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用于脑室内或鞘内给药及颅内压长期研究的灵长类动物模型。

Primate model for long-term study of intraventricularly or intrathecally administered drugs and intracranial pressure.

作者信息

Wood J H, Poplack D G, Bleyer W A, Ommaya A K

出版信息

Science. 1977 Feb 4;195(4277):499-501. doi: 10.1126/science.402027.

DOI:10.1126/science.402027
PMID:402027
Abstract

Meaningful pharmacokinetic investigations require animal systems which approximate the human situation. This report describes a primate model in which silicone catheters are placed into the fourth ventricle and the spinal subarachnoid space and connected to subcutaneous cerebrospinal fluid without tissue damage, prod, enables spinoventricular perfusion, and permits ventricular cerebrospinal fluid sampling over extended periods in unanethetized rhesus monkeys. This animal system may provide intraventricular pressure recordings and pharmacokinetic data similar to that obtained in man.

摘要

有意义的药代动力学研究需要近似人类情况的动物系统。本报告描述了一种灵长类动物模型,其中硅胶导管被置入第四脑室和脊髓蛛网膜下腔,并与皮下脑脊液相连,无组织损伤,可实现脊髓脑室灌注,并允许在未麻醉的恒河猴中长时间采集脑室脑脊液样本。这种动物系统可能提供与人类相似的脑室内压力记录和药代动力学数据。

相似文献

1
Primate model for long-term study of intraventricularly or intrathecally administered drugs and intracranial pressure.用于脑室内或鞘内给药及颅内压长期研究的灵长类动物模型。
Science. 1977 Feb 4;195(4277):499-501. doi: 10.1126/science.402027.
2
Chronic ventricular cerebrospinal fluid sampling, drug injections, and pressure monitoring using subcutaneous reservoirs in monkeys.在猴子身上使用皮下储液器进行慢性脑室脑脊液采样、药物注射和压力监测。
Neurosurgery. 1977 Sep-Oct;1(2):132-5. doi: 10.1227/00006123-197709000-00009.
3
Cerebral subarachnoid sampling of cerebrospinal fluid in the rhesus monkey.恒河猴脑脊液的脑蛛网膜下腔采样
Lab Anim Sci. 1994 Apr;44(2):148-52.
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Kinetics of elimination of methotrexate from the cerebrospinal fluid space of monkeys after ventriculolumbar perfusion.经脑室-腰椎灌注后甲氨蝶呤从猴脑脊液空间消除的动力学
Cancer Treat Rep. 1977 Jul;61(4):603-11.
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Methotrexate distribution within the subarachnoid space after intraventricular and intravenous administration.甲氨蝶呤经脑室内和静脉内给药后在蛛网膜下腔内的分布。
Cancer Chemother Pharmacol. 2000;45(3):259-64. doi: 10.1007/s002800050038.
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A primate model for study of methotrexate pharmacokinetics in the central nervous system.用于研究甲氨蝶呤在中枢神经系统中药代动力学的灵长类动物模型。
Cancer Res. 1977 Jul;37(7 Pt 1):1982-5.
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Supratentorial pressures. Part I: Differential intracranial pressures.幕上压力。第一部分:颅内压差
Neurol Res. 1987 Sep;9(3):193-7. doi: 10.1080/01616412.1987.11739794.
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A rhesus monkey model for continuous infusion of drugs into cerebrospinal fluid.一种用于向脑脊液中持续输注药物的恒河猴模型。
Lab Anim Sci. 1990 Sep;40(5):520-5.
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Distribution of methotrexate in the cerebrospinal fluid and brain after intraventricular administration.脑室内给药后甲氨蝶呤在脑脊液和脑内的分布。
Cancer Treat Rep. 1977 Jul;61(4):633-41.
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Physiological pressure variations within the cerebrospinal fluid pathways in man.人类脑脊液通路中的生理压力变化。
J Physiol. 1968 May;196(2):136P-137P.

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Plasma and cerebrospinal fluid pharmacokinetics of vincristine and vincristine sulfate liposomes injection (VSLI, marqibo®) after intravenous administration in Non-human primates.非人类灵长类动物静脉注射长春新碱及硫酸长春新碱脂质体注射液(VSLI,marqibo®)后的血浆和脑脊液药代动力学
Invest New Drugs. 2016 Feb;34(1):61-5. doi: 10.1007/s10637-015-0311-x. Epub 2015 Dec 10.
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Comp Med. 2015 Feb;65(1):77-82.
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Pharmacokinetics following intraventricular administration of chemotherapy in patients with neoplastic meningitis.肿瘤性脑膜炎患者脑室内给予化疗后的药代动力学。
Clin Pharmacokinet. 2005;44(1):1-31. doi: 10.2165/00003088-200544010-00001.
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Pharmacokinetic study of cerebrospinal fluid penetration of cis-diamminedichloroplatinum (II).顺二氯二氨铂(II)脑脊液穿透的药代动力学研究
Cancer Chemother Pharmacol. 1981;5(4):257-60. doi: 10.1007/BF00434394.
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Penetration of SCH-39304, a new antifungal triazole, into cerebrospinal fluid of primates.新型抗真菌三唑类药物SCH-39304在灵长类动物脑脊液中的渗透情况。
Antimicrob Agents Chemother. 1990 Jun;34(6):1281-4. doi: 10.1128/AAC.34.6.1281.
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Current pharmacological treatment approaches to central nervous system leukaemia.
Drugs. 1991 May;41(5):702-16. doi: 10.2165/00003495-199141050-00003.
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Cerebral abscesses produced by bacterial implantation and septic embolisation in primates.灵长类动物中由细菌植入和脓毒性栓塞引起的脑脓肿。
J Neurol Neurosurg Psychiatry. 1979 Jan;42(1):63-9. doi: 10.1136/jnnp.42.1.63.