phosphatidylserine

What is phosphatidylserine

Phosphatidylserine (1, 2-diacyl-sn-glycero-3-phospho-L-serine) is the major anionic phospholipid in mammalian cell membranes and phosphatidylserine accounts for 13–15 % of the phospholipids in the human cerebral cortex 1). The brain is enriched in the two aminophospholipids, phosphatidylethanolamine and phosphatidylserine compared with other tissues. In the brain, and particularly in the retina 2), the acyl chains of phosphatidylserine are highly enriched in docosahexaenoic acid (DHA) 3). In human gray matter, docosahexaenoic acid (DHA) accounts for >36% of the fatty acyl species of phosphatidylserine 4). Phosphatidylserine has been shown to play a key role in the functioning of neuron membranes, such as signal transduction, secretory vesicle release and cell-to-cell communication 5). With aging, neural membrane fluidity is compromised due to the increased presence of cholesterol, a low incorporation rate and decreased levels of total polyunsaturated fatty acids, blockages to phospholipid pathways, and increases in free radicals, resulting in oxidative stress 6). At least 25 clinical trials suggested that consumption of phosphatidylserine supplement may reduce the risk of dementia and cognitive dysfunction in the elderly 7), 8). The administration of phosphatidylserine extracted from bovine cortex (bovine cortex-phosphatidylserine) has positive effects on brain function. Bovine cortex-phosphatidylserine was shown to improve learning and memory in age-associated memory impaired subjects 9), to enhance behavioral and cognitive parameters in geriatric patients 10), and to improve cognitive performance of Alzheimer’s disease patients 11). However, improvements lasted only a few months and were seen in people with the least severe symptoms. Initially, phosphatidylserine supplements were derived from the brain cells of cows (bovine cortex-phosphatidylserine). The bovine brain cortex phosphatidylserine was found to be enriched with docosahexaenoic acid (DHA) 12). But because of concerns about mad cow disease, most manufacturers now produce the supplements from soy lecithin, sunflower lecithin or cabbage derivatives. However, soybean-derived phosphatidylserine does not contain docosahexaenoic acid (DHA), and clinical studies have demonstrated inconclusive efficacy results 13). Preliminary studies have shown that plant-based phosphatidylserine supplements may also offer benefits, but more research is needed. However, no modern studies have continued to focus on phosphatidylserine, suggesting its limited effect.

Phosphatidylserine supplement has been approved by the U.S. Food and Drug Administration 14) to treat memory deficit disorders such as Alzheimer’s disease and other forms of dementia, to support healthy cognitive function during aging, and to remediate cognitive deficits as a result of heavy drinking and cigarette smoking. The mechanism by which phosphatidylserine- omega-3 (DHA) exerts its effects is not fully understood, however phosphatidylserine has been found to regulate key proteins in neuronal membranes, including sodium/calcium ATPase 15), protein kinase C 16) and Raf-1 protein kinase 17). Phosphatidylserine was also found to influence neurotransmitter activity, such as the release of acetylcholine, dopamine and noradrenaline 18). In addition, phosphatidylserine-omega-3 was found to significantly increase DHA level in brains of middle-aged rats 19).

Mammalian cell membranes contain >1,000 different phospholipids 20). Phosphatidylcholine is the most abundant phospholipid in mammalian cell membranes, constituting 40–50% of total phospholipids. The second most abundant mammalian membrane phospholipid is phosphatidylethanolamine (PE), which constitutes 20–50% of total phospholipids. In the brain, ∼45% of total phospholipids are phosphatidylethanolamine, whereas in the liver, only ∼20% of total phospholipids are phosphatidylethanolamine. Phosphatidylserine is a quantitatively minor membrane phospholipid that makes up 2–10% of total phospholipids.

In the plasma membrane, phosphatidylserine is localized exclusively in the cytoplasmic leaflet where it forms part of protein docking sites necessary for the activation of several key signaling pathways. These include the Akt, protein kinase C (PKC) and Raf-1 signaling that is known to stimulate neuronal survival, neurite growth and synaptogenesis 21). Modulation of the phosphatidylserine level in the plasma membrane of neurons has significant impact on these signaling processes. The mechanism of phosphatidylserine-mediated activation of these neuronal signaling pathways is illustrated in Figure 2.

Figure 1. Phosphatidylserine

phosphatidylserine

Figure 2. Activation of neuronal signaling pathways facilitated by phosphatidylserine

Activation of neuronal signaling pathways facilitated by phosphatidylserine

Footnotes: Activation of neuronal signaling pathways facilitated by phosphatidylserine. Activation of Akt, protein kinase C and Raf-1 requires translocation from the cytosol to the cytoplasmic surface of the plasma membrane. Translocation is initiated by specific stimuli, for example, growth factor-dependent PIP3 generation from PIP2 by PI3 kinase in the case of Akt. Binding to the membrane occurs in part through an interaction of these proteins with phosphatidylserine present in anionic domains of the lipid bilayer, activating the signaling pathways leading to neuronal differentiation and survival. DHA facilitates this mechanism by increasing phosphatidylserine production in neurons, while ethanol has the opposite effect because it inhibits the DHA-induced increase in PS production.

Abbreviations: PS =phosphatidylserine; R = receptor; DHA = docosahexaenoic acid; PC = phosphatidylcholine; PE = phosphatidylethanolamine

[Source 22)]

Phosphatidylserine biological function

Phosphatidylserine, a phospholipid with a negatively charged head-group, is an important constituent of eukaryotic cellular membranes. On the plasma membrane, rather than being evenly distributed, phosphatidylserine is found preferentially in the inner leaflet. Disruption of this asymmetry, leading to the appearance of phosphatidylserine on the surface of the cell, is known to play a central role in both apoptosis and blood clotting.

The best-studied roles of phosphatidylserine involve signalling, not within the intracellular environment, but in an extracellular context such as during apoptosis 23) and during blood clotting. Like most lipids, phosphatidylserine is not evenly distributed throughout all cellular membranes, nor is it always equally distributed between leaflets of a membrane bilayer 24). In healthy cells plasmalemmal phosphatidylserine is exclusively on the inner (cytoplasmic-facing) leaflet due to the action of ATP-dependent aminophospholipid flippases 25). When cells undergo apoptosis (regulated cell death) phosphatidylserine appears on the outside-facing (extracellular) leaflet, signalling phagocytic cells to engulf the dying cell. phosphatidylserine is also exposed exofacially in activated blood platelets, which prompts the binding and activation of a number of clotting factors, including factors V, VIII, X and prothrombin 26).

There is little doubt that, in addition to these extracellular functions, phosphatidylserine plays important roles within the intracellular environment. Indeed, a number of important intracellular proteins require phosphatidylserine for their proper localization and/or activation. Such proteins include the E3 ubiquitin-protein ligase NEDD4, a number of protein kinase C isoforms, several phospholipase C and D isoforms, PTEN ,an important phosphatidylinositol (3,4,5)-trisphosphate phosphatase, dysferlin, a protein important in muscle repair, as well as a number of synaptotagmin isoforms that are important for vesicular trafficking and fusion 27). Additionally, it is known on the whole that phosphatidylserine is important, as mice with a complete loss of ability to synthesize phosphatidylserine are not viable 28), and though yeast are able to survive without phosphatidylserine synthesis, their growth is greatly impaired 29). However, despite the obvious importance of intracellular phosphatidylserine, its distribution, dynamics and function have not been thoroughly investigated.

Cell signaling

Phosphatidylserine(s) are actively held facing the cytosolic (inner) side of the cell membrane by the enzyme flippase. However, when a cell undergoes apoptosis, phosphatidylserine is no longer restricted to the cytosolic side by flippase. Instead scramblase catalyzes the rapid exchange of phosphatidylserine between the two sides. When the phosphatidylserines flip to the extracellular (outer) surface of the cell, they act as a signal for macrophages to engulf the cells 30).

Coagulation

Phosphatidylserine plays a role in blood coagulation (also known as clotting). When circulating platelets encounter the site of an injury, collagen and thrombin -mediated activation causes externalization of phosphatidylserine from the inner membrane layer, where it serves as a pro-coagulant surface 31). This surface acts to orient coagulation proteases, specifically tissue factor and factor VII, facilitating further proteolysis, activation of factor X, and ultimately generating thrombin 32).

In the coagulation disorder Scott syndrome, the mechanism in platelets for transportation of phosphatidylserine from the inner platelet membrane surface to the outer membrane surface is defective 33). It is characterized as a mild bleeding disorder stemming from the patient’s deficiency in thrombin synthesis 34).

Ethanol-induced effects

Findings in cultured neuronal cells and animal models indicate that ethanol can disrupt the beneficial interaction between DHA and phosphatidylserine. Exposure of Neuro 2A cells to 25 mM ethanol decreased the DHA-mediated accumulation of phosphatidylserine, Akt phosphorylation and cell survival as indicated in Figure 2 above. Administration of ethanol to pregnant rats also decreased the DHA and phosphatidylserine content of the fetal hippocampus and increased the number of apoptotic hippocampal cells 35). Likewise, administration of ethanol to rats during the prenatal and developmental period decreased microsomal phosphatidylserine biosynthetic activity without altering phosphatidylserine synthetase expression, and thus the amount of phosphatidylserine, particularly the 18:0, DHA species in the cerebral cortex 36). The ethanol-mediated decrease in the 18:0, DHA-phosphatidylserine molecular species is also consistent with the finding that incubation of brain microsomes with high concentrations of ethanol increased oleoyl-CoA incorporation into phosphatidylserine and diverted polyunsaturated fatty acids into triglycerides 37). Considering the significant roles played by phosphatidylserine in neuronal survival and function discussed above, a reduction in DHA-stimulated synthesis of phosphatidylserine may be one factor that produces the deleterious effect of ethanol on the central nervous system.

Phosphatidylserine foods

Phosphatidylserine is commonly found in common foods such as meat, fish and legumes,. Currently, dietary intakes of phosphatidylserine, from its natural presence in the diet, is estimated to be in the range of 75 – 184 mg/person/day.

Table 1. Phosphatidylserine content in different foods

FoodPhosphatidylserine Content in mg/100 g
Bovine brain713
Atlantic mackerel480
Chicken heart414
Atlantic herring360
Eel335
Offal (average value)305
Pig’s spleen239
Pig’s kidney218
Tuna194
Chicken leg, with skin, without bone134
Chicken liver123
White beans107
Soft-shell clam87
Chicken breast, with skin85
Mullet76
Veal72
Beef69
Pork57
Pig’s liver50
Turkey leg, without skin or bone50
Turkey breast without skin45
Crayfish40
Cuttlefish31
Atlantic cod28
Anchovy25
Whole grain barley20
European hake17
European pilchard (sardine)16
Trout14
Rice (unpolished)3
Carrot2
Ewe’s Milk2
Cow’s Milk (whole, 3.5% fat)1
Potato1
[Source 38)]

Phosphatidylserine synthesis in the brain

In mammalian tissues, phosphatidylserine is synthesized from either phosphatidylcholine or phosphatidylethanolamine exclusively by Ca2+-dependent reactions where the head group of the substrate phospholipids is replaced by serine 39), as illustrated in Figure 3. These base-exchange reactions are catalyzed by phosphatidylserine synthases (PSS) and so far two isoforms, PSS1 and PSS2 encoded by two separate genes, Pss1 and Pss2, respectively, have been identified. PSS1 utilizes phosphatidylcholine as its substrate, and PSS2 utilizes phosphatidylethanolamine. These enzymes are localized in the endoplasmic reticulum, particularly enriched in the mitochondria associated membrane regions of the endoplasmic reticulum 40).

Together with testis and kidney, brain is one of the tissues that have high capacity to synthesize phosphatidylserine 41). Also, the expression of phosphatidylserine synthases (PSS) in the brain is among the highest. The serine base exchange enzymatic activities of rat cerebellar homogenates, cerebral cortical homogenates and cerebral cortical membranes were shown to be recovered in the insoluble floating fraction of TritonX-100 extracts, suggesting the localized presence of phosphatidylserine synthases in membrane lipid rafts 42). Although intriguing, the possible contribution of microsomal contamination cannot be excluded. Phosphatidylserine production is increased in cells of neuronal origin by compounds that trigger Ca2+ release, a finding consistent with the fact that phosphatidylserine synthesis is a Ca2+-dependent process 43).

Figure 3. Phosphatidylserine synthesis and metabolism in the brain

phosphatidylserine synthesis and metabolism in the brain

Footnotes: Phosphatidylserine synthesis and metabolism in the brain. Phosphatidylserine is synthesized by replacement of the choline group of phosphatidylcholine by serine in a reaction catalyzed by phosphatidylserine synthase 1, and also by replacement of the ethanolamine group of phosphatidylethanolamine by serine in a reaction catalyzed by phosphatidylserine synthase 2. These synthetic reactions occur in the endoplasmic reticulum. phosphatidylserine is decarboxylated to phosphatidylethanolamine in the mitochondria by phosphatidylserine decarboxylase (PSD). The phosphatidylethanolamine methyltransferase (PEMT) reaction that utilizes S-adenosylmethionine (SAM) to convert phosphatidylethanolamine to phosphatidylcholine is indicated as a dashed arrow because more recent findings have demonstrated that previously reported methylation activity in the brain is quantitatively insignificant 44).

Abbreviations: PC = phosphatidylcholine; PE = phosphatidylethanolamine; PS = phosphatidylserine; PSD = phosphatidylserine decarboxylase; PSS = phosphatidylserine synthases

[Source 45)]

Composition of brain phosphatidylserine

The phosphatidylserine content in human brain is maintained at the 13–14% level throughout the life 46). The fatty acid composition of phosphatidylserine, and for comparison that of phosphatidylethanolamine and phosphatidylcholine, contained in the gray and white matter of human brain, is shown in Table 2 47). There are substantial differences in the fatty acid composition in gray and white matter phosphatidylserine. Gray matter phosphatidylserine contains considerably more DHA and less 18:1n-9 than white matter. Appreciable differences also occur in the phosphatidylethanolamine fatty acid composition in gray and white matter, whereas comparatively small differences occur in the phosphatidylcholine composition. Docosahexaenoic acid (DHA) accounts for more than one-third of the total fatty acid and 80% of the polyunsaturated fatty acid in gray matter phosphatidylserine. A substantial amount of DHA is present in gray matter phosphatidylethanolamine, but only a relatively small amount is present in phosphatidylcholine. Gray matter phosphatidylserine and phosphatidylethanolamine contain considerably more 18:0 and much less 16:0 than phosphatidylcholine. Arachidonic acid is present primarily in phosphatidylethanolamine, and there is little arachidonic acid in phosphatidylserine. According to one study 48), phosphatidylethanolamine also contains the largest amount of docosapentaenoic acid, an arachidonic acid-derived product. Only trace amounts of linoleic acid (18:2n-6) are present in brain phosphatidylserine, phosphatidylethanolamine and phosphatidylcholine.

Table 2. Fatty acid composition of human brain glycerophosphatides

Fatty acidFatty Acyl Composition (% of total fatty acid in each phospholipid class)
PhosphatidylserinePhosphatidylethanolaminePhosphatidylcholine
Gray matterWhite matterGray matterWhite matterGray matterWhite matter
AaBbABABABABAB
16:02.34.21.71.96.75.76.73.445.045.934.330.2
16:10.30.30.40.30.40.41.40.53.12.41.02.3
18:025.445.335.844.126.028.49.09.39.311.213.412.9
18:121.514.039.741.411.910.342.438.931.430.345.247.1
20:41.63.02.01.213.811.26.416.54.13.61.30.8
22:5n-65.00.74.80.114.31.213.70.7ndctrdnd0.2
22:5n-33.30.50.90.2tr1.10.50.9ndtr0.30.3
22:636.623.25.61.324.330.53.48.63.12.50.10.2
[Source 49)]

Interactions between phosphatidylserine and DHA

Brain is enriched with DHA (docosahexaenoic acid), and the phosphatidylserine content in the grey matter of human brain is particularly high as shown in Table 1. Phosphatidylcholine and phosphatidylethanolamine containing DHA are the best substrate for phosphatidylserine biosynthesis 50). As a consequence, the phosphatidylserine level is high in the brain where DHA is abundant. In contrast, DHA-depletion from the brain lowers the phosphatidylserine level 51). For example, dietary depletion of Omega-3 fatty acids can reduce DHA in the brain and increase the Omega-6 counterpart docosapentaenoic acid. Since phospholipids containing docosapentaenoic acid are not as good substrates for phosphatidylserine synthesis as DHA (docosahexaenoic acid)-containing phospholipid species, the brain phosphatidylserine level is reduced 52). It is important to note that modern western diets are excessively abundant in Omega-6 fatty acids compared to Omega-3 fatty acids, and therefore, DHA enrichment in the brain is compromised as indicated by the considerable accumulation of docosapentaenoic acid observed in the postmortem human hippocampus 53). Such a fatty acid profile is comparable to that observed in rodent brains depleted in DHA at least to a moderate extent, and therefore, the phosphatidylserine level is likely not at a maximum in modern human brains although systematic analysis has not yet been performed.

Phospahtidylserine and cognitive function

A decrease of the DHA content in phosphatidylserine has been reported in cognitive impairment. A small reduction in the DHA content of hippocampal phosphatidylserine was observed in 12 month-old senescence-accelerated prone mice that have a shorter life span, learning and memory deficit, and an increase in hippocampal Aβ-peptide content 54). The decrease in DHA was associated with a corresponding increase in the AA content of hippocampal phosphatidylserine. Likewise, the DHA content of phosphatidylserine in the superior temporal and mid-frontal cortex was reduced by 12 and 14 %, respectively, in brain tissues obtained from patients with Alzheimer’s disease 55). However, there is no information as to how a decrease in the DHA content of phosphatidylserine might contribute to the pathogenesis of cognitive impairment, and a decrease in DHA content is not a uniform finding in animal models of cognitive impairment. For example, substantial fatty acyl compositional changes, including reductions in AA, have been observed in brain phosphatidylserine of aged Wistar rats with cognitive deficits, but there is no difference in the DHA content of the phosphatidylserine 56). Therefore, the putative linkage between DHA reductions in phosphatidylserine and cognitive impairment remains open to question.

Effects of dietary phosphatidylserine supplements on cognitive function

Dietary phosphatidylserine supplements are reported to improve cognitive function in experimental animals 57), and a similar result has been obtained recently with krill phosphatidylserine which has a high content of omega-3 fatty acid. Aged rats given daily doses of krill phosphatidylserine orally for 7 days showed improvement in the Morris water maze test. There was less loss of choline acetyltransferase and acetylcholine esterase transporter mRNA in the hippocampus. The neuroprotective activity of 20 mg/kg krill phosphatidylserine was equivalent to that of 50 mg/kg soy phosphatidylserine in these aged rats 58). Normal young rats given 100 mg/kg krill phosphatidylserine orally for 30 days also showed improvement in the Morris water maze test 59).

Likewise, cognitive improvement was reported in humans given oral phosphatidylserine supplements 60), and these findings subsequently were confirmed and extended. Human subjects treated for 42 days with 200 mg of soy-based phosphatidylserine showed a more relaxed state before and after mental stress as measured by electro-encephalography 61), and no adverse effects were evident at this dose given three-times a day for 6 to 12 weeks 62). The ability to recall words increased by 42% in male and female subjects who were older than 60 years and complained of subjective memory loss when they were treated with 300 mg/day of phosphatidylserine containing 37.5 mg of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) 63). Improved verbal immediate recall was also observed in a double-blind, placebo controlled clinical trial in a large group of elderly subjects with memory complaints when treated with a daily dose of 300 mg phosphatidylserine containing DHA and eicosapentaenoic acid in a 3:1 ratio. A subset with relatively good cognitive performance at baseline showed the greatest improvement 64). In a similar double blind study in Japanese subjects between the ages of 50 and 69 years with memory complaints, subjects having low scores at baseline showed greater improvement in delayed verbal recall after treatment for 6 months with soybean phosphatidylserine 65).

Several biochemical responses to phosphatidylserine administration that have been reported in experimental animals could be involved in the mechanism of phosphatidylserine-mediated improvement in cognition. Stimulation of dopamine-dependent adenylate cyclase activity was observed in mouse brain following an intravenous infusion of a sonicated preparation of bovine brain phosphatidylserine 66). Sonicated suspensions of phosphatidylserine injected intravenously also increased calcium-dependent acetylcholine output from the cerebral cortex in urethane anesthetized rats 67). Likewise, intravenous injection of purified bovine brain phosphatidylserine for 8 days attenuated the decrease in acetylcholine release from the parietal cortex in aged rats, possibly by providing more choline for acetylcholine synthesis 68). Furthermore, orally administered krill phosphatidylserine in normal young rats for 30 days produced an increase in neurons positive for brain-derived neurotrophic factor and insulin-like growth factor in the hippocampal CA1 region 69).

A current hypothesis is that these biochemical responses and the resulting cognitive improvements are due to phosphatidylserine mediated effects on neuronal membrane properties 70). However, experimental evidence indicating that orally or intravenously administered phosphatidylserine actually alters neuronal membrane properties is lacking. How the administered phosphatidylserine is transported in the plasma, how much enters the brain, whether it is taken up intact, and whether it is incorporated into neurons or glia are not known. Dietary phospholipids are hydrolyzed during digestion, so orally administered phosphatidylserine most likely is not absorbed intact. Phosphatidylserine preparations are rich in DHA, and DHA supplementation is known to improve hippocampal function 71). Because the administered phosphatidylserine probably undergoes partial or complete hydrolysis, the beneficial effects of phosphatidylserine on cognition, particularly from krill or bovine sources, possibly are produced by DHA released from the phosphatidylserine rather than the intact phosphatidylserine itself. These issues will have to be investigated in order to obtain some mechanistic insight into how dietary or intravenously administered phosphatidylserine supplements function to produce cognitive improvement.

Phosphatidylserine summary

A body of evidence supports the functional significance of phosphatidylserine in the brain. Underlying mechanisms are still unfolding; however, phosphatidylserine facilitates the activation of signaling proteins and receptors that are critical for neuronal survival, differentiation and synaptic neurotransmission. Despite its constitutive nature, membrane phosphatidylserine is often an indispensable participant in signaling events and/or influences the signaling in a concentration-dependent manner. The phosphatidylserine biosynthesis preferentially utilizes DHA-containing phospholipids as substrates. Although membrane phospholipids are under a tight homeostatic regulation, the phosphatidylserine level can be altered according to the DHA status, specifically in the brain. Therefore, diet- or ethanol-induced alteration of the brain DHA level and membrane phosphatidylserine can influence the signaling platform in the membrane and the transmission of the signaling cues. Detailed molecular mechanisms, particularly membrane phosphatidylserine-protein interactions, warrant further investigation in order to obtain more insight into the functional significance of neuronal phosphatidylserine. Such endeavor is likely to generate new targets for controlling physiologic or pathophysiologic processes affecting brain function.

Phosphatidylserine dosage

A typical recommended dose of phosphatidylserine as a dietary supplement is 100 mg three times a day (300 mg/day). In numerous human clinical studies, the safety of phosphatidylserine has been confirmed at daily doses of up to 300 mg for up to 6 months 72). The safety of phosphatidylserine has been proven in human clinical studies including susceptible groups (elderly and children) and healthy individuals.

Phosphatidylserine side effects

Phosphatidylserine has been marketed as a dietary supplement for the past two decades without any adverse effects (except gastrointestinal side effects such as nausea and indigestion). A variety of animal toxicity studies and in vitro mutagenicity/genotoxicity studies corroborate the human clinical safety data. The animal studies did not show any significant toxicity at doses up to approximately 1,000 mg/kg/day 73).

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