国际中医中药杂志
國際中醫中藥雜誌
국제중의중약잡지
INTERNATIONAL JOURNAL OF TRIDITIONAL CHINESE MEDICINE
2014年
11期
1013-1016
,共4页
周艳华%张华健%李胜%崔海峰%孙丽华%冯淑怡%于友华%王正品%孙明杰
週豔華%張華健%李勝%崔海峰%孫麗華%馮淑怡%于友華%王正品%孫明傑
주염화%장화건%리성%최해봉%손려화%풍숙이%우우화%왕정품%손명걸
滑膜炎颗粒%止痛药(中药)%疼痛
滑膜炎顆粒%止痛藥(中藥)%疼痛
활막염과립%지통약(중약)%동통
Humoyan Keli%Analgesics(TCD)%Pain
目的:比较滑膜炎颗粒在昆明小鼠和BALB/c小鼠中的镇痛作用。方法80只昆明小鼠、80只BALB/c小鼠各分为对照组、布洛芬组(0.078 g/kg)、滑膜炎颗粒大剂量组(13.98 g/kg)、滑膜炎颗粒中剂量组(6.99 g/kg)、滑膜炎颗粒小剂量组(3.50 g/kg),每组16只,雌雄各半。连续灌胃给药5 d,1次/d。第4天给药后1 h应用鼠尾光照仪,观察鼠尾受热后出现甩尾反应的潜伏期。末次给药后1 h腹腔注射醋酸制备疼痛模型,观察小鼠扭体潜伏期及扭体次数。结果滑膜炎颗粒各剂量组对昆明小鼠痛阈潜伏期、扭体次数无明显影响,滑膜炎颗粒中剂量组可减少雄性BALB/c小鼠痛阈潜伏期(3.93±0.76)min,与对照组的(4.84±1.16)min 比较,差异有统计学意义(P<0.05)。滑膜炎颗粒小、中、大剂量组均能减少BALB/c小鼠扭体次数[分别为(8.56±6.19)次、(5.73±3.17)次、(6.88±4.59)次],与对照组的(19.06±6.34)次比较,差异有统计学意义(P<0.01)。结论滑膜炎颗粒各剂量组对化学刺激所致疼痛呈较好镇痛作用,镇痛作用无性别差异;昆明小鼠个体差异较大,不适宜镇痛药的药效学评价,应选用个体差异小的BALB/c小鼠制备疼痛动物模型。
目的:比較滑膜炎顆粒在昆明小鼠和BALB/c小鼠中的鎮痛作用。方法80隻昆明小鼠、80隻BALB/c小鼠各分為對照組、佈洛芬組(0.078 g/kg)、滑膜炎顆粒大劑量組(13.98 g/kg)、滑膜炎顆粒中劑量組(6.99 g/kg)、滑膜炎顆粒小劑量組(3.50 g/kg),每組16隻,雌雄各半。連續灌胃給藥5 d,1次/d。第4天給藥後1 h應用鼠尾光照儀,觀察鼠尾受熱後齣現甩尾反應的潛伏期。末次給藥後1 h腹腔註射醋痠製備疼痛模型,觀察小鼠扭體潛伏期及扭體次數。結果滑膜炎顆粒各劑量組對昆明小鼠痛閾潛伏期、扭體次數無明顯影響,滑膜炎顆粒中劑量組可減少雄性BALB/c小鼠痛閾潛伏期(3.93±0.76)min,與對照組的(4.84±1.16)min 比較,差異有統計學意義(P<0.05)。滑膜炎顆粒小、中、大劑量組均能減少BALB/c小鼠扭體次數[分彆為(8.56±6.19)次、(5.73±3.17)次、(6.88±4.59)次],與對照組的(19.06±6.34)次比較,差異有統計學意義(P<0.01)。結論滑膜炎顆粒各劑量組對化學刺激所緻疼痛呈較好鎮痛作用,鎮痛作用無性彆差異;昆明小鼠箇體差異較大,不適宜鎮痛藥的藥效學評價,應選用箇體差異小的BALB/c小鼠製備疼痛動物模型。
목적:비교활막염과립재곤명소서화BALB/c소서중적진통작용。방법80지곤명소서、80지BALB/c소서각분위대조조、포락분조(0.078 g/kg)、활막염과립대제량조(13.98 g/kg)、활막염과립중제량조(6.99 g/kg)、활막염과립소제량조(3.50 g/kg),매조16지,자웅각반。련속관위급약5 d,1차/d。제4천급약후1 h응용서미광조의,관찰서미수열후출현솔미반응적잠복기。말차급약후1 h복강주사작산제비동통모형,관찰소서뉴체잠복기급뉴체차수。결과활막염과립각제량조대곤명소서통역잠복기、뉴체차수무명현영향,활막염과립중제량조가감소웅성BALB/c소서통역잠복기(3.93±0.76)min,여대조조적(4.84±1.16)min 비교,차이유통계학의의(P<0.05)。활막염과립소、중、대제량조균능감소BALB/c소서뉴체차수[분별위(8.56±6.19)차、(5.73±3.17)차、(6.88±4.59)차],여대조조적(19.06±6.34)차비교,차이유통계학의의(P<0.01)。결론활막염과립각제량조대화학자격소치동통정교호진통작용,진통작용무성별차이;곤명소서개체차이교대,불괄의진통약적약효학평개,응선용개체차이소적BALB/c소서제비동통동물모형。
Objective To compare the analgesic effect ofHuamoyan Keli(HMYKL) between Kunming mice and BALB/c mice.Methods Eighty Kunming mice and eighty BALB/c mice were randomly divided into five groups, respectively: a control group, a ibuprofen group, a HMYKL high-dose group(13.98 g crude dru g/kg), HMYKL middle-dose group(6.99 g crude drug/kg)and a HMYKL low-dose group(3.50 g crude dru g/kg). There were 16 mice in each group with 8 male mice and 8 female mice. Drugs were administered intragastrically daily for 5 days. After 1 h of drug treatment on day 4, the latency of tail-flick response was evaluated using illuminated pain measurement instrument. After the last drug treatment, pain model was established by i.p. acetic acid, writhing latency and writhing times were recorded to evaluate the analgesic effect of HMYKL.Results In tail-flick test, there was no statistical difference among male and female Kunming mice in the HMYKL groups. Among male BALB/c mice, the latency in HMYKL middle-dose group was significantly longer than that in the control group(4.84±1.16 minvs. 3.93±0.76 min,P<0.05). In writhing test, compared with control group(19.06±6.34), the writhing times among BALB/c mice were decreased in HMYKL high-dose group(8.56±6.19), HMYKL middle-dose group(5.73±3.17), HMYKL low-dose group(6.88±4.59)(allP<0.01).Conclusion All dose groups of HMYKL showed good analgesic effect on the pain induced by chemical stimulation and there was no sex difference. Kunming mice were not suitable for the evaluation of the analgesic pharmacodynamics because of their large individual difference. On contrast, BALB/c mice which had less individual difference could be used to produce the model of pain.