• Reg Anesth Pain Med · Sep 2004

    Comparative Study

    Intrathecal mepivacaine and prilocaine are less neurotoxic than lidocaine in a rat intrathecal model.

    • Tamie Takenami, Saburo Yagishita, Yoshihiro Nara, and Sumio Hoka.
    • Department of Anesthesiology, Kitasato University School of Medicine, Kanagawa, Japan. takenami@med.kitasato-u.ac.jp
    • Reg Anesth Pain Med. 2004 Sep 1; 29 (5): 446-53.

    Background And ObjectivesHistologic evidence of the comparative neurotoxicity of lidocaine, mepivacaine, and prilocaine is incomplete. We compared the intrathecal neurotoxicity in rats among these 3 drugs based on morphologic and neurofunctional findings.MethodsRats (n=169) randomly received 0.12 microL/g of 0%, 2%, 5%, 7.5%, 10%, or 20% lidocaine, mepivacaine, or prilocaine or 25% glucose dissolved in distilled water via a chronically implanted intrathecal catheter. The effect of the agents on neurofunction was evaluated by movement of the hind limb (behavior test) and by sensory threshold (paw-stimulation test). The L1 spinal cord, the posterior and anterior roots, and the cauda equina were removed en bloc 5 days later and examined by light and electron microscopy.ResultsA significant decrease in sensory threshold or irreversible hind-limb limitation was observed only in rats receiving 20% lidocaine. Morphologic abnormalities characterized by axonal degeneration were observed in rats receiving > or =7.5% lidocaine, 20% mepivacaine, and 20% prilocaine, at the posterior white matter and the proximal portion of the posterior root just at the entrance into the spinal cord. The incidence of lesions was significantly higher in rats receiving lidocaine than mepivacaine and prilocaine.ConclusionIt is suggested that intrathecal mepivacaine and prilocaine are less neurotoxic than highly concentrated lidocaine in a rat intrathecal model.

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