The tissue level of dexamethasone in human brain tumors is about 1000 times lower than the cytotoxic concentration in cell culture

被引:12
作者
Nestler, U [1 ]
Winking, M [1 ]
Böker, DK [1 ]
机构
[1] Univ Giessen, Dept Neurosurg, D-35385 Giessen, Germany
关键词
dexamethasone; tissue level; cell culture; cytotoxicity; brain tumor; glioblastoma;
D O I
10.1179/016164102101200203
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In glioblastoma patients dexamethasone is routinely administered as an antiedematous drug. In contrast to its empirically proven effect, the biochemical way of action remains poorly understood. In order to assess whether a direct cytotoxic effect is present in vivo we compared dexamethasone levels in brain tumor specimens with its cytotoxic concentrations in cell culture. Biopsy specimens were taken during microsurgical tumor removal, homogenized and dexamethasone levels were measured by high pressure liquid chromatography, In cell culture we tested different concentrations of dexamethasone on A172, U87, U373 cells and on eleven primary glioblastoma cell lines. Furthermore a pilocytic astrocytoma I, an astrocytoma It and an oligodendroglioma III and a meningioma were examined. Cell viability was assessed using the Alamar Blue assay and the concentrations resulting in loss of 50% of the cell population were calculated (LD50), The average brain tumor tissue concentration of dexamethasone was 225 nanogram g(-1). The mean LD50 in cell culture ranged at 222 microgram ml(-1). We conclude that a direct cytotoxic effect of dexamethasone on brain tumor cells is not present in vivo because the tissue levels of the drug are about 1000 times lower than the LD50 in cell culture.
引用
收藏
页码:479 / 482
页数:4
相关论文
共 15 条
  • [1] BERNDT SF, 1973, JOINT M BRIT GERM PH
  • [2] FACTORS RESPONSIBLE FOR THE RETENTION OF FLUID IN HUMAN-TUMOR EDEMA AND THE EFFECT OF DEXAMETHASONE
    BODSCH, W
    ROMMEL, T
    OPHOFF, BG
    MENZEL, J
    [J]. JOURNAL OF NEUROSURGERY, 1987, 67 (02) : 250 - 257
  • [3] DREWS J, 1986, IMMUNOPHARMAKOLOGIE
  • [4] NEOPLASTIC AND PHARMACOLOGICAL INFLUENCE ON THE PERMEABILITY OF AN IN-VITRO BLOOD-BRAIN-BARRIER
    GRABB, PA
    GILBERT, MR
    [J]. JOURNAL OF NEUROSURGERY, 1995, 82 (06) : 1053 - 1058
  • [5] Mechanism of dexamethasone suppression of brain tumor-associated vascular permeability in rats - Involvement of the glucocorticoid receptor and vascular permeability factor
    Heiss, JD
    Papavassiliou, E
    Merrill, MJ
    Nieman, L
    Knightly, JJ
    Walbridge, S
    Edwards, NA
    Oldfield, EH
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (06) : 1400 - 1408
  • [6] IMPLICATION OF GLUCOCORTICOID RECEPTORS IN THE STIMULATION OF HUMAN GLIOMA CELL-PROLIFERATION BY DEXAMETHASONE
    LANGEVELD, CH
    VANWAAS, MP
    STOOF, JC
    SUTANTO, W
    DEKLOET, ER
    WOLBERS, JG
    HEIMANS, JJ
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 1992, 31 (03) : 524 - 531
  • [7] MACUNIAS RJ, 1993, NEUROSURGERY, V33, P485
  • [8] EFFECTS OF DEXAMETHASONE AND METHYLPREDNISOLONE ON CELL CULTURES OF HUMAN GLIOBLASTOMAS
    MEALEY, J
    CHEN, TT
    SCHANZ, GP
    [J]. JOURNAL OF NEUROSURGERY, 1971, 34 (03) : 324 - &
  • [9] Dexamethasone-mediated protection from drug cytotoxicity: association with p21WAF1/CIP1 protein accumulation?
    Naumann, U
    Durka, S
    Weller, M
    [J]. ONCOGENE, 1998, 17 (12) : 1567 - 1575
  • [10] PAGE B, 1993, INT J ONCOL, V3, P473