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Home > Journals > Journal of Neurosurgical Sciences > Past Issues > Journal of Neurosurgical Sciences 2003 September;47(3) > Journal of Neurosurgical Sciences 2003 September;47(3):149-55

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CURRENT ISSUEJOURNAL OF NEUROSURGICAL SCIENCES

A Journal on Neurosurgery

Indexed/Abstracted in: e-psyche, EMBASE, PubMed/MEDLINE, Neuroscience Citation Index, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 1,651

Frequency: Bi-Monthly

ISSN 0390-5616

Online ISSN 1827-1855

 

Journal of Neurosurgical Sciences 2003 September;47(3):149-55

    ORIGINAL ARTICLES

Effects of Ginko Biloba and caspase inhibitors on brain ischemia in the Mongolian Gerbil

Donato G. 1, Volpentesta G. 2, Lavano A. 2, Ferraro G. 2, Signorelli F. 3, Amorosi A. 1, Maltese L. 1, De Sarro G. B. 4, Signorelli C. D. 2

1 Section of Pathology Department of Experimental and Clinical Medicine “G. Salvatore”, Faculty of Medicine “Magna Graecia” University, Catanzaro, Italy
2 Section of Neurosurgery Department of Experimental and Clinical Medicine “G. Salvatore”, Faculty of Medicine “Magna Graecia” University, Catanzaro, Italy
3 CHU Pierre Werthemaire, Lyon, France
4 Section of Pharmacology Department of Experimental and Clinical Medicine “G. Salvatore”, Faculty of Medicine “Magna Graecia” University, Catanzaro, Italy

Aim. Data reported in previous studies and our own previous experience have led us to explore the mechanism of and the degree of protection afforded by Ginko Biloba in a model of cerebral ischemia in the Mongolian Gerbil evaluating histological and neurological effects in this rodent.
Methods. Mongolian Gerbils were divided into experimental groups: Group A consisted of animals subjected only to experimental ischemia; 5 minutes occlusion of the carotid arteries. Group B consisted of animals subjected to experimental ischemia and to a dose of Ginko Biloba, given intraperitoneally immediately before the surgical procedure. Group C consisted of animals subjected to experimental ischemia and to a dose of Ginko Biloba, given intraperitoneally immediately after the surgical procedure. Group D consisted of animals subjected to experimental ischemia and to a dose of the caspase inhibitors z-VAD.FMK and z-DEVD.FMK injected intracerebroventricularly through the right hemisphere before the surgical procedure. Group E consisted of animals subjected to experimental ischemia and to a dose of caspase inhibitors injected after the surgical procedure. Group F consisted of Sham-operated animals. Histological controls were done by H and E and the TUNEL method in the frontal cortex and caudate-putamen.
Results. The percentage of normal cells was not statistically significant at analysis with H and E, whereas the TUNEL method showed good protection with Ginko Biloba and caspase inhibitors, when the latter is given in the reperfusion phase. These data were in agreement with data obtained at neurological examination.
Conclusion. We could say that cellular morphology is in itself an untrustworthy tool for judging the effects of ischemia and protective drugs; the TUNEL method may add important information about the different components of cellular death; the reperfusion phase may be critical for apoptotic phenomena; Ginko Biloba might protect neurons of the frontal cortex from both necrotic and apoptotic death in this model of ischemia.

language: English


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