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链脲佐菌素诱导的糖尿病对家猪的影响,重点关注氨基酸代谢。

Effects of streptozotocin-induced diabetes in domestic pigs with focus on the amino acid metabolism.

作者信息

Jensen-Waern M, Andersson M, Kruse R, Nilsson B, Larsson R, Korsgren O, Essén-Gustavsson B

机构信息

Department of Clinical Sciences, Section for Comparative Physiology and Medicine, SLU, PO Box 7054, 750 07 Uppsala, Sweden.

出版信息

Lab Anim. 2009 Jul;43(3):249-54. doi: 10.1258/la.2008.008069. Epub 2009 Feb 26.

Abstract

Streptozotocin (STZ) given intravenously destroys pancreatic beta cells and is widely used in animal models to mimic type 1 diabetes. The effects of STZ on the clinical state of health and metabolism were studied in six high health certified domestic pigs weighing 19+/-1.3 kg at the start of the experiment. A single STZ dose of 150 mg/kg of body weight successfully induced hyperglycaemia and alterations in amino acid metabolism. Within 9 h after STZ administration, the blood glucose values fell from 5.4-7.5 mmol/L to 0.8-2.2 mmol/L. Hypoglycaemia was treated with 0.5 g glucose/kg body weight. In all pigs, hyperglycaemia was produced 24 h after STZ treatment, and 3 days after STZ injection, the glucose concentration was >25 mmol/L. Mean C-peptide concentration was 0.25+/-0.16 microg/L since 2 days after STZ injection until the end of the study. The serum concentration of the branched-chain amino acids (BCAA) increased four-fold, and alanine and taurine decreased by approximately 70% and 50%, respectively, after STZ treatment. All but one pig remained brisk and the physical examination was normal except for a retarded growth rate and a reduction of the skeletal muscle. At the end of the study, the pigs were moderately emaciated. Postmortem examination confirmed muscle wasting and a reduction of abdominal and subcutaneous fat. In conclusion, STZ-induced diabetes in pigs fulfils the requirements for a good animal model for type 1 diabetes with respect to clinical signs of the disease and alterations in the carbohydrate and amino acid metabolism.

摘要

静脉注射链脲佐菌素(STZ)可破坏胰腺β细胞,被广泛用于动物模型以模拟1型糖尿病。在实验开始时,对6头经高健康认证、体重为19±1.3千克的家猪研究了STZ对健康和代谢临床状态的影响。150毫克/千克体重的单次STZ剂量成功诱发了高血糖症和氨基酸代谢改变。在给予STZ后9小时内,血糖值从5.4 - 7.5毫摩尔/升降至0.8 - 2.2毫摩尔/升。低血糖症通过给予0.5克葡萄糖/千克体重进行治疗。在所有猪中,STZ治疗后24小时出现高血糖症,STZ注射后3天,血糖浓度>25毫摩尔/升。自STZ注射后2天直至研究结束,平均C肽浓度为0.25±0.16微克/升。STZ治疗后,支链氨基酸(BCAA)的血清浓度增加了四倍,丙氨酸和牛磺酸分别下降了约70%和50%。除一头猪外,所有猪均保持活泼,体格检查正常,但生长速度迟缓且骨骼肌减少。在研究结束时,猪出现中度消瘦。尸检证实有肌肉萎缩以及腹部和皮下脂肪减少。总之,就疾病的临床症状以及碳水化合物和氨基酸代谢的改变而言,STZ诱导的猪糖尿病符合作为1型糖尿病良好动物模型的要求。

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