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小檗碱单独及与1,3-双(2-氯乙基)-1-亚硝基脲联合用于治疗恶性脑肿瘤的实验室研究。

Laboratory studies of berberine used alone and in combination with 1,3-bis(2-chloroethyl)-1-nitrosourea to treat malignant brain tumors.

作者信息

Zhang R X, Dougherty D V, Rosenblum M L

机构信息

Department of Neurosurgery, Second Affiliated Hospital, Hebei Medical College, Shijiazhuang.

出版信息

Chin Med J (Engl). 1990 Aug;103(8):658-65.

PMID:2122945
Abstract

Berberine was evaluated for antitumor activity against malignant brain tumors. In addition, studies on combination of berberine with 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) were done. Several experimental approaches were used. In vitro studies were performed on a series of 6 human malignant brain tumor cell lines and rat 9L brain tumor cells (gliosarcoma) by using a colony forming efficiency (CFE) assay. 9L was also evaluated by a sister chromatid exchange (SCE) assay. In addition, in vivo treatment of intracerebral 9L solid brain tumors was analyzed by CFE assay. Berberine used alone at a dose of 150 micrograms/ml showed an average of 91% cell kill (1.08 log kill) for the 6 malignant brain tumor cell lines. On the average, BCNU alone at a dose of 23 microM gave a 43% cell kill (0.24 log kill). Treatment with a combination of berberine and BCNU at 23 microM showed additive effects with an average of 97% cell kill (1.55 log kill). The relative number of SCEs for 9L cells was increased 2.7 times over background following in vitro treatment with 150 micrograms/ml berberine. Following in vivo treatment of animals harboring solid 9L brain tumors with 10 mg/kg of berberine, an 80.9% cell kill (0.69 log kill) was noted. This activity is equivalent to treatment with 1/3 LD10 dose of BCNU (4.44 mg/kg). In vivo combination treatment with berberine and BCNU showed additive cytotoxicity. Using a BCNU-resistant 9L subline (9L-2), treatment with berberine in combination with BCNU also demonstrated additive cytotoxicity. In conclusion, our results indicate that berberine has potent antitumor activity against human and rat malignant brain tumors.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对小檗碱针对恶性脑肿瘤的抗肿瘤活性进行了评估。此外,还开展了小檗碱与1,3-双(2-氯乙基)-1-亚硝基脲(卡莫司汀,BCNU)联合使用的研究。采用了多种实验方法。通过集落形成效率(CFE)试验,对一系列6种人类恶性脑肿瘤细胞系和大鼠9L脑肿瘤细胞(胶质肉瘤)进行了体外研究。还通过姐妹染色单体交换(SCE)试验对9L细胞进行了评估。此外,通过CFE试验分析了对脑内9L实体脑肿瘤的体内治疗情况。单独使用剂量为150微克/毫升的小檗碱时,对6种恶性脑肿瘤细胞系平均显示出91%的细胞杀伤率(1.08对数杀伤)。平均而言,单独使用剂量为23微摩尔的BCNU时,细胞杀伤率为43%(0.24对数杀伤)。小檗碱与23微摩尔的BCNU联合治疗显示出相加效应,平均细胞杀伤率为97%(1.55对数杀伤)。用150微克/毫升小檗碱体外处理后,9L细胞的SCE相对数量比背景增加了2.7倍。用10毫克/千克小檗碱对患有实体9L脑肿瘤的动物进行体内治疗后,观察到细胞杀伤率为80.9%(0.69对数杀伤)。该活性等同于用1/3 LD10剂量的BCNU(4.44毫克/千克)进行治疗。小檗碱与BCNU的体内联合治疗显示出相加的细胞毒性。使用对BCNU耐药的9L亚系(9L-2)时,小檗碱与BCNU联合治疗也显示出相加的细胞毒性。总之,我们的结果表明,小檗碱对人类和大鼠恶性脑肿瘤具有强大的抗肿瘤活性。(摘要截短为250字)

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