Literature DB >> 8301343

Sequential change of capillary permeability in the rat brain after surgical removal of an experimental brain tumor.

A Hodozuka1, K Sako, Y Yonemasu.   

Abstract

Experimental brain tumors were excised from rats for sequential observation of changes in local capillary permeability during the postsurgical period. Experimental brain tumor-bearing rats were prepared by stereotaxic transplantation of cultured tumor cells and the resultant tumor was delineated by administration of a dye. Following excision of the stained tumor by craniotomy, sequential changes in local capillary permeability were quantitatively followed-up by autoradiography, using 14C-amino-isobutyric acid as a tracer. Capillary permeability was enhanced following surgery, reaching a maximum both in the extent and degree on the third day. After undergoing a gradual reduction, it showed a marked increase for the second time in a very small area on the 10th postoperative day. A recurrence of the tumor was responsible for this late but marked increase. For a control group, the caudate nucleus was excised from normal rats, followed by observation of the sequential changes in the local capillary permeability. Due to surgical procedure, capillary permeability reached a maximum both in the extent and degree on the 5th postoperative day (slightly later than in the tumor group). This change in capillary permeability was less pronounced than in the tumor group. The difference in the conditions of surgery--tumor excision and partial excision of a normal brain tissue--appeared to explain this difference. The results of this study indicated that it is more desirable to give water-soluble antineoplastic agents early during the postoperative period for chemotherapy of a malignant brain tumor after surgery.

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Year:  1993        PMID: 8301343     DOI: 10.1007/BF01057033

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  24 in total

1.  The morphopathologic substrates of concussion?

Authors:  J T Povlishock; D P Becker; J D Miller; L W Jenkins; W D Dietrich
Journal:  Acta Neuropathol       Date:  1979-06-15       Impact factor: 17.088

2.  The uptake, distribution, and antitumor activity of 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea in the murine glioma.

Authors:  V A Levin; W R Shapiro; T P Clancy; V T Oliverio
Journal:  Cancer Res       Date:  1970-10       Impact factor: 12.701

Review 3.  A pharmacologic basis for brain tumor chemotherapy.

Authors:  V A Levin
Journal:  Semin Oncol       Date:  1975-03       Impact factor: 4.929

Review 4.  [Chemotherapy of malignant brain tumors: biology and pharmacokinetics (author's transl)].

Authors:  T Hoshino
Journal:  No Shinkei Geka       Date:  1980-11

5.  Permeability characteristics of brain adjacent to tumors in rats.

Authors:  V A Levin; M Freeman-Dove; H D Landahl
Journal:  Arch Neurol       Date:  1975-12

6.  Chemotherapy of an experimental glioma with nitrosoureas.

Authors:  C H Tator; A Day; R Ng; L Liberman
Journal:  Cancer Res       Date:  1977-02       Impact factor: 12.701

7.  Chloroethyl-cyclohexyl-nitrosourea (CCNU) in the treatment of malignant brain tumors.

Authors:  M L Rosenblum; A F Reynolds; K A Smith; B H Rumack; M D Walker
Journal:  J Neurosurg       Date:  1973-09       Impact factor: 5.115

8.  Regional blood flow and capillary permeability in the ethylnitrosourea-induced rat glioma.

Authors:  K Yamada; T Hayakawa; Y Ushio; N Arita; A Kato; H Mogami
Journal:  J Neurosurg       Date:  1981-12       Impact factor: 5.115

9.  Treatment of malignant glioma. A controlled study of chemotherapy and irradiation.

Authors:  W R Shapiro; D F Young
Journal:  Arch Neurol       Date:  1976-07

10.  A new approach to cancer chemotherapy: selective enhancement of tumor blood flow with angiotensin II.

Authors:  M Suzuki; K Hori; I Abe; S Saito; H Sato
Journal:  J Natl Cancer Inst       Date:  1981-09       Impact factor: 13.506

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