天然产物研究与开发
天然產物研究與開髮
천연산물연구여개발
NATURAL PRODUCT RESEARCH AND DEVELOPMENT
2005年
6期
758-761
,共4页
刘绍华%覃青云%方堃%唐献兰%杨卫豪%谢金鲜%李爱媛%周芳%张祥民
劉紹華%覃青雲%方堃%唐獻蘭%楊衛豪%謝金鮮%李愛媛%週芳%張祥民
류소화%담청운%방곤%당헌란%양위호%사금선%리애원%주방%장상민
两面针%镇痛%抗炎%止血%提取物
兩麵針%鎮痛%抗炎%止血%提取物
량면침%진통%항염%지혈%제취물
Zanthoxylum nitidum%analgesia%anti-inflammation%hemostasia%extract
本研究对两面针根的提取物S-O进行了镇痛、止血和抗炎药理实验,每种作用选用两种实验方法来评价.镇痛作用采用热板法和扭体法.热板法实验显示,S-O在150 mg/kg剂量时,小鼠痛阈值明显提高(P<0.01);扭体法实验显示,S-O在150 mg/kg剂量为时,对冰醋酸致痛的小鼠扭体反应次数减少了70.96%(P<0.01).抗炎实验采用二甲苯致小鼠耳廓肿胀法及腹腔染料渗出法.二甲苯致炎剂实验表明,S-O在150 mg/kg剂量时,对二甲苯所致小鼠耳廓肿胀有明显抑制作用,抑制率为63.45%(P<0.01);冰醋酸所致的腹腔毛细血管通透性实验中,S-O在150 mg/kg和75 mg/kg两个剂量组时,对小鼠的抗炎效果分别为52.94%(P<0.01)和52.00%(P<0.01).止血实验采用毛细玻璃管法和载玻片法.毛细玻璃管实验表明S-O在150 mg/kg和75 mg/kg两个剂量时,凝血时间明显缩短(P<0.01);载玻片实验表明S-O在150 mg/kg剂量时,凝血时间明显缩短(P<0.01).总之,两面针中提取物S-O对小鼠具有显著的镇痛、止血和抗炎作用.
本研究對兩麵針根的提取物S-O進行瞭鎮痛、止血和抗炎藥理實驗,每種作用選用兩種實驗方法來評價.鎮痛作用採用熱闆法和扭體法.熱闆法實驗顯示,S-O在150 mg/kg劑量時,小鼠痛閾值明顯提高(P<0.01);扭體法實驗顯示,S-O在150 mg/kg劑量為時,對冰醋痠緻痛的小鼠扭體反應次數減少瞭70.96%(P<0.01).抗炎實驗採用二甲苯緻小鼠耳廓腫脹法及腹腔染料滲齣法.二甲苯緻炎劑實驗錶明,S-O在150 mg/kg劑量時,對二甲苯所緻小鼠耳廓腫脹有明顯抑製作用,抑製率為63.45%(P<0.01);冰醋痠所緻的腹腔毛細血管通透性實驗中,S-O在150 mg/kg和75 mg/kg兩箇劑量組時,對小鼠的抗炎效果分彆為52.94%(P<0.01)和52.00%(P<0.01).止血實驗採用毛細玻璃管法和載玻片法.毛細玻璃管實驗錶明S-O在150 mg/kg和75 mg/kg兩箇劑量時,凝血時間明顯縮短(P<0.01);載玻片實驗錶明S-O在150 mg/kg劑量時,凝血時間明顯縮短(P<0.01).總之,兩麵針中提取物S-O對小鼠具有顯著的鎮痛、止血和抗炎作用.
본연구대량면침근적제취물S-O진행료진통、지혈화항염약리실험,매충작용선용량충실험방법래평개.진통작용채용열판법화뉴체법.열판법실험현시,S-O재150 mg/kg제량시,소서통역치명현제고(P<0.01);뉴체법실험현시,S-O재150 mg/kg제량위시,대빙작산치통적소서뉴체반응차수감소료70.96%(P<0.01).항염실험채용이갑분치소서이곽종창법급복강염료삼출법.이갑분치염제실험표명,S-O재150 mg/kg제량시,대이갑분소치소서이곽종창유명현억제작용,억제솔위63.45%(P<0.01);빙작산소치적복강모세혈관통투성실험중,S-O재150 mg/kg화75 mg/kg량개제량조시,대소서적항염효과분별위52.94%(P<0.01)화52.00%(P<0.01).지혈실험채용모세파리관법화재파편법.모세파리관실험표명S-O재150 mg/kg화75 mg/kg량개제량시,응혈시간명현축단(P<0.01);재파편실험표명S-O재150 mg/kg제량시,응혈시간명현축단(P<0.01).총지,량면침중제취물S-O대소서구유현저적진통、지혈화항염작용.
The roots of Zanthoxylum nitidum(Rox. )DC have been commonly used for rheumatism arthritis,strain gall,neuralgia, toothache, stomach angina, and ulcer etc, in traditional Chinese medicine. This study was performed to assess the efficacies of the extract of the roots of Zanthoxylum nitidum(S-0) on analgesia, anti-inflammation and hemostasia in mice. Each efficacy was assessed by two methods. Analgesia was assessed by the methods of hot-plate and writhing test. In hot plate test, 150 mg/kg S-O has significantly increased the pain threshold of mice( P < 0.01 ). In the writhing test, 150 mg/kg S-O, the number of writhes were reduced more than 70.96% (P < 0.01 ). Anti-inflammation was assessed by the methods of xylene induced ear edema and vascular permeability augmentation by acetic acid test. In the xylene induced ear edema, the inhibition of 150 mg/kg S-O was 63.45 ( P < 0.05). In the vascular permeability augmentation by acetic acid test, the inhibition of anti-inflammation of 150 mg/kg,75 mg/kg S-O were 52.94% ( P <0.05) ,52.00%( P <0.05),respectively,it has significant anti-inflammation.Hemostasia was assessed by the methods of glass tube and glass plate.In glass tube test,both doses of S-O (150 mg/kg, 75 mg/kg) can significantly prolong the blood solidification time ( P < 0.01 ). In the glass plate test, 150 mg/kg S-O can also significantly prolong the blood solidification time( P < 0.01). In conclusion, the S-O of Zanthoxylum nitidum has significant efficacies onanalgesia, anti-inflammation and hemostasia in mice.