local skin, lipoatrophy or subcutaneous nodule occurred during the investigation.
ConclusionThe results suggest that isophane insulin injection 30R has the same efficacy and safety as isophane protamine biosynthetic human insulin injection 30R.
Safety and efficacy of insulin aspart versus regular human insulin in pregnant women with abnormal glucose metabolismLI Nan, YANG Hui-xia, ZHAI Gui-rong, WU Chun-feng
Chinese Journal of Diabetes MellitusVol.03,No.052011
DOI: 10.3760/cma.j.issn.1674-5809.2011.05.007
ObjectiveTo analyze and compare the safety and efficacy of insulin aspart versus regular human insulin in pregnant women with abnormal glucose metabolism.
MethodsIn this study, the data of 77 pregnant women with pre-pregnant diabetes mellitus(DM, n=22) or gestational diabetes mellitus(GDM, n=55) treated from January 2004 to May 2010 with insulin aspart (Asp group) were investigated. And 77 pregnant women with abnormal glucose metabolism using regular human insulin in the mean time were selected as control (HI group) in a ratio of 1∶1. The changes of glucose levels, time for reaching glucose targets, incidence of hypoglycemia and pregnancy outcomes after the treatment were compared between the two groups by using t or rank test.
ResultsOne week of treatment after, the 2 h post-breakfast and post-supper glucose levels in DM women in Asp group were (6.5±1.1) and (7.1±1.1) mmol/L and those were (8.0±1.1) and (7.8±0.8) mmol/L DM women in HI group; the 2 h post-breakfast, post-lunch and post-supper glucose levels in GDM women in Asp group were (6.5±0.7), (6.8±0.7) and (6.7±0.7) mmol/L, and those were (7.1±0.9), (7.3±0.9) and (7.4±0.8) mmol/L in GDM women in HI group. The postprandial glucose levels were all lower in Asp group than those in the HI group (all P<0.05). The time for 2 h post-breakfast glucose level to reach standard in DM women in Asp group was (3.0±2.2) d, and it was (5.0±2.1)d in DM women in HI group; and those were (2.3±1.6) and (4.3±2.6)d in GDM women in Asp group and in HI group, respectively. The time for reaching glucose targets in Asp group were all shorter than those in HI group(P<0.05). The incidence of hypoglycemia in Asp group was 3.9% (1 case of DM and 2 cases of GDM) and it was 24.7% in HI group (8 and 11 cases of DM and GDM, respectively)(P<0.05). The incidence of neonatal hypoglycemia and referral to Pediatrics in DM women in Asp group were 4.5% and 36.4%, and those were 18.2% and 50.0% in DM women in HI group; the prevalence of macrosomia, the neonatal hypoglycemia and referral to Pediatrics in GDM women in Asp group were 10.9%, 3.6% and 25.5%, and those were 18.2%, 10.9% and 38.2% in GDM women in HI group; it seemed that insulin aspart brought more benefits than human insulin, but there was no significant differences between the two groups(allP>0.05).
ConclusionsInsulin aspart is safer and more effective than human insulin when used in pregnant women with DM or GDM; it brings better pregnancy outcomes than human insulin without significant differences.
Relationship between glycemic fluctuation and serum level of connective tissue growth factor in patients with diabetic cardiomyopathyYANG Yu-zhi, XU Li-juan, FENG Kun, WANG Dan, JIANG Hong
Chinese Journal of Diabetes MellitusVol.03,No.052011
DOI: 10.3760/cma.j.issn.1674-5809.2011.05.008
ObjectiveTo investigate the relationship between glycemic fluctuation and serum level of connective tissue growth factor (CTFG) in patients with diabetic cardiomyopathy (DC).
MethodsTwenty healthy controls (male 11, famale 9, aged (40±5) years old) and 50 patients with type 2 diabetes mellitus (T2DM) whose HbA1c were less than 7% were enrolled in this investigation. T2DM patients were further assigned to the non-DC group (n=25, male 13, female 12, aged (41±5) years old) and the DC group (n=25, male 12, female 13, aged (43±6) years old). All the participants underwent continuous glucose monitoring for 3 days to evaluate mean amplitude of glycemic excursion (MAGE) and the absolute mean of daily differences (MODD). Serum CTGF levels were measured by enzyme-linked immunosorbent assay. Analysis of variance and multiple stepwise regression analysis were used for data comparison.
ResultsCTGF levels were significantly increased in DC group ((311±32) ng/L) than in non-DC group ((211±29) ng/L) and normal control group ((181±38) ng/L) (F=81.53, P<0.05). MAGE and MODD in DC group were significantly higher than non-DC group (MAGE: (7.1±1.0) mmol/L vs (6.0±1.0) mmol/L; MODD: (2.56±0.38) mmol/L vs (1.37±0.26) mmol/L;F values were 25.46 and 66.13, respectively; both P<0.05). Serum CTGF levels were positively correlated with 2-h postprandial blood glucose, 24-h urinary albumin, MAGE and MODD (r values were 0.759, 0.655, 0.491 and 0.617, respectively; all P<0.05).
ConclusionsThese findings suggest that increased glycemic fluctuation may play a role in the development of DC. Increased serum CTGF level may be an important factor in the diagnosis and prognosis of DC.
Relationship between donor liver steatosis and post-transplant diabetes mellitus in patients undergoing liver transplantationCHEN Xian-ying, YU Ming-xiang, ZHOU Jian, GAO Jian, GAO Xin
Chinese Journal of Diabetes MellitusVol.03,No.052011
DOI: 10.3760/cma.j.issn.1674-5809.2011.05.009
ObjectiveTo discuss the risk factors of post-transplant diabetes mellitus (PTDM) in patients undergoing liver transplantation, especially donor liver steatosis.
MethodsRetrospectively analyze the data of 438 patients who received orthotopic liver transplantation from April, 2001 to December, 2008. The grade of donor liver steatosis was measured by histopathologic grading of non-alcoholic fatty liver disease in the guideline issued by Chinese Society of Hepatology. The donor liver function was evaluated by Child-Pugh grade system. According to the level of fasting plasma glucose after the operation, the patients were divided into non-PTDM group (n=298, 250 males and 48 females, mean age 48 years) and PTDM group (n=140, 120 males and 20 females, mean age 50 years). Univariate analysis was used to analyze the possible risk factors of PTDM, such as age, gender, fasting plasma glucose, body mass index, liver function before operation, steatosis of donor liver, anti-rejection drug, interleukin-2 receptor antagonist (IL-2RA) use. Multivariate logistic regression was employed based on the univariate analysis.
ResultsThere were 103 cases of donor liver steatosis in 298 non-PTDM patients (34.6%), and 62 donor liver steatosis in 140 PTDM patients (44.3%), no significant differences was found between the two groups(χ2=3.83, P=0.05). Univariate analysis showed that fasting plasma glucose before operation(F=23.38, P<0.05), liver function before operation, the use of IL-2RA and calcineurin inhibitor were significantly related to PTDM(χ2 values was 7.69, 8.30, 0.02, respectively; all P<0.05), but donor liver steatosis was at the critical level in relation to PTDM(χ2=3.83, P=0.05). While multivariate logistic regression indicated abnormal fasting plasma glucose before operation and donor liver steatosis had a positive relation with PTDM, the odds ratio (OR) value was 1.853 (P<0.01) and 1.80 (P<0.05), respectively. And the use of IL-2RA was negatively related with PTDM with aOR value of 0.43 (P<0.01).
ConclusionsAbnormal fasting plasma glucose before operation and donor liver steatosis are risk factors of PTDM, and use of IL-2RA can reduce the risk of PTDM; abnormal liver function before operation may increase the risk of PTDM, while the correlation between calcineurin inhibitor and PTDM needs further study.
Effects of dietary intervention on body weight and insulin sensitivity of patients with polycystic ovary syndromeLI Xin, XIA He-xia
Chinese Journal of Diabetes MellitusVol.03,No.052011
DOI: 10.3760/cma.j.issn.1674-5809.2011.05.010
ObjectiveTo investigate the effects of dietary intervention on body weight and metabolic profiles in patients with polycystic ovary syndrome (PCOS).
MethodsA total of 31 PCOS patients aged 19 to 30 years were assigned to group A (n=17, body mass index (BMI)≥25 kg/m2) or group B (n=14, BMI<25 kg/m2). Anthropometric measurements and hormonal and metabolic profiles were compared in each group before and after the intervention.
ResultsBody weight, BMI and waist circumference of group A were significantly decreased at 1 month (t values were 4.82, 4.79 and 3.32, respectively; all P<0.05), and fasting plasma insulin ((13±6) mU/L vs (21±7) mU/L) and HOMA-IR (0.9±0.5 vs 1.5±0.5) were largely improved (t values were 4.75 and 5.92, respectively; both P<0.01). At 3 months, body weight, BMI and fasting plasma insulin were still decreased (t values were 4.41, 4.28 and 5.92, respectively; all P<0.05). Body weight, BMI and waist circumference of group B were significantly decreased at 1 month (t values were 4.41, 4.28 and 5.14, respectively; all P<0.01), and fasting plasma insulin ((7.1±2.5) mU/L vs (15.2±1.5) mU/L) and HOMA-IR (0.42±0.38 vs 1.16±0.09) were improved (t values were 4.44 and 3.27, respectively; both P<0.05) at 3 months.
ConclusionDietary intervention could improve anthropometric measurements and metabolic profiles in non-obese or obese women with PCOS.
Isolation and purification of islet cells from rhesus monkeysSUN Hui-lin, LIU Hai-ming, ZHANG Zhen, YANG Li, SUN Jia, YANG Rui, CHEN Rong-ping, CHEN Hong, SUN Er-wei, CAI De-hong, et al.
Chinese Journal of Diabetes MellitusVol.03,No.052011
DOI: 10.3760/cma.j.issn.1674-5809.2011.05.011
ObjectiveTo explore a simple and effective method for isolating and purifying rhesus monkeys pancreatic islets.
MethodsThree adult rhesus monkeys were used for this experiment. Pancreas tissue of rhesus monkey was digested with collagenase P by using a semi-automated pancreas-digestion system followed by purification with discontinuous gradients of citrate and puring hyperosmotic solution- Ficoll solution(HCA-Ficoll). After isolation, the islet cell yield and purity was evaluated with light microscope with diphenylthiocarbazne staining, and the islet function was assessed by insulin release assay in vitro. The data were analyzed by using paired t test.
ResultsThe number of the islets collected from each pancreas averaged (101 420±12 054) islet equivalents (IEQ) before and (71 480± 8054) IEQ after purified with discontinuous gradient centrifugation. From each gram of the pancreatic tissue, (2310±252) IEQ were obtained with an average purity of (89.8±8.7)%. The purified islets responded well to high-concentration glucose stimulation(16.7 mmol/L) with a 5.93-fold increase in insulin secretion over the basal level (3.3 mmol/L, t=45.2, P<0.01). The glycemia decreased to normal level after grafted the isolated islets under kidney capsule in diabetic rat.
ConclusionHigh quality islets of rhesus monkeys with good function and shape can be procured by using the method of injecting collagenase into pancreatic duct and the semi-automated pancreas-digestion system followed by purification in a discontinuous gradient of HCA-Ficoll.
Comparison between fluctuated and sustained high glucose on oxidative stress in human retinal pigment epithelial cellsLI Li-qin, SU Sheng-ou, XU Li-li
Chinese Journal of Diabetes MellitusVol.03,No.052011
DOI: 10.3760/cma.j.issn.1674-5809.2011.05.012
ObjectiveTo compare the effects of fluctuated and sustained high glucose on the factor of total superoxide dismutase (SOD) and the levels of malondialdehyde(MDA), glutathione(GSH) in human retinal pigment epithelial cells (HRPE).
MethodsHRPE cells were randomly exposed to seven groups for 72 h: N group(5.5 mmol/L glucose group), H1 group (25 mmol/L of glucose group), H2 group(33 mmol/L of glucose group), F1 group (intermittent exposure for 25 mmol/L and 5.5 mmol/L glucose), F2 group (intermittent exposure for 33 mmol/L and 5.5 mmol/L glucose), P1 group (25 mmol/L of osmotic pressure), P2 group(33 mmol/L of osmotic pressure). The activity of total superoxide(T-SOD), the levels of malondialdehyde(MDA) and glutathione(GSH) were measured. The measurement data of multiple groups were compared with single factor analysis of variance, and the comparison between two groups was performed with LSD test.
Results(1)Compared with N group ((32.1±5.0)mU/L, (135±18)mg/L, (3.3±0.9)mmol/L), the activity of SOD decreased in H1, H2, F1 and F2 groups ((19.9±2.4), (20.5±1.7), (12.8±2.5), (10.9±1.7)mU/L respectively, F=31.56, all P<0.01). The level of GSH decreased in H1, H2, F1 and F2 groups ((97±6), (92±7), (70±7), (71±7)mg/L respectively, F=36.368, all P<0.01). The level of MDA increased in H1, H2, F1 and F2 groups ((13.0±2.0), (11.2±3.3), (17.0±1.4), (19.5±0.5)mmol/L respectively, F=75.642, all P<0.01). The changes were greater in F1 and F2 group (P<0.01). (2)Compared with H1 group, the activity of SOD decreased ((12.8±2.5) vs (19.9±2.4)mU/L, P<0.01), the level of GSH decreased ((69.6±6.7) vs (97.2±6.2)mg/L,P<0.01), the level of MDA increased ((17.0±1.4) vs (13.0±2.0)mmol/L,P<0.01) in F1 group. (3)Compared with H2 group, the activity of SOD decreased ((10.9±1.7) vs (20.5±1.6)mU/L), the level of GSH decreased ((71±7) vs (92±7)mg/L), the level of MDA increased ((19.5±0.5) vs (11.2 ± 3.3)mmol/L, all P<0.01) in F2 group. (4)There was no significant difference between osmotic pressure group and normal glucose group (all P>0.05).
ConclusionFluctuated high glucose may cause a more significant damage to HRPE than the sustained high glucose.
Fosinopril inhibits protein and mRNA expression of thrombospondin-1 in cardiocytes with experimental diabetic ratsWANG Hai-rong, CHEN De-liang, HU Wei, CAO Jian-lei, CHAO Sheng-ping, GAN Xue-dong, ZHANG Lin, XIONG Shi-xi
Chinese Journal of Diabetes MellitusVol.03,No.052011
DOI: 10.3760/cma.j.issn.1674-5809.2011.05.013
ObjectiveTo study the effect of fosinopril on the expression of thrombospondin-1 of cardiomyocytes in experimental diabetic rats.
MethodsA total of 30 SD rats models with diabetes were established by intraperitoneal injection of STZ, and then divided into: diabetes group and fosinopril treatment group. Another 8 healthy rats were set as control group. Collagen typeⅠ, collagen type Ⅲ, transforming growth factor-β1(TGF-β1), angiotensinⅡ, tumor growth factor-β1(TGF-β1) and thrombospondin-1 protein expression were determined by ABC immunohistochemical staining respectively, and the expression of TSP-1 mRNA was determined via RT-PCR. Also we evaluated the expression of TSP-1 in microvascular walls in cardiac.
ResultsCompared with the control group, the expression of collagen typeⅠ(0.36±0.02 vs 0.17±0.02, P<0.05), collagen type Ⅲ(0.35±0.03 vs 0.15±0.02,P<0.05), TGF-β1(0.39±0.04 vs 0.17±0.02, P<0.05), and levels of Ang Ⅱ (11.33±0.97 vs 6.11±0.48,P<0.05)were increased significantly in cardiac interstitial. In addition, TSP-1 was increased significantly in diabetic group when compared to the control group, and fosinopril suppressed these effects(TGF-β1 0.24±0.07 vs 0.49±0.05, P<0.05). But there was no significant difference in expression of TSP-1 in microvascular walls among these groups. The numbers of microvascular walls were decreased in diabetic group, but fosinopril increased the number.TSP-1 mRNA were highly expressed in the diabetic group compare with the control group( 2.01±0.41 vs 0.95±0.01,P<0.05), but fosinopril treatment decreased this high expression (1.02±0.01 vs 2.25±0.21,P<0.05).
ConclusionCompared with the control group, fosinopril inhibited the expression of Collagen typeⅠ, Collagen type Ⅲ, TGF-β1 and TSP-1. Fosinopril decreased the cardiac fibrosis through lowering the levels of Ang Ⅱ and TSP-1, which may suppressed the activity of transformation-β1 and increased the metabolism of cardiomyocytes.
Protective effect of asiatic acid on renal oxidative stress and apoptosis in diabetic ratsCHEN Yan, WU Chen-guang, CHEN Yu-ning, WANG Li, XU Zhi-gang, LI Wen
Chinese Journal of Diabetes MellitusVol.03,No.052011
DOI: 10.3760/cma.j.issn.1674-5809.2011.05.014
ObjectiveTo evaluate the effect of asiatic acid (AA) on renal oxidative stress and apoptosis in streptozotocin (STZ)-induced diabetic rats.
MethodsAfter the diabetic models were successfully established by intraperitoneal injection of 65 μg/g STZ, 24 living SD rats were randomly assigned to 4 groups, including diabetes mellitus group (DM group), 10 μg·g -1·d-1 AA group, 20 μg·g -1·d-1 AA group, and 40 μg·g -1·d-1 AA group. Another 6 healthy SD rats were used as normal controls (NC group). At 8 weeks, urinary albumin excretion rate (UAER), blood glucose (BG), blood urea nitrogen (BUN), serum creatinine (SCr), superoxide dismutase (SOD) activity, and malondialdehvde (MDA) level were tested. Apoptotic cells in the kidneys were observed by TdT-mediated dUTP nick end labeling (TUNEL), the expression of poly-ADP-ribose polymerase (PARP) was detected by immunohistochemistry, and the apoptosis-related protein cystein asperate proteinase-3 (Caspase-3) was tested by Western blot. One-way of variance and LSD t test were used for data analysis.
ResultsCompared with the NC group, the levels of UAER, BG, BUN, SCr, and MDA were significantly increased, the activity of SOD was significantly decreased, and the number of apoptotic cells and the expression of PARP and Caspase-3 were significantly increased in DM group (31.0%±5.5% vs 5.0%±1.2%, 3.9±0.5 vs 1.7±0.6, 1.7±0.4 vs 0.4±0.3, respectively; all P<0.01). Compared with DM group, UAER, BUN and SCr were improved, the activity of SOD was significantly increased, the level of MDA was reduced, and the number of apoptotic cells (DM group: 31.0%±5.5%; 10 μg·g-1·d-1 AA group: 20.6%±4.7%; 20 μg·g -1·d-1 AA group: 15.8%±2.6%; 40 μg·g -1·d-1 AA group: 10.3%±3.3%) and the expressions of PARP (DM group: 3.9±0.5; 10 μg·g -1·d-1 AA group: 3.0±0.2; 20 μg·g -1·d-1 AA group: 2.6±0.4; 40 μg·g -1·d-1 AA group: 2.0±0.3) and apoptosis-related protein Caspase-3 (DM group: 1.7±0.3; 10 μg·g -1·d-1 AA group: 1.0±0.2; 20 μg·g -1·d-1 AA group: 0.7±0.2; 40 μg·g -1·d-1 AA group: 0.5±0.3) were reduced in all 3 AA intervention groups.
ConclusionAA may play a protective role in STZ-induced diabetic nephropathy, which could be related to the inhibition of oxidative stress and apoptosis.
Effects of forkhead transcription factor O1 and piglitazone on glucose consumption of HepG-2 cell lineZHANG Peng-yu, QIN Gui-jun, WANG Shou-jun, ZHANG Ying-hui, MA Xiao-kun, FAN Da-bei
Chinese Journal of Diabetes MellitusVol.03,No.052011
DOI: 10.3760/cma.j.issn.1674-5809.2011.05.015
ObjectiveTo study the effect and mechanism of forkhead transcription factor (FoxO1) and pioglitazone on the glucose utilization in HepG-2 cell line induced by high-level insulin.
MethodsHepG-2 cells were induced by exposure to 1×10-6 mol/L insulin for 24 hours. HepG-2 cells were divided into control group, blank plasmid group, FoxO1 small interfering RNA(siRNA) vector group, and pioglitazone medium group. The blank control group was cultured with normal medium. At 37 ℃, 5% CO2 for 24 hours, the glucose consumption was detected by glucose oxidase method, the expression levels of FoxO1 mRNA and peroxisome proliferator-activated receptors-gamma(PPAR-γ) mRNA were analyzed by RT-PCR, and the protein expression of PPAR-γ was determined by Western blot.Single factor analysis of variance and SNK or Dunnet's test were used for statistic analysis.
ResultsCompared with blank control group, the glucose consumption((1.36 ± 0.03)vs(2.93 ± 0.05)mmol/L, P<0.01), FoxO1 mRNA(0.260±0.025 vs 0.441±0.012,P<0.05)and protein expressions of PPAR-γ decreased(0.312±0.032 vs 0.600±0.046,P<0.05), and the expression of FoxO1 mRNA increased (0.513±0.016 vs 0.425±0.011,P<0.05); there was no difference between FoxO1 siRNA vector group, pioglitazone medium group and blank control group in these indices(P>0.05). After inhibiting FoxO1 by small interference RNA or induced by pioglitazone, these indices were closed to the indices of blank control group. The expressions of FoxO1 mRNA, PPAR-γ mRNA and PPAR-γ protein were highly correlated with the glucose consumption.
ConclusionsInhibiting and increasing the expression of FoxO1 could produce adverse effects on glucose metabolism. Up-regulation PPAR-γ expression could improve insulin sensitivity.