The diabetic rat model was induced by STZ.
糖尿病大鼠模型用链脲佐菌素（STZ）腹腔注射诱导。
Methods Diabetes was induced by injecting STZ.
方法链尿佐菌素(STZ)诱发大鼠糖尿病。
METHOD Models were made with high-fat diet and STZ injection.
方法以高脂饲养结合STZ腹腔注射造模。
Methods The diabetic rat model was established by streptozotocin (STZ).
方法以链脲佐菌素(STZ)诱发糖尿病模型。
Objective: to observe Tangshen Fuyuan decoctions effect on DN rats due to STZ.
目的：观察糖肾复元汤对链脲霉素(STZ)糖尿病肾病大鼠的疗效。
DiscussionThe STZ rat model is used commonly experimental diabetic ani-mal model.
STZ大鼠模型是普遍采用的实验性糖尿病动物模型。
Objective: to observe the effect of Fu-spleen decoction on the SOD and LPO of STZ rats.
目的：观察复脾汤对STZ大鼠血糖、超氧化物歧化酶（SOD）、过氧化脂质（LPO）等指标的影响。
METHODS Established rat model of diabetes mellitus by intraperitoneal injection of STZ.
方法经大鼠腹腔注射STZ制备糖尿病大鼠模型。
Results (1) The blood glucose increased and blood insulin decreased in STZ diabetic group.
结果（1）糖尿病大鼠血糖浓度增高，血胰岛素浓度降低；
Methods SD rat model of diabetes was established by intraperitoneal injection of streptozotocin (STZ).
方法链脲佐菌素(STZ)单次腹腔注射制作SD大鼠糖尿病模型。
The diabetic rats models were induced by the single injection of streptozotocin (STZ) via coccygeal vein.
由尾静脉单次注射链脲佐菌素(STZ)，造成糖尿病大鼠模型。
Methods Rabbit models with type 2 diabetes were induced by intravenous injection of streptozotocin (STZ).
方法通过静脉注射致病剂量链脲左菌素（STZ），诱发兔高血糖，制备2型糖尿病兔模型；
Type 2 fat diabetic rat model was built by injection with streptozotocin (STZ) and intake of high lipid diet.
腹腔注射链脲霉素及饲喂高脂日粮，建立2型糖尿病大鼠模型。
Objective: To study the effect of compound of Tang Ping Jian Herbs on metabolism of STZ-induced diabetic rats.
目的：研究糖平煎复方对糖尿病大鼠代谢的影响。
The recombinant protein could significantly reduce the level of blood glucose in STZ-induced hyperglycemia model.
该重组蛋白能够降低STZ诱导的小鼠高血糖模型的血糖水平。
AIM: to explore the protective effects of riboflavin on the kidney in streptozotocin (STZ) -induced diabetic rats.
目的：探讨核黄素对STZ诱导的大鼠糖尿病肾病的治疗作用及机制。
Objective: To observe the effect of compound of sour medicinal herbs (CSMH) on metabolism of STZ induced diabetic rat.
目的：研究酸味中药复方对糖尿病大鼠代谢的影响。
Conclusion:Rat IDDM model induced by mutiple injection low dose of STZ is an ideal animal model to investigate diabetes.
结论：STZ小剂量多次注射诱导大鼠胰岛素依赖性糖尿病（IDDM）动物模型适用于糖尿病发病机理的研究。
Objective: To study the preventive effect of bovine colostrum powder (BCP) on hyperglycemia in STZ-induced diabetic rats.
目的：探讨牛初乳粉(BCP)对大鼠糖尿病的预防作用。
Rats in DN group and TWP group were given streptozocin (STZ) by intraperitoneal injection to establish animal model of diabetes.
糖尿病组与TWP治疗组大鼠分别给予链脲菌素(STZ)一次性腹腔注射建立糖尿病大鼠模型。
Methods Rat models of type 2 diabetes and fatty liver were established by injecting small doses of STZ and feeding high fat fodder.
方法采用小剂量链脲佐菌素(STZ)腹腔注射加高脂饲料喂养方法，建立2型糖尿病并脂肪肝动物模型。
First successfully use of STZ diabetic rat model, and then use ligation of the left hind limb iliac artery get the DLASO rat model.
首先采用STZ成功造模糖尿病大鼠，然后结扎大鼠左后肢髂外动脉，造成大鼠dlaso模型。
The main purpose of the passage is to evaluate the cost of making STZ-induced diabetic rat models by establishing a mathematic model.
通过建立数学模型描述制作糖尿病大鼠模型的成本。
Objective: to validate the reliability of type 2 diabetes rat model induced by streptozotocin (STZ) plus high calorie and high sugar diet.
目的：验证链脲佐菌素(STZ)加高脂高糖饲料诱导的2型糖尿病大鼠模型的可靠性。
Objective: To investigate the hypoglycemic and hypolipidemic effects of Ganoderma Polysaccharide in rats with STZ-induced type 2 diabetes.
目的：研究灵芝多糖对链脲佐菌素诱导的2型糖尿病大鼠降糖降脂作用。
Objective: To observe the effect of compound of sour medicinal herbs (CSMH) on glomerular pathological changes in STZ induced diabetic rat.
目的：探讨酸味中药复方对糖尿病大鼠肾小球病变的影响。
Conclusion: GSPE can inhibit nonenzymatic reactions of glycosylation in STZ-induced diabetic rats and protect the myocardial ultra-structure.
结论：GSPE能够抑制STZ糖尿病大鼠非酶糖基化反应，对其心脏超微结构有一定保护作用。
Methods Diabetic nephropathy rats were induced by excision of the right kidney and a single intraperitoneal injection of streptozotocin (STZ).
方法采用右肾切除加腹腔一次性注射链脲佐菌素建立糖尿病肾病动物模型。
Methods Steptozotocin (STZ) induced and sucrose induced diabetic rats were employed as DCP and diuresis models. Normal rats served as the control.
方法分别以链脲佐菌素(STZ)、蔗糖诱导制作大鼠dcp模型及利尿模型，正常大鼠作对照。
Conclusion Rosiglitazone can reduce STZ-induced nerve cell toxicity, to improve cell survival, though its mechanism still need to be further explored.
结论罗格列酮可以减轻STZ引起的神经细胞毒性，提高细胞生存率，其作用机制尚需进一步探讨。
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