Data di Pubblicazione:
2008
Abstract:
Neurodegenerative processes are one of the main age-related features of dogs. Senile neurodegeneration
can be clinically asymptomatic, ‘‘borderline’’ (i.e., a condition that is intermediate between
normal and disease state) or progress toward overt clinical abnormalities, known as age-related cognitive
disorders, cognitive dysfunction syndrome (CDS), or senile dementia. The aim of the present article is to
review the rationale for the use of phosphatidylserine (PS), a natural phospholipid, in the management of
brain neurodegenerative processes in senior dogs. The preliminary clinical data on PS supplementation
in senior dogs will also be reviewed. There is evidence that PS is absorbed rapidly, reaches high concentrations
in the brain, and is well tolerated. Phosphatidylserine has emerged to exert several in vitro and in
vivo neuroprotective activities. It has been shown to positively affect neurotransmitter release and neurotransmitter
receptor density in several brain regions from laboratory animals with memory impairments.
Phosphatidylserine also was found to revert experimentally-induced amnesia in rats and
improve memory deficits both in old animals and in elderly humans with various degrees of cognitive
impairment and Alzheimer’s dementia. On the basis of the data reported in the scientific literature, PS
stands out as an essential ‘‘brain nutrient.’’ In view of these features, some supplements containing PS
have been licensed recently as adjuvant treatment for canine and feline brain aging. The results of the
studies on its use in the preventative and combined treatment of dogs with clinical features consistent
with the diagnosis of CDS are reported. Although PS-based neuroprotection in dogs and cats is still at
its infancy, the preliminary collected data look promising and thus merit further investigation.
Tipologia CRIS:
03A-Articolo su Rivista
Keywords:
Phosphatidylserine; aging; nutraceutic; dog; brain
Elenco autori:
Osella M.C.; Re G.; Badino P.; Bergamasco L.; Miolo A.
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