Literature DB >> 1921926

Neurobehavioral toxicology of halothane in rats.

E D Levin1, E Uemura, R E Bowman.   

Abstract

Halothane, a commonly used general anesthetic, is considered to be relatively safe for that purpose. Chronic exposure, however, has been found to cause long-lasting damage to neural structure and impairment of behavioral function. In rats, behavioral alterations are particularly evident after developmental exposure, but they can also be seen with adult exposure, especially when halothane is given during the period of neural regrowth following a brain lesion. The pattern of neural damage includes retarded synaptogenesis, impaired dendritic branching and disruption of organelle structure. The behavioral syndrome includes learning impairment, decreased exploratory behavior and decreased nociceptive reactivity. In general, the neural pathology is more pronounced and more easily discernible than the behavioral effects. Neural damage, particularly to the hippocampus, can be clearly seen at points when behavioral impairments have not been found. This demonstrates that in some cases changes in neural structure can be more sensitive indicators of toxic damage than behavioral dysfunction. Halothane exposure has proved to be quite useful as an experimental tool in the study of neural and behavioral recovery after brain lesions. For example, after unilateral entorhinal cortical lesions, behavioral recovery and reactive synaptogenesis occur contemporaneously. It has not been demonstrated whether the behavioral recovery is due to this reinnervation. Postlesion halothane exposure almost completely suppresses reactive synaptogenesis, however, behavioral recovery of T-maze alternation behavior occurs in the halothane-treated rats as well as in controls. This suggests that recovery of spatial performance after such a lesion is not due to recovery of innervation in the dentate, but to some other process such as other neural systems taking over the functions lost with the brain lesion. The studies reviewed highlight the dangers of halothane exposure, especially during development or when recovering from brain injury. They also provide a good case study for comparing the relative sensitivity of morphological and behavioral measures in toxicology and point to the potential use of halothane as an experimental tool for examining the relationships between neural structure and behavioral function.

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Year:  1991        PMID: 1921926     DOI: 10.1016/0892-0362(91)90096-f

Source DB:  PubMed          Journal:  Neurotoxicol Teratol        ISSN: 0892-0362            Impact factor:   3.763


  16 in total

1.  Early Developmental Exposure to Repetitive Long Duration of Midazolam Sedation Causes Behavioral and Synaptic Alterations in a Rodent Model of Neurodevelopment.

Authors:  Jing Xu; Reilley Paige Mathena; Shreya Singh; Jieun Kim; Jane J Long; Qun Li; Sue Junn; Ebony Blaize; Cyrus David Mintz
Journal:  J Neurosurg Anesthesiol       Date:  2019-01       Impact factor: 3.956

Review 2.  Review: effects of anesthetics on brain circuit formation.

Authors:  Meredith Wagner; Yun Kyoung Ryu; Sarah C Smith; Piyush Patel; Cyrus D Mintz
Journal:  J Neurosurg Anesthesiol       Date:  2014-10       Impact factor: 3.956

3.  Learning about cognition risk with the radial-arm maze in the developmental neurotoxicology battery.

Authors:  Edward D Levin
Journal:  Neurotoxicol Teratol       Date:  2015-05-23       Impact factor: 3.763

Review 4.  Integrated defense system overlaps as a disease model: with examples for multiple chemical sensitivity.

Authors:  S C Rowat
Journal:  Environ Health Perspect       Date:  1998-02       Impact factor: 9.031

5.  Using animal models to evaluate the functional consequences of anesthesia during early neurodevelopment.

Authors:  Susan E Maloney; Catherine E Creeley; Richard E Hartman; Carla M Yuede; Charles F Zorumski; Vesna Jevtovic-Todorovic; Krikor Dikranian; Kevin K Noguchi; Nuri B Farber; David F Wozniak
Journal:  Neurobiol Learn Mem       Date:  2018-03-14       Impact factor: 2.877

Review 6.  Neurogenesis and developmental anesthetic neurotoxicity.

Authors:  Eunchai Kang; Daniel A Berg; Orion Furmanski; William M Jackson; Yun Kyoung Ryu; Christy D Gray; C David Mintz
Journal:  Neurotoxicol Teratol       Date:  2016-10-14       Impact factor: 3.763

7.  Long-lasting behavioral effects in neonatal mice with multiple exposures to ketamine-xylazine anesthesia.

Authors:  Lianyan Huang; Scott Hayes; Guang Yang
Journal:  Neurotoxicol Teratol       Date:  2016-09-10       Impact factor: 3.763

8.  Update on neonatal anesthetic neurotoxicity: insight into molecular mechanisms and relevance to humans.

Authors:  Piyush Patel; Lena Sun
Journal:  Anesthesiology       Date:  2009-04       Impact factor: 7.892

9.  Anesthetics interfere with the polarization of developing cortical neurons.

Authors:  Cyrus David Mintz; Sarah C Smith; Kendall M S Barrett; Deanna L Benson
Journal:  J Neurosurg Anesthesiol       Date:  2012-10       Impact factor: 3.956

10.  Isoflurane protects against human endothelial cell apoptosis by inducing sphingosine kinase-1 via ERK MAPK.

Authors:  Adnan M Bakar; Sang Won Park; Mihwa Kim; H Thomas Lee
Journal:  Int J Mol Sci       Date:  2012-01-17       Impact factor: 6.208

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