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Cholesterol Synthesis and Nerve Regeneration
Author(s) -
Heacock Anne M.,
Klinger Paul D.,
Seguin Edward B.,
Agranoff Bernard W.
Publication year - 1984
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.1984.tb12701.x
Subject(s) - desmosterol , optic nerve , cholesterol , axoplasmic transport , neurite , tectum , retinal , regeneration (biology) , retina , biochemistry , biology , in vivo , in vitro , chemistry , central nervous system , endocrinology , microbiology and biotechnology , anatomy , sterol , midbrain , neuroscience
In this report, we examine the requirement of cholesterol biosynthesis and its axonal transport for goldfish optic nerve regeneration. Cholesterol, labeled by intraocular injection of [ 3 H]mevalonolactone. exhibited a delayed appearance in the optic tectum. Squalene and other minor components were labeled but not transported. Following optic nerve crush, the amount of labeled cholesterol transport was elevated, while retinal labeling was not altered relative to control fish. A requirement for cholesterol biosynthesis is inferred from the inhibition of neurite outgrowth in retinal explants caused by the cholesterol synthesis inhibitor, 20, 25‐diazacholes‐terol. The inhibition of growth could be overcome by addition of mevalonolactone, but not cholesterol, to the medium. Intraperitoneal administration of 200 nmol of dia‐zacholesterol resulted in 92‐98% inhibition of retinal cholesterol synthesis and accumulation of labeled des‐mosterol and other lipids in fish retina and brain which persisted for 2 weeks. Diazacholesterol‐treated fish showed no reduction in the amount of lipid‐soluble radioactivity transported following intraocular injection of [ 3 H]mevalonolactone, but there were alterations in the chromatographic pattern of the transported labeled lipids. In contrast to its effects on neurite outgrowth in vitro , diazacholesterol did not inhibit optic nerve regeneration in vivo , as measured both by arrival of labeled rapidly transported protein at the tectum and by time required for the return of visual function.