中药新药与临床药理
中藥新藥與臨床藥理
중약신약여림상약리
TRADITIONAL CHINESE DRUG RESEARCH&CLINICAL PHARMACOLOGY
2010年
2期
127-130
,共4页
刘轩%李红艳%夏启胜%徐波%李鸿%贾倞%黄玉堂%李佩文%程志强
劉軒%李紅豔%夏啟勝%徐波%李鴻%賈倞%黃玉堂%李珮文%程誌彊
류헌%리홍염%하계성%서파%리홍%가경%황옥당%리패문%정지강
平肺口服液%人肺成纤维细胞%放射性肺损伤%血清药理学
平肺口服液%人肺成纖維細胞%放射性肺損傷%血清藥理學
평폐구복액%인폐성섬유세포%방사성폐손상%혈청약이학
Pingfei Oral Liquid%Human lung fibroblasts%Radiation-induced lung injury%Serum pharmacology
目的 采用血清药理学方法,研究平肺口服液对人胚肺成纤维细胞增殖及诱导细胞凋亡的作用.方法 平肺口服液10g/kg和20 g/kg分别灌服大鼠,第1~7天每日一次,第8~10天每日两次,于第11天早上末次灌服后2 h腹主动脉无菌采血制备含药血清.采用噻唑蓝(MTT)比色法和流式细胞术分别检测平肺口服液含药血清对人胚肺成纤维细胞(CCC-HPF-1)增殖、细胞凋亡和细胞周期的影响.结果 平肺口服液20 g/kg灌服所得大鼠含药血清作用96 h和120 h分别能抑制CCC-HPF-1细胞增殖(P<0.01);流式细胞术检测表明该含药血清作用96 h能诱导CCC-HPF-1细胞发生凋亡(P<0.05)和G1/G0期阻滞(P<0.05).结论 平肺口服液能抑制肺成纤维细胞增殖,诱导细胞凋亡以及使细胞周期阻滞于G1/G0期,这可能有助于其预防放射性肺损伤.
目的 採用血清藥理學方法,研究平肺口服液對人胚肺成纖維細胞增殖及誘導細胞凋亡的作用.方法 平肺口服液10g/kg和20 g/kg分彆灌服大鼠,第1~7天每日一次,第8~10天每日兩次,于第11天早上末次灌服後2 h腹主動脈無菌採血製備含藥血清.採用噻唑藍(MTT)比色法和流式細胞術分彆檢測平肺口服液含藥血清對人胚肺成纖維細胞(CCC-HPF-1)增殖、細胞凋亡和細胞週期的影響.結果 平肺口服液20 g/kg灌服所得大鼠含藥血清作用96 h和120 h分彆能抑製CCC-HPF-1細胞增殖(P<0.01);流式細胞術檢測錶明該含藥血清作用96 h能誘導CCC-HPF-1細胞髮生凋亡(P<0.05)和G1/G0期阻滯(P<0.05).結論 平肺口服液能抑製肺成纖維細胞增殖,誘導細胞凋亡以及使細胞週期阻滯于G1/G0期,這可能有助于其預防放射性肺損傷.
목적 채용혈청약이학방법,연구평폐구복액대인배폐성섬유세포증식급유도세포조망적작용.방법 평폐구복액10g/kg화20 g/kg분별관복대서,제1~7천매일일차,제8~10천매일량차,우제11천조상말차관복후2 h복주동맥무균채혈제비함약혈청.채용새서람(MTT)비색법화류식세포술분별검측평폐구복액함약혈청대인배폐성섬유세포(CCC-HPF-1)증식、세포조망화세포주기적영향.결과 평폐구복액20 g/kg관복소득대서함약혈청작용96 h화120 h분별능억제CCC-HPF-1세포증식(P<0.01);류식세포술검측표명해함약혈청작용96 h능유도CCC-HPF-1세포발생조망(P<0.05)화G1/G0기조체(P<0.05).결론 평폐구복액능억제폐성섬유세포증식,유도세포조망이급사세포주기조체우G1/G0기,저가능유조우기예방방사성폐손상.
Objective To determine the effects of Pingfei Oral Liquid (PFOL),which is a Traditional Chinese medicine (TCM) prescription, on the growth, apoptosis and cell cycle of human lung fibroblasts. Methods Serum containing PFOL was prepared by serologic pharmacology method . PFOL was administered orally to SD rats at doses of 10 g/kg and 20 g/kg respectively, once a day from the 1st to 7 th day, and twice a day from the 8th to 10th day. Blood was obtained from abdominal aorta aseptically at the 11th day 2 hours after the last morning administration and then the serum was separated. The proliferation of human lung fibroblasts (CCC-HPF-1 )after exposure to the serum was measured by MTT assay. The flow cytometry was used to detect the apoptosis and cell cycle of CCC-HPF-1. Results The growth of CCC-HPF-1 could be suppressed at the 96 h and 120 h after exposure to the serum from rats treated with 20 g/kg PFOL (P < 0.01). The cells were also induced apoptosis (P < 0.05 )and arrested at G1/G0 phase at 96 h after exposure to the serum (P < 0.05). Conclusion PFOL could inhibit proliferation and induce apoptosis of lung fibroblasts, which may contribute to its protective effect on radiation-induced lung injury.