Fadic_1989_J.Neurosci.Res_22_449

Reference

Title : Nerve regulation of class I and class II-asymmetric forms of acetylcholinesterase in rat skeletal muscles - Fadic_1989_J.Neurosci.Res_22_449
Author(s) : Fadic R , Inestrosa NC
Ref : Journal of Neuroscience Research , 22 :449 , 1989
Abstract :

Two classes of collagen-tailed, asymmetric forms (A-forms) of acetylcholinesterase (AChE) have been described in skeletal muscles of vertebrates. They are distinguished by their different solubilization requirements: class I A-forms are solubilized in the presence of high salt, whereas class II A-forms require in addition a chelating agent for solubilization. We report here that class II A-forms are less sensitive to nerve section than are class I A-forms. The latter form decreases faster and to a lower level of activity after denervation. The decay of both AChE classes is more rapidly in short-stump nerves than in long ones. The effect of nerve section on class II A-forms appears to be dependent on the particular muscle group being studied. Both classes of A-forms reappear after muscle reinnervation, but the class I A-forms recovered earlier. More interestingly, both classes of A-forms increase in normally innervated skeletal muscles after contralateral nerve injury. In this case, however, the class II A-forms change first. Muscular disuse induced by contralateral tenotomy is also followed by a rise in class II A-forms. Our results, showing differences in response and flexibility in the changes of the two classes of A-forms in several experimental conditions, represent a relevant contribution to the understanding of the regulation and functional role of the asymmetric forms of AChE in vertebrate skeletal muscles.

PubMedSearch : Fadic_1989_J.Neurosci.Res_22_449
PubMedID: 2760943

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Citations formats

Fadic R, Inestrosa NC (1989)
Nerve regulation of class I and class II-asymmetric forms of acetylcholinesterase in rat skeletal muscles
Journal of Neuroscience Research 22 :449

Fadic R, Inestrosa NC (1989)
Journal of Neuroscience Research 22 :449