Lipids of nervous tissue: Composition and metabolism

Ps, Sastry

doi:10.1016/0163-7827(85)90011-6

Cited by 688 publications

(438 citation statements)

References 1,199 publications

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“…7 Both of these fatty acids are present at low concentrations in brain. 7,8 Epidemiological observations point to a decreased dietary n-3 polyunsaturated fatty acid (PUFA) intake being associated with an increased prevalence of bipolar disorder. 9 Blood DHA levels 10,11 and postmortem prefrontal cortex DHA levels are 16.5% lower in bipolar patients compared to normal controls.…”

Section: Introductionmentioning

confidence: 99%

n-3 Polyunsaturated fatty acid deprivation in rats decreases frontal cortex BDNF via a p38 MAPK-dependent mechanism

et al. 2006

Mol Psychiatry

258

151

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Decreased docosahexaenoic acid (DHA) and brain-derived neurotrophic factor (BDNF) have been implicated in bipolar disorder. It also has been reported that dietary deprivation of n-3 polyunsaturated fatty acids (PUFAs) for 15 weeks in rats, increased their depression and aggression scores. Here, we show that n-3 PUFA deprivation for 15 weeks decreased the frontal cortex DHA level and reduced frontal cortex BDNF expression, cAMP response element binding protein (CREB) transcription factor activity and p38 mitogen-activated protein kinase (MAPK) activity. Activities of other CREB activating protein kinases were not significantly changed. The addition of DHA to rat primary cortical astrocytes in vitro, induced BDNF protein expression and this was blocked by a p38 MAPK inhibitor. DHA's ability to regulate BDNF via a p38 MAPK-dependent mechanism may contribute to its therapeutic efficacy in brain diseases having disordered cell survival and neuroplasticity.

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Section: Introductionmentioning

confidence: 99%

n-3 Polyunsaturated fatty acid deprivation in rats decreases frontal cortex BDNF via a p38 MAPK-dependent mechanism

et al. 2006

Mol Psychiatry

258

151

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“…Under physiologic conditions both lecithin and sphingomyelin are subject to continuous breakdown and resynthesis. Although glycerophospholipids are more stable in myelin than in other membranes with turnover rates between 1 week and 1 month (39), such rates also depend on the lipid side-chain composition which in turn exhibits regional variations (37,38). Because PCh and GPC are part of the metabolic pathway of lecithin and sphingomyelin, the concentration of Cho and the content of the choline-containing phospholipids in a certain brain region will be roughly correlated.…”

Section: Choline-containing Compoundsmentioning

confidence: 99%

“…These compounds are involved in the metabolism of the membrane lipids phosphatidylcholine (i.e., lecithin) and ceramidephosphocholine (i.e., sphingomyelin) (37,38). Due to its high myelin content, white matter contains more lipids than gray matter (15.6% versus 5.9% of total wet weight) and also shows a different lipid composition.…”

Section: Choline-containing Compoundsmentioning

confidence: 99%

Regional metabolite concentrations in human brain as determined by quantitative localized proton MRS

Pouwels

Frahm

1998

Magnetic Resonance in Med

428

322

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The regional distribution of brain metabolites was studied in several cortical white and gray matter areas, cerebellum, and thalamus of young adults with use of quantitative single-voxel proton MRS at 2.0 T. Whereas the neuronal compound Nacetylaspartate is distributed homogeneously throughout the brain, N-acetylaspartylglutamate increases caudally and exhibits higher concentrations in white matter than in gray matter. Creatine, myo-inositol, glutamate, and glutamine are less concentrated in cortical white matter than in gray matter. The highest creatine levels are found in cerebellum, parallel to the distribution of creatine kinase and energy-requiring processes in the brain. Also myo-inositol has highest concentrations in the cerebellum. Choline-containing compounds exhibit a marked regional variability with again highest concentrations in cerebellum and lowest levels and a strong caudally decreasing gradient in gray matter. The present findings neither support a metabolic gender difference (except for a 1.3-fold higher myo-inositol level in parietal white matter of female subjects) nor a metabolic hemispheric asymmetry.

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“…The function of membranes is to allow cellular compartmentalization, and impart an identity to individual cells and organelles, besides providing an appropriate environment for proper functioning of membrane proteins. Interestingly, cellular membranes in the nervous system are characterized by very high concentration and remarkable diversity of lipids, and these are correlated with increased complexity in the function of the nervous system (Sastry, 1985;Wenk, 2005). In this context, cholesterol represents an important lipid since brain cholesterol has been implicated in a number of neurological disorders (Chattopadhyay and Paila, 2007;Martín et al, 2014), some of which share a common etiology of defective cholesterol 4 metabolism in the brain (Porter and Herman, 2011).…”

mentioning

confidence: 99%

Molecular rheology of neuronal membranes explored using a molecular rotor: Implications for receptor function

Pal

Chakraborty

Bandari

et al. 2016

Chemistry and Physics of Lipids

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The role of membrane cholesterol as a crucial regulator in the structure and function of membrane proteins and receptors is well documented. However, there is a lack of consensus on the mechanism for such regulation. We have previously shown that the function of an important neuronal receptor, the serotonin1A receptor, is modulated by cholesterol in hippocampal membranes. With an overall objective of addressing the role of 3 membrane physical properties in receptor function, we measured the viscosity of hippocampal membranes of varying cholesterol content using a meso-substituted fluorophore (BODIPY-C12) based on the BODIPY probe. BODIPY-C12 acts as a fluorescent molecular rotor and allows measurement of hippocampal membrane viscosity through its characteristic viscosity-sensitive fluorescence depolarization. A striking feature of our results is that specific agonist binding by the serotonin1A receptor exhibits close correlation with hippocampal membrane viscosity, implying the importance of global membrane properties in receptor function. We envision that our results are important in understanding GPCR regulation by the membrane environment, and is relevant in the context of diseases in which GPCR signaling plays a major role and are characterized by altered membrane fluidity.Abbreviations: 2-AS, 2-(9-anthroyloxy)stearic acid; 12-AS, 12-(9-anthroyloxy)stearic acid; BODIPY, 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene; GPCR, G protein-coupled receptor; 8-12-PC, 1-palmitoyl-2-(12-doxyl)stearoyl-sn-glycero-3-phosphocholine; DMPC, 1,2-dimyristoyl-sn-glycero-3-phosphocholine; DOPC, 1,2-dioleoylsn-glycero-3-phosphocholine; MβCD, methyl-β-cyclodextrin; Tempo-PC, 1,2-dioleoyl-snglycero-3-phosphotempocholine Keywords: Molecular rotor; hippocampal membrane; viscosity; cholesterol; neuronal receptor IntroductionBiological membranes are complex, highly organized, two-dimensional, supramolecular assemblies of a diverse variety of lipids and proteins. The function of membranes is to allow cellular compartmentalization, and impart an identity to individual cells and organelles, besides providing an appropriate environment for proper functioning of membrane proteins. Interestingly, cellular membranes in the nervous system are characterized by very high concentration and remarkable diversity of lipids, and these are correlated with increased complexity in the function of the nervous system (Sastry, 1985;Wenk, 2005). In this context, cholesterol represents an important lipid since brain cholesterol has been implicated in a number of neurological disorders (Chattopadhyay and Paila, 2007;Martín et al., 2014), some of which share a common etiology of defective cholesterol 4 metabolism in the brain (Porter and Herman, 2011). More importantly, the function of neuronal receptors depends on cholesterol (Pucadyil and Chattopadhyay, 2006;Allen et al., 2007;Paila and Chattopadhyay, 2010;Jafurulla and Chattopadhyay, 2013), which affects neurotransmission, resulting in mood and anxiety disorders (Papakostas et al., 2004). In spite of ...

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Lipids of nervous tissue: Composition and metabolism

Cited by 688 publications

References 1,199 publications

n-3 Polyunsaturated fatty acid deprivation in rats decreases frontal cortex BDNF via a p38 MAPK-dependent mechanism

n-3 Polyunsaturated fatty acid deprivation in rats decreases frontal cortex BDNF via a p38 MAPK-dependent mechanism

Regional metabolite concentrations in human brain as determined by quantitative localized proton MRS

Molecular rheology of neuronal membranes explored using a molecular rotor: Implications for receptor function

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