TY - JOUR
T1 - Neurotoxicity of intrathecally administered tetracaine commences at the posterior roots near entry into the spinal cord
AU - Takenami, Tamie
AU - Yagishita, Saburo
AU - Asato, Fumio
AU - Hoka, Sumio
N1 - Funding Information:
From the Department of Anesthesiology, Kitasato University (T.T., F.A., S.H.), Kanagawa, Japan; and the Department of Pathology, Kanagawa Rehabilitation Center (S.Y.), Kanagawa, Japan. Accepted for publication January 12, 2000. Supported by Health Science Research Grants for Comprehensive Research on Aging and Health (H10-Aging-008), Ministry of Health and Welfare, Japan. Presented in part at the Annual meeting of the American Society of Anesthesiologists, Orlando, FL, October 17-21, 1998. Reprint requests: Tamie Takenami, M.D., Department of Anesthesiology, Kitasato University School of Medicine, 1-15-1 Kita-sato, Sagamihara-shi, Kanagawa 228-8555, Japan. Painr Medicine.2000by the American Society of Regional Anesthesia and
PY - 2000/7
Y1 - 2000/7
N2 - Background and Objectives: Neurotoxicity of intrathecally administered local anesthetics is generating increased interest. This study was designed to examine the histopathologic effects of intrathecally administered tetracaine. Methods: Sixty Wistar rats randomly received either 20%, 10%, 5%, 3%, 1%, 0.5%, or 0% tetracaine dissolved in 10% glucose solution or no solution via a chronically implanted intrathecal catheter. The spinal cord at L1, posterior and anterior roots and cauda equina were excised 5 days later, sectioned, processed, and prepared for light and electron microscopic examinations. Results: Rats treated with tetracaine at 10% or 20% developed lesions in the posterior white matter and posterior roots. Rats injected with 3% or 5% tetracaine developed lesions, which began in the posterior roots close to the spinal cord and extended to the posterior white matter. The lesions were characterized by axonal degeneration. Injections of ≤ 1% of tetracaine did not cause any pathological changes. Conclusions: Our results suggest that the initial target of intrathecal tetracaine neurotoxicity may be the posterior roots at their entry into the spinal cord, where the axons are devoid of myelin sheath and thus representing a sensitive area for neurotoxic change.
AB - Background and Objectives: Neurotoxicity of intrathecally administered local anesthetics is generating increased interest. This study was designed to examine the histopathologic effects of intrathecally administered tetracaine. Methods: Sixty Wistar rats randomly received either 20%, 10%, 5%, 3%, 1%, 0.5%, or 0% tetracaine dissolved in 10% glucose solution or no solution via a chronically implanted intrathecal catheter. The spinal cord at L1, posterior and anterior roots and cauda equina were excised 5 days later, sectioned, processed, and prepared for light and electron microscopic examinations. Results: Rats treated with tetracaine at 10% or 20% developed lesions in the posterior white matter and posterior roots. Rats injected with 3% or 5% tetracaine developed lesions, which began in the posterior roots close to the spinal cord and extended to the posterior white matter. The lesions were characterized by axonal degeneration. Injections of ≤ 1% of tetracaine did not cause any pathological changes. Conclusions: Our results suggest that the initial target of intrathecal tetracaine neurotoxicity may be the posterior roots at their entry into the spinal cord, where the axons are devoid of myelin sheath and thus representing a sensitive area for neurotoxic change.
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U2 - 10.1053/rapm.2000.6444
DO - 10.1053/rapm.2000.6444
M3 - Article
C2 - 10925933
AN - SCOPUS:0034235098
SN - 1098-7339
VL - 25
SP - 372
EP - 379
JO - Regional Anesthesia and Pain Medicine
JF - Regional Anesthesia and Pain Medicine
IS - 4
ER -