Dietary deficiency of docosahexaenoic acid (C22: 6n-3; DHA) is linked to the neuropathology of several cognitive disorders, including anxiety. DHA, which is essential for brain development and protection, is primarily obtained through the diet or synthesized from dietary precursors, however the conversion efficiency is low. Curcumin (diferuloylmethane), which is a principal component of the spice turmeric, complements the action of DHA in the brain, and this study was performed to determine molecular mechanisms involved. We report that curcumin enhances the synthesis of DHA from its precursor, α-linolenic acid (C18: 3n-3; ALA) and elevates levels of enzymes involved in the synthesis of DHA such as FADS2 and elongase 2 in both liver and brain tissue. Furthermore, in vivo treatment with curcumin and ALA reduced anxiety-like behavior in rodents. Taken together, these data suggest that curcumin enhances DHA synthesis, resulting in elevated brain DHA content. These findings have important implications for human health and the prevention of cognitive disease, particularly for populations eating a plant-based diet or who do not consume fish, a primary source of DHA, since DHA is essential for brain function and its deficiency is implicated in many types of neurological disorders.

Turmeric (Curcuma Longa) is native to Southeast India, and the yellow curry spice derived from the plant is a staple in Indian cooking. Ironically, DHA is poorly consumed in India based on the vegetarian prevalence in the population. Turmeric contains the polyphenolic secondary metabolite curcumin, which has been implicated to improve brain health including reducing degeneration in Alzheimer’s disease [ 19 , 37 – 39 ], ischemia [ 40 ] and traumatic brain injury [ 22 , 41 – 43 ]. In addition to having profound antioxidant and anti-inflammatory effects in various tissues [ 44 ][ 45 ][ 46 ][ 47 ][ 48 ][ 49 ][ 50 ], we recently showed that curcumin prevents reduced DHA content in the brain following brain trauma, benefiting brain plasticity as well as reducing oxidative damage [ 22 ]. Additionally, while curcumin + DHA had additive beneficial effects on plasticity, behavior and brain DHA content, the combined supplementation with curcumin + DHA reduced brain content of the DHA precursor n-3 DPA, raising the question as to whether curcumin stimulates the synthesis of DHA [ 22 ]. Therefore, the standing question is what are the molecular mechanisms by which curcumin would support the action of DHA on brain function and plasticity under homeostatic conditions. Here we explore the possibility that curcumin increases the production of DHA by influencing precursors such ALA and DPA.

Omega-3 fatty acids require n-3 fatty acid precursors for de novo synthesis in mammals and therefore n-3 fatty acids must be obtained through the diet. The n-3 fatty acids DHA and eicosapentaenoic acid EPA (C20: 5n-3) can be obtained directly from animal sources or can be synthesized from plant derived n-3 fatty acid precursors. Primary sources of DHA are fish and seafood. Sources of the precursor for DHA and EPA: α-linolenic acid (C18:3 n-3; ALA) include sunflower and soybean oil (> 50% of the fat) [ 28 ]. DHA synthesis from its precursors ALA, EPA and docosapentaenoic acid (C22:5 n-3; DPA) mainly takes place in the liver since the synthesis of DHA in the brain is very limited [ 29 ]. In general, the conversion efficiency of DHA synthesis from ALA is quite low [ 30 – 32 ]. Vegetarians and vegans thus have reduced plasma DHA compared to omnivores [ 33 – 36 ], yet many populations thrive on an entirely plant based diet and are able to obtain adequate levels of DHA to support cognitive development and plasticity. This raises the question as to whether other food components commonly obtained in the vegetarian diet might enhance the conversion of DHA from n-3 precursors. There is a discrepancy between animal studies showing cognitive impairment associated with DHA deficiency and human data reporting vegetarians have normal cognitive abilities. We conducted an investigation asking whether components commonly consumed in traditional vegetarian diets could enhance DHA content in the brain and the synthesis of DHA from plant-based sources.

Docosahexaenoic acid (DHA, C22: 6n-30) is the most prevalent omega 3 (n-3) fatty acid in brain tissue, and its deficiency is linked to several neurocognitive disorders such as anxiety-like behavior [ 1 , 2 ], Alzheimer’s disease [ 3 ], major depressive disorder [ 4 ], schizophrenia [ 5 ] with psychosis [ 6 ] and impaired attention [ 7 , 8 ]. Extensive reports using rodent models have identified that deficiency of DHA during growth and development causes significant learning and memory impairments [ 2 , 9 – 12 ]. In addition to being critical for brain development [ 13 – 17 ] dietary DHA is particularly important during challenging situations such as aging [ 18 – 21 ], or brain injury [ 22 , 23 ]. Notably, low levels of DHA are associated with generalized anxiety [ 4 ] and supplementation with DHA has been shown to have anxiolytic effects [ 24 – 27 ]. Thus, n-3 fatty acids play a critical role in brain health and the overall prevention of cognitive disease.

We treated cultured liver cells HepG2 with the DHA precursor n-3 DPA (50 μM) or DPA plus three different doses of CUR (10, 20, or 40μM). In an initial experiment we treated the cells with the precursor ALA + curcumin, however we found that in cultured liver cells ALA + curcumin did not increase synthesis of DHA (data not shown). Similar findings were previously reported indicating that treating cultured HepG2 cells with ALA does not increase DHA synthesis [ 52 ]. The lack of existing fatty acid precursors such as DPA, which are present in an in vivo study, cause FADS2 to preferentially bind to ALA, thus levels of EPA and DPA accumulate while the final conversion from DPA → DHA is negligible [ 52 ]. The conversion of DPA → DHA by FADS2 is the rate-limiting step in DHA synthesis from ALA, therefore for our in vitro study cells were treated with DPA. The combination of DPA + CUR (20μM) significantly increased DHA levels (132% of VEH) compared to DPA treatment alone (p<0.05; ). Lower doses of CUR at doses of 10 μm did not have effects on DHA synthesis while the higher dose tended to reduce DHA levels to 85% of VEH and significantly reduced DHA synthesis compared to the 20μM dose. These results suggest that CUR has a dose specific effect on the conversion of n-3 DPA to DHA. Protein levels of FADS2 and Elov2 were elevated by CUR + DPA at all measured doses ( ). Similar to the DHA content, the 20 μM dose caused a large increase in FADS2 (175% of VEH; p<0.05; ) which was significantly greater than the 10 μM dose (p<0.05), and tended to be higher than the 40 μM dose. All doses of CUR caused a greater increase in FADS2 compared with VEH or DPA alone ( ). Similarly, DPA + CUR increased the levels of Elov2 at all three doses (p<0.05; ). Finally, we sought to determine the role of FADS2 on the process underlying CUR-enhanced DHA synthesis. Cultured HepG2 cells were pre-treated with the FADS2 inhibitor SC-26196 (2 μM) prior to adding DPA (50 μM) + CUR (20 μm) to the culture media. The FADS2 inhibitor SC-26196 significantly reduced DHA levels in cells treated with DPA plus CUR (69% of DPA + CUR control group p<0.05; ). Together these findings suggest that CUR promotes hepatic DHA synthesis, in which the desaturase FADS2 plays a critical role.

Since DHA is mainly synthesized in the liver, we sought to determine the effects of CUR on hepatic DHA. Compared with CTL, ALA alone increased DHA in the liver (136% of control, p>0.05; ). CUR alone did not affect DHA content in the liver (p>0.05; ), however hepatic DHA was significantly increased when CUR was combined with ALA (171% of CTL for 500 the ppm dose, 179% of CTL for the 250 ppm dose, p<0.05; ). We measured levels of the enzymes FADS2 and Elov2 in liver to evaluate effects of CUR on enzymes involved in hepatic DHA synthesis. CUR 500ppm + ALA significantly increased the levels of FADS2 (132% of CTL, p<0.05; ), whereas CUR + 250ppm further elevated FADS2 (161% of CTL) significantly more than the CUR 500ppm group (p<0.05; ). CUR alone or in combination with ALA significantly elevated the levels of Elov2 (123% or 120% of control, respectively; p<0.05; ). Similar to FADS2, CUR 250ppm had greater Elov2 (159% of CTL) compared to CUR 500ppm (p<0.05; ). Together these findings suggest that CUR may enhance the conversion of ALA to DHA in the liver. CUR alone did not reduce levels of the lipid peroxidation product 4 HNE, however in combination with ALA levels of 4 HNE were significantly reduced compared with CTL and CTL+CUR. ALA alone also reduced levels of 4-HNE compared with CTL and there was a trend toward further reduction when ALA was combined with CUR 250 or CUR 500 (p=0.1 and 0.2, respectively; ). Levels of n-3 and n-6 fatty acids were quantified in liver and are presented in . In the liver, ALA, CUR and ALA+CUR 250ppm did not significantly affect C18:2 n-6 or C20:3n-6 but significantly reduced levels of 20:4n-6. Both CUR and ALA reduced C22:5n-6 relative to CTL, whereas levels of C22:5n-3 were increased by ALA and in both ALA+CUR groups, though CUR+CTL had no effect. Compared with CTL, ALA and CTL+CUR 22:6 n-3 was significantly increased in both CUR+ALA groups. We sought next to corroborate the action of these enzymes on the effects of CUR in isolated liver cells in culture.

Animals were maintained on a diet supplemented with ALA (2.7% of total fatty acids) or ALA+CUR (250 or 500 ppm). ALA alone or CUR alone did not increase DHA content in the hippocampus compared to control group (p>0.05; ). However, when rats were fed ALA+CUR, DHA content was significantly higher (162 or 152% of CTL for 250 or 500 ppm curcumin-fed animals, respectively) in ALA+CUR than ALA alone group (p<0.05; ). These findings suggest that CUR may enhance the conversion of ALA to DHA in vivo and elevate DHA content in brain. We assessed the relevance of the dietary intervention on cognitive function using the elevated-plus maze, a measure of anxiety-like behavior. We found that the time spent in the open arm was significantly higher in ALA+CUR groups compared with ALA or CUR alone or CTL (p<0.05; ). We regressed DHA% of CTL measured in the hippocampus against elevated plus maze scores and found a significant positive correlation between brain DHA levels and time spent in the open arms, indicating that DHA in the brain is associated with reduced anxiety-like behavior (p<0.05; ). We quantified enzymes involved in the synthesis of DHA from n-3 precursors in brain tissue using immunoblotting. The enzyme FADS2 is involved in the desaturation process during the conversion of precursor ALA to DHA. Elov2 is involved in the elongation steps during DHA synthesis. In the brain we found that CUR alone increased levels of FADS2 (126% of control, p<0.05; ), and the presence of ALA in the diet increased the effects of CUR at 500 ppm on FADS2 (150% of control, p<0.05; ), whereas ALA alone did not affect FADS2 levels. Though significantly elevated compared to CTL, CUR at a dose of 250ppm with ALA led to lower FADS2 (120% of CTL, p<0.05) compared to the CUR 500ppm + ALA treatment group ( ). CUR (500ppm) also significantly elevated the levels of Elov2 when provided alone (114% of control, p<0.05) or in combination with ALA (132% of control, p<0.05; ). CUR at dose of 250ppm + ALA led to lower Elov2 (105% of CTL, p<0.05) compared to ALA + CUR at a dose of 500 ppm (p<0.05; ). The enzymes FASD2 and Elov2 are involved in synthesis of n-6 fatty acids as well as n-3 fatty acids. shows levels of n-3 and n-6 fatty acids quantified in brain tissue. The intermediates 18:2 n-6, 20:3 n-6 and 20:4 n-6 were elevated by CUR + ALA at the 250 ppm dose relative to CTL. Notably, 20:4n-6 was elevated at both doses of CUR + ALA relative to controls, however the n-6 end product 22:5n-6 was not elevated by curcumin treatment whereas 22:6 n-3 was elevated in both groups. The n-3 EPA and DPA are not pictured because levels were too low for detection using our methods. Curcumin has known antioxidant and anti-inflammatory activities, thus it is possible that the effects of CUR + ALA are due to neuroprotective effects of CUR rather than a direct product of enhanced DHA synthesis. We sought to determine whether curcumin in the diet affects markers of lipid peroxidation using as a marker the lipid degradation product 4 hydroxynonenol (4-HNE). Curcumin alone did not affect levels of 4-HNE, however there was a significant reduction in 4-HNE in animals fed ALA, which was further elevated with the addition of CUR to the diet ( .) Taken together these findings suggest that dietary CUR, when combined with the ALA precursor, increases DHA in the brain, reduces anxiety-like behavior and that CUR increases the quantity of DHA processing enzymes in the hippocampus.

Total lipids were extracted from cerebral tissues or cultured cells with lysis solution of chloroform-methanol (2:1, vol:vol) containing 0.005% Butylated hydroxytoluene in a ratio of sample to lysis solution of 1:20 (i.e. 100 mg tissue + 2ml lysis solution). Samples were homogenized and extracted overnight at 4°C, then centrifuged for 5 min at 1200×g and the supernatant was aspirated and transferred to a new tube. 1 mL of lysis solution was added to the pellet and the centrifugation was repeated and supernatant collected. To the combined supernatant solution, 0.2 mL 0.9 % sodium chloride solution was added and the liquid centrifuged at 2170×g for 15 min at 4°C. The chloroform layer was transferred to a new 15 ml tube, and then mixed with an additional 0.2 mL 0.9% saline. After centrifugation again for 10 min at 2170×g at 4°C, the chloroform layer was transferred to another 15 ml tube and evaporated under nitrogen gas. The sample of total lipids was dissolved in 1 mL hexane and methylated by 14% boron trif luoride–methanol reagent (1 mL) at 90°C for 1 hour. Oxygen was displaced using nitrogen gas. After cooling to 21°C 1 mL of distilled deionized water was added and samples were vortexed and allowed to sit for 30 min to separate the water from the organic layer. The organic layer was transferred to a new tube and evaporated using nitrogen gas. Fatty acid profiles were determined by using gas chromatography (GC). The system consisted of model Clarus 500 gas chromatograph (PerkinElmer) with a built-in Autosampler. An Elite-WAX column (60m, 0.32-mm internal diameter, PerkinElmer) was used, with hydrogen as the carrier gas. GC oven temperature was initially held at 140 °C for 2 min and raised with a gradient of 5 °C min −1 until 250 °C and held for 10 min. The total run time is 34 min. The injector and detector were maintained at 250 and 300 °C, respectively. A 1μl sample of fatty acid methyl esters (FAME) was injected in split injection mode with a 100:1 split ratio. Peaks of resolved fatty acid methyl esters were identified and quantified by comparison with standards (Supelco 37-component FAME Mix).

The total proteins from hippocampus were extracted. Protein samples were separated by electrophoresis on an 8% polyacrylamide gel and electrotransferred to a nitrocellulose membrane. Non-specific binding sites were blocked in TBS, overnight at 4°C, with 2% BSA and 0.1% Tween-20. Membranes were rinsed for 10 min in buffer (0.1% Tween-20 in TBS) and then incubated with anti-FADS2, anti-Elov2 (elongase 2), anti-4HNE and anti-β-actin (1:1000, Santa Cruz Biotechnology, Santa Cruz, CA), followed by anti-goat or anti-rabbit IgG horseradish peroxidase-conjugate (Santa Cruz Biotechnology, Santa Cruz, CA). Immunocomplexes were visualized by chemiluminescence using an ECL kit (Amersham Pharmacia Biotech Inc., Piscataway, NJ) according to the manufacturer’s instructions. The film signals were digitally scanned and then quantified using NIH Image software.

The elevated plus maze (EPM) test was performed as described by Walf and Frye [ 51 ]. Briefly, the EPM apparatus is made of laminated wood consisting of 2 opposing open arms (10×50 cm) and 2 opposing closed arms (10×50 cm with 30 cm high walls). The maze was placed 60 cm above the floor and enclosed with curtains. An overhead video camera was used to record behavior over a period of 5 min. Each rat was placed in the middle of the maze pointed toward the open arm that faced away from the experimenter. The time spent and the number of entries into each arm was recorded using AnyMaze video tracking software (San Diego Instruments, San Diego, CA). Data are reported as time spent in the open arm (seconds).

After 1 week acclimatization on standard chow, the rats (n=5–6/group) were fed control diet (CTL), ALA diet (ALA; 2.7% of fat), curcumin diet (CUR, 500ppm), or ALA + CUR diet (ALA, 2.7% of fat; CUR, 500 ppm). The diet components, including fatty acid profiles are shown in . Diets were custom made (Dyets Inc., Bethlehem, PA) and provided to animals in powder ad libitum. After 3.5 weeks of feeding of the respective diet, rats were sacrificed by decapitation, and brains were rapidly dissected out, frozen on dry ice, and stored at −70°C until use for biochemical analyses. One half of each brain was used for immunoblotting and the other half for lipids analysis.

Discussion

We report novel data showing that curcumin elevates DHA synthesis from n-3 precursors in liver cells, and that in combination with dietary ALA, curcumin increases DHA content in vivo in both the liver and brain. Enzymes involved in the synthesis of DHA, FADS2 and elongase 2, were concurrently elevated, suggesting that curcumin may increase DHA content, in part, by increasing the pool of enzymes available to facilitate the conversion from either ALA or DPA. In the liver, dietary ALA elevated the DHA precursor n-3 DPA, whereas curcumin did not increase levels of this precursor ( ). In support of this, we found that inhibition of the FASD2 enzyme in liver cells attenuated increases in DHA content associated with the combined treatment with DPA and curcumin. In this study, we also report that elevated DHA content in the brain associated with curcumin and ALA in the diet correlates with reduced anxiety-like behavior. These findings have important implications for human health and the prevention of cognitive disease, particularly for populations eating a plant-based diet or who do not consume fish, a primary source of DHA, since DHA is essential for brain function and its deficiency is implicated in many types of neurological disorders.

Structurally, DHA accounts for roughly one third of the fatty acids in the gray matter of the brain and is essential to normal healthy brain development [13–17]. Dietary deficiency of n-3 fatty acids during developmental years has detrimental effects on cognitive abilities [10, 11, 53–55], but cognitive performance can be improved by increasing brain DHA content [55]. Animal studies strongly suggest that dietary deficiency of DHA increases the risk for neurocognitive disorders [56, 57], and that diets enriched with DHA fosters learning and memory [18, 58–62] and are protective against cognitive decline during aging [18, 20]. In humans, circulating DHA is significantly related to cognitive abilities during aging [63] and inversely associated with cognitive decline [64].

While DHA can be obtained through animal sources in the diet, vegetarians and vegans may face challenges getting adequate dietary DHA [35]. Increasingly, vegetarianism and veganism is being adopted in the Western world [65]. Circulating omega 3 fatty acids are lower in vegetarians and non-fish eaters than in people who consume fish [66]. Furthermore, changes in farming practices and food consumption have taken place over the last century such that the dietary n-3 fatty content may be declining [67]. For example, aquaculture currently accounts for nearly one half of the seafood supply for human consumption in the world, which is large increase compared with 1980’s, where aquaculture contributed only 9% or even 2000 where fisheries made up 34% [68]. Terrestrial oilseeds [69] and maize [70] are commercially used in fish feed, which can increase the ratio of n-6:n-3 in seafood [71–74]. Other dietary sources of DHA, such as beef [75] and eggs [76] have reduced DHA content when using the most prevalent farming practices of grain corn feeding vs pasture-feeding. Thus, even for omnivores, obtaining DHA through the diet may be increasingly difficult in the current modern food climate. Paradoxically, in Asia, vegetarianism has been practiced for centuries without high incidence of cognitive impairment. No ill effects were reported in pregnancy outcomes of South Asian vegetarians vs North London omnivores [77] and Seventh Day Adventists residing in the Southwestern United States reported significantly less negative emotion compared with omnivores, despite reduced levels of DHA [78].

Due to the apparent discrepancy between animal studies showing clear cognitive impairment associated with reduced DHA in the brain and human data showing improved mental health in vegetarians, we sought to investigate whether other components commonly consumed in traditional vegetarian diets could enhance DHA content in the brain and the synthesis of DHA from vegetarian sources. In India 31% of the population are lacto-vegetarian or vegan [79]. Turmeric is a household staple in India, with reported average daily consumption ranging from 0.24 g/person/day to as high as 4g/person/day [80, 81]. Curcumin, which is a naturally polyphenolic compound found in turmeric has multifaceted medicinal properties and has been implicated in helping to treat several types of neurological disorders including Alzheimer’s disease [39, 82, 83], retinal diseases [84, 85], Parkinson’s disease [86, 87], stroke [88], brain injury [22, 41, 42] and psychiatric disorders [89–91]. We recently reported that curcumin supplementation promoted increased DHA content in the brain following TBI, and that this effect was associated with elevated levels of enzymes involved in DHA synthesis [22]. We therefore investigated whether curcumin enhances DHA synthesis from vegetarian precursors. Here we report that, when combined with dietary ALA, curcumin increases the DHA content in both liver and brain tissues. Furthermore, we found that the elevated DHA content was associated with elevated levels of the enzymes FADS2 and elongase 2, which are important for DHA synthesis.

Emerging evidence indicates that hepatic DHA synthesis from ALA increases the DHA supply to the brain, but the rate of DHA conversion from its precursors is low [28, 92]. This may be partially due to the fact that the plant-derived omega 6 and omega 3 fatty acids linoleic acid (18:2 n-6;LA) and ALA, respectively, compete for enzymes to catalyze the desaturation and elongation reactions in order to generate longer chain fatty acids. There are two stages involved in the process of DHA synthesis from ALA. The first stage includes a series of elongation by elongases such as Elov5 and desaturation by desaturases such as FADS1 (Δ5-desaturase) and FADS2 (Δ6-desaturase) ( ). This results in the conversion of ALA to eicosapentaenoic acid (C20:5 n-3; EPA). The second stage involves the conversion from EPA to docosapentaenoic acid (C22:5 n-3; DPA) and ultimately to DHA. In mammals, this process involves elongation (by elongases), desaturation (FADS2), and β-oxidation (by Acox1 and 17β-HSD4) [93]. In particular, the intermediate C22:5 n-3 is converted to C24:6 n-3, which is then retroconverted to C22:6 n-3 (DHA) [94, 95]. It has been reported that in order to achieve similar amounts of long chain omega 3 fatty acids in the brain on an ALA enriched, vs a preformed EPA + DHA enriched diet, ALA needed to be consumed at 33.5 times the amount [96]. The action of FADS2 and Elov2 are important control points (enzymatic reaction-limitation) during the synthesis of DHA. Excessive ALA consumption may inhibit the activity of enzymes involved in DHA synthesis. In particular FADS2 is subject to competitive inhibition between substrates. For example, administration of ALA to HepG2 cells results in increased accumulation of EPA, but not DHA, consistent with competitive inhibition of FADS2 by DPA [52]. We found that, when combined with the vegetarian precursor ALA, dietary curcumin increased levels of FADS2 and elongase 2 in both liver and brain tissues. Accordingly, our results showed that curcumin produced greater hepatic and central DHA increases compared to animals fed ALA alone. Thus, our data support that by increasing the level of these key enzymes curcumin may enhance the conversion of ALA to DHA, even when ALA levels are increased in the diet. Accordingly, our in vitro data suggest that the effects of curcumin to enhance DHA synthesis are dependent on the effective functioning of FASD2 enzyme, suggesting that curcumin effects are partially at the level of DHA synthesis.

We report that curcumin significantly increased the synthesis of DHA from DPA in cultured liver cells. These data strongly suggest that curcumin increases the hepatic synthesis of DHA from its precursors. Since the liver is the primary site for most of the DHA synthesis in the body, this raises the question as to whether some of the health effects of curcumin can be attributed to the synthesis of DHA. For example, deficient liver biosynthesis of DHA was linked to cognitive impairment in Alzheimer’s patients who showed reduced expression of enzymes involved in DHA synthesis [3]. We report that feeding animals a combination of curcumin and ALA elevated DHA content in both the liver and the brain. Furthermore, elevations in brain DHA were closely associated with the reduced anxiety-like behavior tested by EPM. These results are in agreement with previous studies describing an association between DHA dietary deficiency and anxiety-like behavior [2].

Herein we report that curcumin elevates levels of DHA in the brain, and that these effects required the presence of ALA in the diet. Curcumin has been reported to cross the blood brain barrier [97, 98], and to be neuroprotective [99][41, 100, 101]. It is known that DHA is an essential component of nerve cell membranes [102, 103], but the synthesis of DHA is very limited in the brain [29]. Sources of DHA for the brain include dietary sources such as fish and DHA synthesized by the liver from precursors such as ALA (C18:3n-3), DPA (C22:5n-3), EPA (C20:5n-3), and tetracosahexaenoic acid (C24:6n-3) [104–107]. Our current study provides new evidence indicating that curcumin increases levels of enzymes FADS2 and elongase 2, which are involved in DHA synthesis, in brain tissue. Additionally, we found that brain levels of DHA and DHA synthesis enzymes were enriched in animals fed curcumin and ALA together, but were unchanged when rats were fed the ALA-enriched diet without curcumin. Though the rate of synthesis is low, the brain seems to have the capacity to synthesis DHA from ALA [29]. Thus it is possible that curcumin elevates DHA in the brain, in part, through de novo synthesis in brain tissue. This possibility warrants further investigation, though liver synthesis seems the more likely contributor to increased brain pools of DHA, since curcumin is highly metabolized in the liver [108]. From our current dataset, we cannot exclude the possibility that observed elevations in brain DHA comes from the liver, since curcumin also promotes the DHA synthesis in the liver.

Curcumin has known antioxidant, anti-inflammatory and antiapoptotic properties (for review see [109]), thus we cannot exclude the possibility that elevated levels of DHA measured in brain and liver are the indirect result of reduced oxidative stress or anti-inflammatory properties of curcumin. For example, oxidative stress is inversely related to liver FASD2 and Δ5 desaturase activities and it has been hypothesized that reduction in plasma antioxidant activity may promote the direct inactivation or reduced expression of liver FASD2 [110]. Thus, the effect of curcumin on levels of FASD2 may be indirectly related to its antioxidant properties. During oxidative stress free radicals generate lipid degradation products, such as 4-HNE. We measured levels of 4-HNE in brain and liver tissues as a biomarker of oxidative stress. Surprisingly, curcumin alone did not reduce 4-HNE in brain or liver, suggesting that curcumin alone in the diet did not reduce lipid peroxidation under homeostatic conditions. In these terms, it is likely that the antioxidant action of curcumin may be more prevalent under challenging conditions such as brain injury. Treatment with ALA either alone or in combination with curcumin significantly reduced levels of 4-HNE. In brain tissue, the combined treatment with ALA and curcumin further reduced lipid peroxidation, whereas in liver it did not. Interestingly, ALA alone was associated with elevated DHA in the liver, but not in the brain. Therefore, if levels of DHA contributed to the reduced lipid peroxidation, we would expect the differences between the ALA group and the ALA + CUR groups to be greater in the brain compared with the liver, which is what the data show. Herein we report that curcumin + ALA elevates levels of enzymes related to DHA synthesis, elevates levels of DHA in brain and liver, as well as reduces n-6 precursors in the liver, suggesting that it is likely that curcumin increases the synthesis of DHA from the ALA precursor in vivo, further studies are warranted to elucidate whether affecting synthesis is the mechanism by which curcumin enhances DHA levels in the liver and brain.