1 April 2002, vol. 8, no. 2, pp. 130-138(9)
Moscarello MA; Mak B; Nguyen TA; Wood DD; Mastronardi F; Ludwin SK
 Departments of Structural Biology and Biochemistry, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, Canada M5G 1X8
 Department of Surgery, University of Washington, Seattle, Washington, USA
 Departments of Structural Biology and Biochemistry, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, M5G 1X8; 2Department
 Department of Pathology, Queen's University and Kingston General Hospital, Kingston, Ontario, Canada
Treatment with paclitaxel by four intraperitoneal injections (20 mg/kg) 1 week apart attenuated clinical signs in a spontaneously demyelinating model, if given with onset of clinical signs.
If given at 2 months of age (1 month prior to clinical signs), disease was almost completely prevented.
The astrogliosis, prominent in our model, was reversed by paclitaxel as determined by astrocyte counts and quantitation of GFAP.
Electron microscopic examination of affected regions at 2.5 months demonstrated that the myelin was generally normal.
By 4 months of age, demyelination was common in the superior cerebellar peduncle, maximal at 6 months, but continued to 8 months.
In addition to myelin vacuolation and nude axons, the presence of many thin myelin sheaths suggested remyelination or partial demyelination.
Although no evidence of oligodendrocyte loss was seen, nuclear changes were observed.
To substantiate that remyelination was occurring, we measured MBP (18.5 kDa), MBP-exon II, Golli-MBP, TP8, Golli-MBP-J37, platelet-derived growth factor a (PDGFR a) and sonic hedgehog (SHH).
Of these TP8, PDGFR a and SHH were up-regulated in the untreated transgenic.
After paclitaxel treatment, MBP-Exon II, TP8, PDGFR a and SHH were further up-regulated.
We concluded that some of the effects of paclitaxel were to stimulate
proteins involved in early myelinating events possibly via a signal transduction
© 2002 ingenta