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比格犬脑室内注射二氟甲基鸟氨酸(DFMO)和甲基乙二醛双脒腙(MGBG)后的中枢神经系统毒性及脑脊液药代动力学

CNS toxicity and CSF pharmacokinetics of intraventricular DFMO and MGBG in beagle dogs.

作者信息

Levin V A, Byrd D, Campbell J, Davis R L, Borcich J K

出版信息

Cancer Chemother Pharmacol. 1984;13(3):200-5. doi: 10.1007/BF00269029.

Abstract

We have developed a beagle dog model to study the pharmacology and toxicology of anticancer drugs administered through the 3rd or lateral ventricles. A Foltz-type reservoir was implanted SC and connected by tube into a cerebral ventricle. Drugs were administered directly into the reservoir; CSF sampling of drugs administered into the ventricle was achieved directly by tapping the reservoir or by percutaneous puncture of the cisterna magna. In the current study, we evaluated the CSF pharmacokinetics and CNS toxicity of two inhibitors of polyamine metabolism, alpha-difluoromethylornitine (DFMO) and methylglyoxal bisguanylhydrazone (MGBG). Both drugs were judged too toxic to justify intrathecal or intraventricular studies with these agents in patients.

摘要

我们开发了一种比格犬模型,用于研究通过第三脑室或侧脑室给药的抗癌药物的药理学和毒理学。将一个福尔茨型贮器皮下植入,并通过导管连接到脑室。药物直接注入贮器;通过轻敲贮器或经皮穿刺枕大池直接获取注入脑室内药物的脑脊液样本。在本研究中,我们评估了两种多胺代谢抑制剂α-二氟甲基鸟氨酸(DFMO)和甲基乙二醛双脒腙(MGBG)的脑脊液药代动力学和中枢神经系统毒性。这两种药物被判定毒性太大,无法在患者中对这些药物进行鞘内或脑室内研究。

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