1. Effects of different doses of tenoxicam on spinal cord and meninges. Experimental study in dogs
- Author
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Ganem, Eliana Marisa [UNESP], Vianna, Pedro Thadeu Galvão [UNESP], Castiglia, Yara Marcondes Machado [UNESP], Braz, José Reinaldo Cerqueira [UNESP], Do Nascimento, P. [UNESP], Vanne, L. A. [UNESP], and Universidade Estadual Paulista (Unesp)
- Subjects
animal experiment ,etomidate ,anesthesia ,fentanyl ,regional, spinal block [Anesthetic techniques] ,animal tissue ,histology ,tenoxicam ,male ,nonsteroid antiinflammatory agent ,lumbar puncture ,dog [Animal] ,controlled study ,rat ,neurotransmission ,nonhuman ,tenoxican [Anti-inflammatory] ,animal model ,serotoninergic system ,spinal cord ,lumbar spinal cord ,n methyl dextro aspartic acid receptor ,prostaglandin synthesis inhibition ,sacral spinal cord ,female ,dog ,prostaglandin ,meninx ,intrathecal drug administration ,glycine - Abstract
Submitted by Vitor Silverio Rodrigues (vitorsrodrigues@reitoria.unesp.br) on 2014-05-27T11:19:42Z No. of bitstreams: 0Bitstream added on 2014-05-27T14:44:34Z : No. of bitstreams: 1 2-s2.0-0032892828.pdf: 46691 bytes, checksum: a53cdc2b60cfe48b103e86ad6998978c (MD5) Made available in DSpace on 2014-05-27T11:19:42Z (GMT). No. of bitstreams: 0 Previous issue date: 1999-01-27 Background and Objectives. The analgesic actions of nonsteroidal anti-inflammatory drugs (NSAID) result from the inhibition of the peripheral synthesis of prostaglandins. In spite of the emphasis on the peripheral action, several studies have shown the potential central action of such drugs. In rats, NSAID doses insufficient to block pain when systemically administered were effective when intrathecally injected. This effect could be mediated by interaction with descending serotoninergic ways together with neurotransmission modulation of glycine or N-methyl-D-aspartate receptors. Our goal was to study the effect of different tenoxican doses in the histology of dogs spinal cord and meninges. Methods. Thirty two dogs (7 to 17 kg) were randomly distributed in four groups: G1 - Control with distilled water (DW); G2 - 2 mg tenoxican diluted in DW; G3 - 4 mg tenoxican diluted in DW; G4 - 10 mg tenoxican diluted in DW in a constant volume of 1 ml. Anesthesia was induced with etomidate and fentanyl and dural puncture was performed with a 25G spinal needle in interspace L6-7. Animals were observed for 72 hours and subsequently euthanized by electrocution. Lumbar and sacral spinal cord segments were removed for further histologic examination. Results. All animals were clinically normal during the observation period and there has been no histologic alteration of the nervous system and meninges. Conclusions. In our experimental model intrathecal tenoxican doses up to 10 mg have not triggered nervous tissue or meningeal injuries in dogs. Departamento de Anestesiologia FMB-UNESP, Caixa Postal 530, 18618-000 Botucatu, SP Departamento de Anestesiologia FMB-UNESP, Caixa Postal 530, 18618-000 Botucatu, SP
- Published
- 1999