“…In vivo MRS provides a means to study the compounds involved in phospholipid metabolism. Altered phospholipid metabolism has been suggested in bipolar disorder (Deicken et al 1995), schizophrenia (Pettegrew et al 1991;Stanley et al 1994Stanley et al , 1995, substance abuse Kaufman et al 1996), Alzheimer's disease (Pettegrew et al 1988;Nitsch et al 1992;Smith et al 1993;Klunk et al 1996), and normal aging (Pettegrew et al 1990). A treatment that could reverse or prevent changes in phospholipid metabolism seen in these circumstances would be valuable.…”
The increases in phosphodiesters seen in this study indicate that phospholipid synthesis and turnover were stimulated by 6 weeks of oral citicoline. These results in humans support previous in vitro and animal studies and suggest that the administration of oral citicoline may be of use in reversing age-related changes in the brain.
“…In vivo MRS provides a means to study the compounds involved in phospholipid metabolism. Altered phospholipid metabolism has been suggested in bipolar disorder (Deicken et al 1995), schizophrenia (Pettegrew et al 1991;Stanley et al 1994Stanley et al , 1995, substance abuse Kaufman et al 1996), Alzheimer's disease (Pettegrew et al 1988;Nitsch et al 1992;Smith et al 1993;Klunk et al 1996), and normal aging (Pettegrew et al 1990). A treatment that could reverse or prevent changes in phospholipid metabolism seen in these circumstances would be valuable.…”
The increases in phosphodiesters seen in this study indicate that phospholipid synthesis and turnover were stimulated by 6 weeks of oral citicoline. These results in humans support previous in vitro and animal studies and suggest that the administration of oral citicoline may be of use in reversing age-related changes in the brain.
“…The findings in early AD are in accordance with in vitro studies suggesting that reduced PLA 2 activity may contribute to Aβ production (Emmerling et al 1993(Emmerling et al , 1996Nitsch et al 1997;Cho et al 2006); the findings in late AD are in line with the studies of Stephenson et al (1996Stephenson et al ( , 1999 and Moses et al (2006), showing a correlation between increased PLA 2 immunoreactivity and Aβ-containing plaques. Finally, in autopsy specimens of parietal lobe gray matter from subjects with severe AD, greater PDE was correlated with the density of neurofibrillary tangles (Smith et al 1993). Data described in this subtitle are summarized in Table 2.…”
Section: Reduced Brain Pla 2 Activity In Early-stage Alzheimer Diseasementioning
The use of positive modulators of PLA2 (especially of cPLA2 and iPLA2) or supplementation with dietary lipid compounds (e.g., arachidonic acid) in combination with cognitive training could be a valuable therapeutic strategy for cognitive enhancement in early-stage AD.
“…The findings in early AD are in accordance with in vitro studies suggesting that reduced PLA 2 activity may contribute to Aβ production (Emmerling et al 1993(Emmerling et al , 1996Nitsch et al 1997;Cho et al 2006); the findings in late AD are in line with the studies of Stephenson et al (1996Stephenson et al ( , 1999 and Moses et al (2006) showing a correlation between increased PLA 2 immunoreactivity and Aβ-containing plaques. Finally, in autopsy specimens of parietal lobe gray matter from subjects with severe AD, greater PDE was correlated with the density of neurofibrillary tangles (Smith et al 1993).…”
Section: Alterations Of Phospholipase a 2 And Phospholipid Metabolismmentioning
Activation and inhibition of specific PLA(2) isoforms at different stages of AD could be of therapeutic importance and delay cognitive dysfunction and neurodegeneration.
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