PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 30317639-0 2019 Proinsulin C-peptide as an alternative or combined treatment with insulin for management of testicular dysfunction and fertility impairments in streptozotocin-induced type 1 diabetic male rats. Streptozocin 144-158 insulin 2 Rattus norvegicus 11-20 31669668-10 2020 The methanol extract of the plant prevented the diabetogenic effect of STZ and significantly lowered the fasting blood glucose level, glycated haemoglobin and increased insulin and C-peptide level in treated rats. Streptozocin 71-74 insulin 2 Rattus norvegicus 181-190 28991371-3 2018 They increased the concentrations of serum insulin, C-peptide and Glp-1 (P < 0.05) by improving the STZ-induced damage of islet beta-cells and increasing their insulin expression (P < 0.05). Streptozocin 103-106 insulin 2 Rattus norvegicus 52-61 30408473-5 2019 Combined treatment of HFD and STZ (20 mg/kg) in the DCRD manner were significantly induced late-stage diabetic complication with sustained hyperglycaemia, no mortality, increased HbA1c and dyslipidaemia, reduced insulin, C-peptide and beta cells. Streptozocin 30-33 insulin 2 Rattus norvegicus 221-230 31185481-3 2019 METHODS: Rats were either injected once with 65 mg/kg streptozotocin (STZ) before being sacrificed after 8 weeks or were treated with a daily injection of insulin 2 days by STZ and continued until being sacrificed. Streptozocin 173-176 insulin 2 Rattus norvegicus 155-164 29517782-5 2018 The RCE treatment lowered blood glucose, and glycated and fetal hemoglobin concentrations and improved glucose tolerance as well as considerably raised serum insulin, proinsulin and C-peptide levels in streptozotocin-treated rats. Streptozocin 202-216 insulin 2 Rattus norvegicus 182-191 23105684-1 2007 The objective of this study is to induce experimental diabetes mellitus by Streptozotocin in normal adult Wistar rats via comparison of changes in body weight, consumption of food and water, volume of urine and levels of glucose, insulin and C-peptide in serum, between normal and diabetic rats. Streptozocin 75-89 insulin 2 Rattus norvegicus 242-251 25560570-4 2015 RESULTS: STZ-induced diabetes was associated with body weight reduction, hyperglycemia, overproduction of glycated hemoglobin, as well as decline in serum insulin, C-peptide, and insulin like growth factor-I. Streptozocin 9-12 insulin 2 Rattus norvegicus 164-207 25298622-1 2014 The objective of this study is to induce experimental diabetes mellitus by streptozotocin in normal adult Wistar rats via comparison of changes in body weight, consumption of food, volume of water, urine and levels of glucose, insulin and C-peptide in serum, between normal and diabetic rats. Streptozocin 75-89 insulin 2 Rattus norvegicus 239-248 21618400-3 2011 METHODS: The effect of C-peptide incubation (2 h) on gene expression was investigated in freshly isolated proximal tubular cells from streptozotocin-diabetic Sprague-Dawley rats using global gene expression profiling and real-time quantitative polymerase chain reaction. Streptozocin 134-148 insulin 2 Rattus norvegicus 23-32 21106770-10 2010 In conclusion, C-peptide administration to STZ-diabetic rats for 8 weeks results in the inhibition of diabetes-induced expansion of the mesangial matrix. Streptozocin 43-46 insulin 2 Rattus norvegicus 15-24 16799398-14 2006 CONCLUSIONS: C-peptide administration in replacement dose to streptozotocin diabetic rats induces weight gain regardless hyperglycaemia or glycosuria. Streptozocin 61-75 insulin 2 Rattus norvegicus 13-22 17103462-0 2007 The C-peptide fragment EVARQ reduces glomerular hyperfiltration in streptozotocin-induced diabetic rats. Streptozocin 67-81 insulin 2 Rattus norvegicus 4-13 12525088-4 2001 The results showed that: (1) blood glucose of STZ diabetic rats was higher, serum insulin, C-peptide and leptin level were lower than that of normal rats; (2) blood glucose was decreased, and blood insulin and C-peptide were increased in exercised STZ diabetic group. Streptozocin 46-49 insulin 2 Rattus norvegicus 210-219 8800366-0 1996 Effect of C-peptide administration on whole body glucose utilization in STZ-induced diabetic rats. Streptozocin 72-75 insulin 2 Rattus norvegicus 10-19 8800366-8 1996 These results thus demonstrate that C-peptide has the capacity to increase glucose utilization in STZ-induced diabetic rats. Streptozocin 98-101 insulin 2 Rattus norvegicus 36-45 16101290-3 2005 Here we show that chemically synthesized INS2 has biological activity that significantly enhances insulin reduction of hyperglycemia in streptozotocin diabetic rats. Streptozocin 136-150 insulin 2 Rattus norvegicus 41-45 2973549-3 1988 The pups born to the streptozotocin-treated mothers had higher birth weight, pancreatic insulin content, plasma insulin, and C-peptide concentrations compared with pups born to control mothers. Streptozocin 21-35 insulin 2 Rattus norvegicus 77-134