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Volume 5, Issue 5 (Suppl)
J Neurol Disord, an open access journal
ISSN: 2329-6895
CNS 2017
October 02-03, 2017
Page 31
conference
series
.com
3
rd
International Conference on
Central Nervous System Disorders and Therapeutics
October 02-03, 2017 Vienna, Austria
Alessandro M Morelli, J Neurol Disord 2017, 5:5(Suppl)
DOI: 10.4172/2329-6895-C1-022
Metabolism of myelin in health and pathology
M
yelin is a site of active aerobic energy metabolism, producing ATP through the oxidative phosphorylation (OXPHOS)
machinery, which contributes to the acceleration of nervous impulse. This innovative view simplifies current ideas about
the physical chemical mechanisms that ensures the advancement of the action potential (CAP) as such basic mechanisms are
unchanged in the passage of the CAP from the non-myelinated to myelinated axon. The ATP produced in myelin sheath is
transferred to the axon through the Gap Junctions, which are abundant in myelin sheath. The OXPHOS proteins expresses in
myelin is closely related to that of mitochondria and hence there must be some process still to be defined, which guarantees
the transfer of OXPHOS machinery from mitochondria to myelin; overall the mitochondria-myelin link is known since many
mitochondrial pathologies primarily affect myelin. For perfect functioning, OXPHOS requires an active synthesis of the heme
group, considering that it is a fundamental component of several subunits of respiratory complexes, and interestingly, myelin
sheath displays a higher heme group synthesis in comparison with other districts. In particular, proper functioning of myelin
is closely linked to an efficient biosynthetic pathway of the heme and the crucial passage is catalyzed by the enzyme ALA
dehydratase (EC 4.2.1.24) that requires zinc as cofactor. Lead poisoning (Saturnism) results in an imbalance of this enzyme and
myelin degeneration. Moreover, analyzing the OXPHOS metabolism in myelin isolated from autopsy specimens of multiple
sclerosis (MS) patients, we have observed a defective energy/respiratory capacity. With this knowledge, the hypothesis that MS
is not an autoimmune disease, but a disease triggered by myelin degeneration following a malfunction of some process related
to its energy function and heavy metal pollution seems confirmed, also considering the historical link between industrialization
and the MS onset.
Biography
Alessandro M Morelli carried out research in varied fields of biology, focusing in those areas most directly linked to medicine. He investigated on the enzyme Glu-
cose-6-P-dehydrogenase and on its molecular mechanism of senescence. He has been working in the phototransduction molecular events in photoreceptor cells of
vertebrate retina. He has discovered the protein FX, a NADP dependent enzyme, catalyzing synthesis of GDP-L-fucose. He has been working on the effects of electro-
magnetic fields of extremely low frequency on the activity of enzymes involved in phototransduction in retinal cells of vertebrates. Moreover, he has put in evidence the
reversible effects of electromagnetic fields on lipid-linked enzymes such as acetylcholinesterase of retinal synaptosomes. Recently, with Isabella Panfoli, Silvia Ravera,
Daniela Calzia, he has discovered the brain myelin energetic function and the ATP extramitochondrial synthesis operating in it, involving new paradigms for neurobiology,
with application in the study of multiple sclerosis and other neurodegenerative diseases.
morellia@unige.itAlessandro MMorelli
University of Genoa, Italy