The analgesic effects were assessed by hot-plate test in mice and twisting response induced by ethanoic acid in mice.
通过热板试验对小鼠的镇痛作用进行评价，并通过乙酸对小鼠的扭转反应进行评价。
Methods: The hot plate test in mice and tail stimulation vocalization test in rats were used.
方法： 用热板法和电刺激嘶叫法分别测定小鼠和大鼠的痛阈。
Methods Writhing test, hot plate and thrilling test in mice were applied.
方法采用小鼠扭体、热板、甩尾等疼痛模型。
Methods Writhing and hot plate tests in mice, model tests on pylorus ligatured gastric ulcer gastric ulcer by acetic acid induced in rats and external test on pepsin activity, were used in this study.
方法采用小鼠扭体法、热板法，大鼠幽门结扎性胃溃疡模性，醋酸烧灼性胃溃疡模型以及体外胃蛋白酶活性实验进行观察。
METHODS The analgesic effects were studied by writhing, hot plate test in mice and electric stimulation test in rats.
方法：采用小鼠扭体法、小鼠热板法、大鼠电刺激鼠尾法进行镇痛实验。
METHODS the writhing model of mice induced by acetic acid, hot plate test (sc, icv), tail flick test and the model of electrical stimulation induced contraction of guinea pig ileum were used.
方法通过醋酸扭体模型、热板、甩尾、纳洛酮拮抗试验及豚鼠回肠离体标本研究样品的镇痛活性及机制。
Method Hot Plate test in mice.
方法：小鼠热板法。
Methods of acetic acid induced writhing and hot plate test in mice were used to study the analgesic effect.
用小鼠醋酸扭体法和热板法，观察绿舒筋多糖的镇痛作用。
Methods: The analgesic effects were assessed by hot-plate test in mice and twisting response induced by ethanoic acid in mice.
方法：采用冰醋酸扭体法和热板法对小鼠进行镇痛试验；采用二甲苯耳肿法和角叉菜胶足跖肿胀法对小鼠进行抗炎试验。
Methods: Through the mice hot plate test and tail pain tenderness test, compared to the control group and the positive drug Voltaren group to study the drug's analgesic effect.
方法：通过对小鼠进行热板法镇痛实验及鼠尾压痛实验，对比空白组及阳性药物扶他林组，以研究该药的镇痛作用。
The writhing induced by acetic acid and the pain caused by formaldehyde were inhibited significantly, but the pain threshold was enhanced by GQ only at high dose in hot-plate test in mice.
GQ显著抑制小鼠醋酸诱导的扭体反应和甲醛性疼痛，大剂量时，能提高小鼠热板痛阈值。
The writhing induced by acetic acid and the pain caused by formaldehyde were inhibited significantly, but the pain threshold was enhanced by GQ only at high dose in hot-plate test in mice.
GQ显著抑制小鼠醋酸诱导的扭体反应和甲醛性疼痛，大剂量时，能提高小鼠热板痛阈值。
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