AIM To compare the characteristic of the visual electrophysiology between normal SD rats and a case of abnormal rat with retinal hereditary disease.
目的观察正常SD大鼠和一例患遗传性视网膜疾病大鼠的视觉电生理学特点。
Method: SD rats 30, which were divided into the fast decompression group, HBO exposure group and normal control group.
方法：SD大鼠30只，随机分为快速减压组、高压氧暴露组和正常对照组。
Methods: selected 88 healthy SD male rats, 8 were selected randomly as group a, which was normal group.
方法：将健康的SD雄性大鼠88只随机分为正常对照组(A组，8只)和造模组。
Methods:44 SD rats were divided into the normal group (13 rats) and the osteoporotic model group (31 rats).
方法：SD大鼠44只，随机分为正常组（13只）和骨质疏松模型组（31只）。
Methods The male SD rats were divided into normal group, model group and positive drug group, extract group and remainder group.
方法雄性SD大鼠随机分为正常对照、模型、阳性药、提取物及提取剩余物组。
SD rats were randomly assigned to five groups as follows: saline control group, D-galactose group, DHEA-treated normal group, vehicle control group and DHEA-treated senescent group.
衰老模型实验：SD大鼠随机分为对照组、D-半乳糖组、正常用药组、溶媒对照组和药物治疗组。
MethodsHealthy SD rats 40, half male and half female, were randomly divided into normal group, sham-operated group, model group, electro-acupuncture group.
方法取健康SD大鼠40只，雌雄各半，随机分为正常组、假手术组、模型组、电针组。
Methods 40 healthy male SD rats were randomly divided into the high-fat diet group, the DM control group and the normal group.
方法：40只健康雄性SD大鼠随机分为高脂组、糖尿病对照组、正常组。
METHOD: 144 SD rats were randomly divided into normal groups, experimental control groups and experimental groups.
方法：144只SD大鼠随机分为正常对照组、实验对照组和实验组。
Methods 24, female, SD rats were divided into 3 groups: normal group, end-to-end group, end-to-side group.
方法雌性SD大鼠，共24只，实验分3组，分别为正常对照组、端端缝合组和端侧缝合组。
Abstract: 60 SD rats were randomly divided into normal control group, model control group, Se-enriched Ganoderma lucidum treatment group.
摘要：60只SD大鼠随机分为正常对照组、模型对照组、富硒灵芝治疗组。
Methods SD rats were divided into model group and normal group. CAG model was established according to the related literatures.
方法将SD大鼠随机分为正常对照组和造模组，参照文献制造CAG模型；
Methods The SD rats in normal group were fed with basic forage and in hyperlipemia model group with high fat forage.
方法以喂基础饲料方法建立SD大鼠正常组，以喂高脂饲料方法建立高脂血症大鼠模型。
Methods The SD rats in normal group were fed with basic forage and in hyperlipemia model group with high fat forage.
方法以喂基础饲料方法建立SD大鼠正常组，以喂高脂饲料方法建立高脂血症大鼠模型。
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