Upregulation of BDNF and hippocampal functions by a hippocampal ligand of PPARα

behaviors in 5XFAD Ppar α -null and 5XFAD Ppar α - Δ Hippo mice, indicating an essential role of hippocampal PPAR α in Hex-mediated improvement in hippocampal functions. This is the first demonstration to our knowledge of protection of hippocampal functions by oral administration of a hippocampus-based drug, suggesting that Hex may be explored for therapeutic intervention in AD. oral administration of Hex significantly the level of PSD95 protein in the hippocampi of Hex-fed 5XFAD mice in comparison with vehicle-fed mice. To further characterize the role of Hex in the regulation of synaptic functions, we next investigated the expression of GLUR1 and NR2A, 2 proteins belonging to ionotropic glutamate receptor family that are long known to play important roles in postsynaptic calcium influx (20). We found that protein levels of both GluR1 and NR2A were significantly low in the hippocampi of vehicle-fed 5XFAD mice as compared with that in non-Tg mice C, H, and I). However, oral treatment of Hex markedly enhanced the levels of GluR1 and NR2A in the hippocampi of 5XFAD mice C, H, and I). Together, these results indicate that Hex may control hippocampal plasticity by regulating the hippocampal expression of some of the notable plasticity-associated molecules. Hex promotes hippocampal synaptic functions in 5XFAD mice . It has been reported that cognitive decline pos-itively correlates with reduced number of positive clusters for PSD95, an indicator of loss of actual synapses Therefore, we next explored a possible association of Hex-mediated upregulation of PSD95 with altered spine morphology. Therefore, we immunolabeled the hippocampal slices harvested from mice across all groups with MAP2, a neuronal marker, and PSD95. As expected, the number of puncta positive for MAP2 ionotropic glutamate receptors, including NMDA and AMPA receptors, is directly linked to the loss of learning and memory (41). Consistent with the increase in Ca 2+ influx, Hex treatment also improved spatial learning and memory and short-term memory in 5XFAD mice. On the other hand, we did not notice any drug-related side effect (e.g., hair loss, weight loss, untoward infection, etc.) in any of the mice used during the course of the study. These results suggest that oral Hex may have therapeutic importance for the protection of hippocampal plasticity and memory in AD. α α ligand–binding BDNF α flPPAR α Y464D-PPAR α BDNF upregulation, role of Y464 of PPAR α in neurotrophic


Introduction
Alzheimer's disease (AD) is an irreversible and a progressive form of dementia that slowly destroys cognitive functions; it is severe enough to interfere with activities of daily living. According to CDC, currently AD is officially ranked as the sixth leading cause of death in the United States (1). Accumulating evidences link AD pathology with reduced BDNF levels in the serum (2) and in the cognition-related structures, such the as hippocampus and frontal cortex (3). BDNF is a prominent neurotrophin that regulates many of the hippocampus-based biological processes that include maintenance and survival of hippocampal neurons (4), promoting hippocampal dendritic spine density and morphology (5), and enhancing hippocampal neurogenesis (6). Additionally, using BDNF-knockout mouse lines, researchers have implicated the involvement of BDNF in long-term potentiation (7,8). Considering its essential role in providing trophic support to degenerating neurons and promoting postsynaptic functions, BDNF has, therefore, gained an enormous attention as a promising therapeutic target in countering AD pathology. However, current BDNF-based therapeutics are not that effective in delivering desirable relief to patients with AD. Therefore, enhancing the production of BDNF in vivo in the hippocampus using safer and effective approaches is presently an important area of research.
Recently, we found that hexadecanamide (Hex) is present in vivo in hippocampal nuclei of normal mice as an endogenous ligand of PPARα (9). Here, we demonstrated that Hex upregulated BDNF and stimulated synaptic functions in cultured hippocampal neurons and in vivo in the hippocampi of 5XFAD mice. In addition, we also noticed an improvement in hippocampus-based cognitive behaviors following oral administration of Hex in 5XFAD mice. While investigating the underlined mechanism, we found that Hex rendered these neuroprotective effects through hippocampal PPARα. These results highlight the protection of spatial learning and memory by a hippocampal drug in an animal model of AD.
Discovery strategies commonly focus on the identification of chemical libraries or natural products, but the modulation of endogenous ligands offers a much better therapeutic strategy due to their low adverse potential. Recently, we found that hexadecanamide (Hex) is present in hippocampal nuclei of normal mice as an endogenous ligand of PPARα. This study underlines the importance of Hex in inducing the expression of brain-derived neurotrophic factor (BDNF) from hippocampal neurons via PPARα. The level of Hex was lower in the hippocampi of 5XFAD mice as compared with that in non-Tg mice. Oral administration of Hex increased the level of this molecule in the hippocampus to stimulate BDNF and its downstream plasticity-associated molecules, promote synaptic functions in the hippocampus, and improve memory and learning in 5XFAD mice. However, oral Hex remained unable to stimulate hippocampal plasticity and improve cognitive behaviors in 5XFAD Pparα-null and 5XFAD Pparα-ΔHippo mice, indicating an essential role of hippocampal PPARα in Hex-mediated improvement in hippocampal functions. This is the first demonstration to our knowledge of protection of hippocampal functions by oral administration of a hippocampusbased drug, suggesting that Hex may be explored for therapeutic intervention in AD. Primary hippocampal neurons derived from E18 C57BL6 mice pups were treated at 14 days in vitro (DIV) with increasing doses of Hex (μM) for 5 hours, followed by mRNA expression analyses of different members of the neurotrophin family (Bdnf, NT3, and NT4) along with their receptors (TrkB and P75 NTR ) using semiquantitative RT-PCR (A) and quantitative real-time PCR (B). Expression of GAPDH mRNA was used as loading control. Results are shown as mean ± SD, and 1-way ANOVA [Bdnf mRNA, F (2,6) = 17.990, P = 0.003; NT3 mRNA, F (2,6) = 18.058; NT4 mRNA, F (2,6) = 3.9702, P = 0.080; TrkB mRNA, F (2,6) = 27.393, P < 0.001; P75 NTR mRNA, F (2,6) = 3.6634; P = 0.091] followed by Bonferroni's multiple comparisons test, was used to assess significance of the mean; *P < 0.05, **P < 0.01 vs. control. Following dose-dependent treatment with Hex (μM) for 12 hours, the protein expression of BDNF (C), NT3 (F), and TrkB (I) was investigated in the primary hippocampal neurons by immunoblot analysis (see complete unedited blots in the supplemental material). Relative densities of BDNF (D), NT3 (G), and TrkB (J) protein expressions compared with β-actin were calculated by ImageJ. Results are shown as mean ± SD and 1-way ANOVA [BDNF protein, F (2,6) = 8.9312, P = 0.016; NT3 protein, F (2,6) = 52.019, P < 0.001; TrkB protein, F (2,6) = 8.7881, P = 0.02] followed by Bonferroni's multiple comparisons test was used to assess significance of the mean; *P < 0.05, **P < 0.01 vs. control. BDNF and NT3 protein levels were also investigated by immunostaining Hex-treated primary hippocampal neurons with neuronal marker MAP2 (green) and BDNF (red) (E) or MAP2 (green) and NT3 (red) (H). Scale bars: 20 μm.
proteins and signaling molecules present in the niche of postsynaptic density (18,19). Hence, we analyzed whether Hex treatment could enhance the level of PSD95 in the hippocampi of 5XFAD mice. As evident from our immunoblot analyses ( Figure 2C) and corresponding densitometric analyses ( Figure 2G), oral administration of Hex significantly increased the level of PSD95 protein in the hippocampi of Hex-fed 5XFAD mice in comparison with vehicle-fed mice. To further characterize the role of Hex in the regulation of synaptic functions, we next investigated the expression of GLUR1 and NR2A, 2 proteins belonging to ionotropic glutamate receptor family that are long known to play important roles in postsynaptic calcium influx (20). We found that protein levels of both GluR1 and NR2A were significantly low in the hippocampi of vehicle-fed 5XFAD mice as compared with that in non-Tg mice (Figure 2, C, H, and I). However, oral treatment of Hex markedly enhanced the levels of GluR1 and NR2A in the hippocampi of 5XFAD mice (Figure 2, C, H, and I). Together, these results indicate that Hex may control hippocampal plasticity by regulating the hippocampal expression of some of the notable plasticity-associated molecules.
Hex promotes hippocampal synaptic functions in 5XFAD mice. It has been reported that cognitive decline positively correlates with reduced number of positive clusters for PSD95, an indicator of loss of actual synapses (21). Therefore, we next explored a possible association of Hex-mediated upregulation of PSD95 with altered spine morphology. Therefore, we immunolabeled the hippocampal slices harvested from mice across all groups with MAP2, a neuronal marker, and PSD95. As expected, the number of puncta positive for MAP2 and PSD95 was markedly decreased in 5XFAD mice compared with that in non-Tg mice ( Figure 3, A and B). However, the observed reduction in puncta positive for MAP2 and PSD95 in hippocampi was significantly rescued in 5XFAD mice following Hex treatment ( Figure 3, A and B). AMPA-mediated and NMDAR-mediated Ca 2+ influx have been implicated in long-lasting forms of synaptic plasticity and higher cognitive functions (22,23). Therefore, we also analyzed the effect of Hex on the ionotropic calcium influx through AMPA and NMDA receptors in hippocampal slices of 5XFAD mice. Consistent with the increased hippocampal expression of GluR1 and NR2A proteins (Figure 2, C, H, and I), oral administration of Hex upregulated AMPA-( Figure 3C), and NMDA-dependent ( Figure 3D), calcium influx in hippocampal slices of 5XFAD mice as compared with that in vehicle-fed 5XFAD mice. In summary, Hex-mediated protective effects on postsynaptic marker clusters and calcium currents in the hippocampus suggest that Hex may ameliorate AD-associated cognitive defects by promoting these synaptic morphological and functional improvements.
Hex-mediated upregulation of hippocampal BDNF is dependent on PPARα. Next, we investigated mechanisms by which Hex upregulated BDNF in hippocampal neurons. BDNF is a well-established downstream target of cAMP response element-binding protein (CREB) (24), a transcription factor that plays an important role in promoting synaptic activity. Previously, we reported that PPARα directly binds to CREB promoter to promote the expression of CREB and CREB-dependent neurotrophic factors (25,26). Therefore, we analyzed whether Hex required PPARα to stimulate the expression of BDNF in the hippocampal neurons. Interestingly, Hex stimulated the expression of Bdnf mRNA ( Figure 4A) and protein ( Figure 4, B and C) in WT, but not Pparα-null, hippocampal neurons. To further confirm a direct role for PPARα in the hippocampal BDNF upregulation, we overexpressed the lentiviral construct containing full-length PPARα (lenti-flPPARα) in Pparα-null hippocampal neurons, followed by stimulation with Hex and assessment of Bdnf mRNA ( Figure 4D) and protein ( Figure 4, E and F). Interestingly, transduction of lenti-flPPARα enhanced both mRNA and protein levels of BDNF in Hex-treated Pparα-null hippocampal neurons. Since HEX binds to Y464 of PPARα (9), we also transduced Pparα-null hippocampal neurons with mutated lenti-Y464D-PPARα. In contrast to lenti-flPPARα-transduced neurons, HEX remained unable to upregulate BDNF mRNA and protein in lenti-Y464D-PPARα-transduced Pparα-null hippocampal neurons (Figure 4, E and F). Taken together, these results suggest that HEX requires PPARα to upregulate BDNF in hippocampal neurons.
To further understand the functional significance of Hex-mediated upregulation of BDNF via PPARα, we examined the involvement of PPARα in Hex-mediated protection of hippocampal properties using 5XFAD and 5XFAD mice with global deletion of PPARα. 5XFAD Pparα-null mice were generated to study the role of PPARα in AD-related pathologies in mice (27,28). As expected, following 1 month of Hex (5 mg/kg/d) treatment, we observed a significant increase in BDNF in the hippocampi of 5XFAD, but not that in 5XFAD Pparα-null , mice ( Figure 5, A and B). The involvement of PPARα in Hex-mediated BDNF protein upregulation was again investigated by double labeling hippocampal sections with BDNF and MAP2 antibodies ( Figure 5, C and D, and Supplemental Figure 2A). Hexfed 5XFAD mice showed a significant increase in BDNF in the hippocampus as compared with that Figure 2. Hex upregulates BDNF and other hippocampal plasticity-associated proteins in the hippocampi of 5XFAD mice. 5XFAD mice (n = 6/group; 6-7 months old) were treated orally with Hex (5 mg/kg/d) or vehicle (0.1% methyl cellulose) for 1 month. Untreated non-Tg (NTG) mice (n = 6) were used as control. Following 1 month of Hex treatment, the mRNA expression of several plasticity-associated genes was analyzed by real-time PCR, followed by gene array analysis. GAPDH was used as an endogenous control. (A) Heatmap showing relative expression of differentially regulated plasticity genes in hippocampi of NTG or Hex-fed 5XFAD mice compared with that of vehicle-fed 5XFAD mice. (B) Venn diagram summarizing the numbers of differentially regulated plasticity genes. Relative expression greater than 2 was considered statistically significant. (C) Similarly, following 1 month of Hex treatment, protein levels in hippocampal homogenates of selected plasticity-associated molecules (BDNF, PSD95, GluR1, and NR2A) were analyzed by immunoblot analysis. β-Actin was used as a loading control. Uncropped Western blot images are shown in Supplemental Figure 6. Relative densities of BDNF (D), PSD95 (G), GLUR1 (H), and NR2A (I) immunoblots compared with that of β-actin were calculated by ImageJ. Results are shown as mean ± SEM. One-way ANOVA [BDNF protein, F (2,15) = 6.5000, P = 0.009; PSD95 protein, F (2,15) = 23.977, P < 0.001; GLUR1 protein, F (2,15) = 74.063, P < 0.001; in vehicle-fed 5XFAD mice ( Figure 5, C and D, and Supplemental Figure 2A). On the other hand, while analyzing BDNF expression in 5XFAD Pparα-null mice, we did not find any significant difference in BDNF between vehicle-fed 5XFAD Pparα-null mice and Hex-fed 5XFAD Pparα-null mice ( Figure 5, C and D, and Supplemental Figure 2A). Together, these results suggest that PPARα plays an essential role in Hex-mediated induction of BDNF expression in the hippocampi of 5XFAD mice.
Hex-mediated improved hippocampal synaptic functions is dependent on PPARα. As shown above, following Hex treatment, we noticed a significant upregulation in PSD95 in the hippocampi of 5XFAD mice (Figure 5, A and B). However, Hex did not have any significant effect on hippocampal PSD95 expression in 5XFAD Pparα-null mice when compared with vehicle-fed 5XFAD mice ( Figure 5, A and B). Consistently, as evident from increased PSD95-and MAP2-positive puncta, we also observed an increase in the colocalization of postsynaptic PSD95 and neuronal marker MAP2 in the hippocampi of Hex-fed 5XFAD mice as compared with that in vehicle-fed 5XFAD mice ( Figure 5, C and E, and Supplemental Figure 2B). However, the effect of Hex on PSD95 appeared specific to PPARα, because we did not detect any significant differences in the number of PSD95-and MAP2-positive puncta in the hippocampus between vehicle-fed and Hex-fed 5XFAD Pparα-null mice ( Figure 5, C and E, and Supplemental Figure 2B).
Since treatment with Hex, a hippocampal ligand of PPARα (9), elicited both AMPA-dependent and NMDA-dependent postsynaptic calcium currents in the hippocampi of 5XFAD mice (Figure 3, C and D), we next investigated whether global knockdown or hippocampus-specific deletion of PPARα interfered with Hex-induced postsynaptic calcium currents in 5XFAD mice. Therefore, using the Cre-lox mechanism, we first generated 5XFAD Pparα-ΔHippo mice, 5XFAD mice with deletion of PPARα in hippocampal neurons (Supplemental Figure 3). Next, we analyzed the effect of Hex treatment on the ionotropic calcium influx through NMDA and AMPA receptors in the hippocampal slices of 5XFAD mice with functional PPARα, 5XFAD Pparα-null mice with global knockdown of PPARα, and 5XFAD Pparα-ΔHippo mice with hippocampus-specific deletion of PPARα. Consistent with the increased hippocampal expression of BDNF and PSD95 proteins, Hex feeding upregulated AMPA-dependent ( Figure 6A), and NMDA-dependent ( Figure 6B), calcium influx, as measured in hippocampal slices of 5XFAD mice but neither 5XFAD Pparα-null nor 5XFAD Pparα-ΔHippo mice. Together, these results demonstrate that Hex requires hippocampal PPARα in controlling the expression of plasticity-associated molecules and their function in vivo in hippocampus.
Hex protects hippocampus-based spatial and recognition memories via PPARα. Finally, we investigated the effect of Hex at the therapeutic level. Therefore, we analyzed some of the hippocampus-dependent behaviors in the 5XFAD, 5XFAD Pparα-null , and 5XFAD Pparα-ΔHippo mice following Hex treatment. Hippocampus-based spatial learning and context-dependent behavior can be reliably monitored in the Barnes maze test and T-maze test, respectively (25,27). As noted in our previous reports (26,27,29), 5XFAD mice displayed decreased spatial behaviors indicated by increased latency ( Figure 6D) and errors ( Figure 6E) as compared with age-matched non-Tg mice. However, Hex feeding significantly improved latency ( Figure 6D) and decreased errors (Figure 6E) in 5XFAD mice. In contrast, Hex treatment remained unable to improve spatial learning in both 5XFAD Pparα-null and 5XFAD Pparα-ΔHippo mice, indicating an essential role for hippocampal PPARα in Hex-mediated improvement in hippocampus-dependent spatial memory ( Figure 6, C and D). Consistently, our T-maze test also exhibited significant improvement in the performance of 5XFAD, as shown by increase in the number of positive turns ( Figure 6F) and reduction of errors ( Figure 6G), whereas 5XFAD Pparα-null mice and 5XFAD Pparα-ΔHippo mice did not display any improvement in T maze analyses (Figure 6, F and G), following Hex treatment, indicating a pivotal role of hippocampal PPARα in Hex-mediated improvement in spatial and contextual in 5XFAD mice. Furthermore, hippocampus is also critical for the processing of memory required for object recognition (30,31). Therefore, we also investigated the effect of Hex on memory associated with recognition of an object by analyzing the performance of mice in the novel object recognition test (Supplemental Figure 4A). Interestingly, vehicle-fed 5XFAD mice were clearly impaired in their ability to distinguish the novel object, whereas 5XFAD mice treated with Hex behaved very similar to the non-Tg mice with increased preferences for the novel object (Supplemental Figure 4B). In contrast, Hex treatment was unable to NR2A protein, F (2,15) = 19.624, P < 0.001], followed by Bonferroni's multiple comparisons test was used to assess significance of the mean; *P < 0.05 vs. vehicle-fed 5XFAD; **P < 0.01, ***P < 0.001 vs. vehicle-fed 5XFAD. Hippocampal sections were also double labeled for MAP2 (green) and BDNF (red) (E). Scale bars: 50 μm. (F) MFI of hippocampal BDNF was calculated using ImageJ. For quantification, 2 sections per mice (n = 6/group) were used. Results are shown as mean ± SEM. One-way ANOVA [BDNF MFI: F (2,33) = 115.77, P < 0.001] followed by Bonferroni's multiple comparisons test was used to assess significance of the mean; **P < 0.01 vs. vehicle-fed 5XFAD. Figure 3. Hex promotes synaptic functions in the hippocampi of 5XFAD mice. (A) 5XFAD mice (n = 6/group; 6-7 months old) were treated orally with Hex (5 mg/kg/d) or vehicle (0.1% methyl cellulose) for 1 month. Untreated non-Tg (NTG) mice (n = 6) were used as control. Following 1 month of treatment, PSD95 protein levels were investigated by immunostaining hippocampal tissue harvested from hippocampi of NTG and vehicle fed-and Hex-fed 5XFAD mice with antibodies against neuronal marker MAP2 (green) and PSD95 (red). Scale bars: 50 μm. (B) Colocalization of PSD95 with MAP2 was analyzed by quantifying PSD95 and MAP2 immunoreactive puncta using ImageJ. For quantification, 2 sections per mice (n = 6/group) were used. Results are shown as mean ± SEM. One-way ANOVA [PSD95 puncta: F (2,33) = 39.712, P < 0.001], followed by Bonferroni's multiple comparisons test, was used to assess significance of the mean; **P < 0.01 vs. vehicle-fed 5XFAD. (C) AMPA-dependent and (D) NMDA-dependent calcium currents measured in the hippocampal slices of NTG, vehicle-fed, and Hex-fed 5XFAD mice. The arrow indicates the application of AMPA and NMDA in the assay. To nullify the secondary involvement of AMPA receptor in NMDA-dependent calcium currents, hippocampal slices were treated with NMDA together with NASPM (Ca 2+ -permeable AMPA antagonist), followed by the recording of calcium influx. Similarly, AMPA-dependent calcium influx was measured in the presence of N20C (noncompetitive NMDA open-channel blocker). Calcium influx was monitored for 300 repeats in a PerkinElmer VICTOR X2 fluorimeter. Results represent the mean of 3 independent experiments.
improve the ability to distinguish the novel object in both 5XFAD Pparα-null mice and 5XFAD Pparα-ΔHippo mice (Supplemental Figure 4B). Together, these observations suggest that Hex requires hippocampal PPARα to improve the memory in 5XFAD mice. Because the decreased latency in either Barnes maze or T-maze test could be confounded with the increased locomotion of animals, we also monitored the locomotor activity of these animals (Supplemental Figure 5A). We did not observe any significant difference in total distance moved (Supplemental Figure 5B) and velocity (Supplemental Figure 5C) across all different groups of animals, nullifying the possibility of interference by increased locomotion in the hippocampus-dependent behaviors. Collectively, these results demonstrate that Hex upregulates BDNF and its downstream signaling pathways and improves hippocampus-based cognitive behaviors in a mouse model of AD via hippocampal PPARα.

Discussion
AD is the most common form of dementia, causing a progressive decline of cognitive functions (32). A growing body of evidences suggests that AD is associated with multimodal pathologies triggered by concurrent occurrence of various fundamental changes in the cellular signaling pathways (33). Among these AD-associated pathologies, one deleterious effect that has attracted much attention in AD research is the downregulation of hippocampus-based neuroprotective molecules, especially BDNF (34). BDNF is the most widely distributed neurotrophin in the CNS that plays a pivotal role in regulating synaptic plasticity and neuronal survival (4,5,35). It has been reported that BDNF polymorphisms and reduced BDNF expression in human brains are closely associated with the pathogenesis of AD (2,3). Preclinical data are also available in the literature to provide valuable insight about the therapeutic potential of BDNF in the treatment for AD (36,37). However, there has been difficulty in translating BDNF-based therapy to the clinic. One possible explanation for this is the inability of BDNF in its free form to penetrate the bloodbrain barrier (38,39). Therefore, it is necessary to find safe drugs that can stimulate the endogenous BDNF to its therapeutic levels, especially in the hippocampus (40).
Although Hex or palmitamide is a primary fatty acid amide derived from palmitic acid, the most common saturated fatty acid found in animals, plants, and microorganisms, its biological effects are poorly understood. In this study, we demonstrate for the first time to our knowledge that Hex is capable of upregulating neurotrophic factors in hippocampal neurons. In cultured mouse hippocampal neurons, Hex alone induced the expression of BDNF and NT3. This upregulation was specific, as Hex had no effect on NT4. While Hex induced the expression of TrkB, it remained unable to increase the level of p75 NTR , again exhibiting the specificity. Because the loss of these neurotrophic factors has been implicated in the pathogenesis of various neurodegenerative diseases, our results provide a potentially important mechanism whereby Hex may ameliorate or delay neurodegeneration in AD.
While many drugs show therapeutic effects in cell culture models, very few exhibit efficacy in vivo in the brain. It is therefore remarkable that after oral feeding Hex entered into the hippocampus and exhibited a neurotrophic effect in the 5XFAD mouse model of AD. First, oral administration of Hex increased the level of BDNF and different plasticity-related molecules, including NMDA-and AMPA-regulated ionotropic receptors in the hippocampi of 5XFAD mice. Second, oral Hex upregulated Ca 2+ influx in the hippocampi of 5XFAD mice through NMDA and AMPA receptors. Third, impaired Ca 2+ influx through Bonferroni's multiple comparisons test was applied to assess the significance of the mean; **P < 0.01 vs. control, ns P > 0.05 vs. control. (B) Cells were also treated with Hex for 12 hours and BDNF protein level was investigated by immunostaining. Scale bars: 20 μm. (C) MFI of hippocampal BDNF. Statistical analyses were performed using 2-way ANOVA considering genotype [F (1,32) = 44.55, P < 0.001] and treatment [F (1,32) = 19.53, P < 0.001] as 2 independent variables. Interaction statistics between 2 independent variables was calculated as well [F (1,32) = 23.54, P < 0.001]. Bonferroni's multiple comparisons test was applied to assess the significance of the mean; ***P < 0.001 vs. control, ns P > 0.05 vs. control. (D) Pparα-null hippocampal neurons were transduced with either empty lentiviral vector (GFP) or with the lentiviral vector containing flPPARα or Y464DPPARα for 48 hours followed by stimulation with Hex. After 5 hours, cells were analyzed for Bdnf mRNA. Results are mean ± SD of 3 independent experiments. Statistical analyses of Bdnf mRNA expression analyses between groups were performed using 2-way ANOVA considering lentiviral treatment [F (2,12) = 9.318, P = 0.004] and Hex treatment [F (1,12) = 11.71, P = 0.005] as 2 independent variables. Interaction statistics between 2 independent variables was calculated [F (2,12) Figure 6. (B) Relative density of BDNF and PSD95 protein expressions compared with β-actin was calculated by ImageJ. Results are shown as mean ± SEM. One-way ANOVA followed by Bonferroni's multiple comparisons test was used to assess the significance of the mean; **P < 0.01 vs. vehicle-fed 5XFAD, ns P > 0.05 vs. vehicle-fed 5XFAD. (C) Hippocampal sections were double labeled with either BDNF (red) plus MAP2 (green) or PSD95 (red) plus MAP2 (green). Scale bar: 50 μm. Raw images are shown in Supplemental Figure 6. (D) MFI of hippocampal BDNF was quantified in 2 sections of each of 6 mice per group. One-way ANOVA [BDNF MFI: F (4,55) = 114.28, P < 0.001], followed by Bonferroni's multiple comparisons test was used; **P < 0.01 vs. vehicle-fed 5XFAD, ns P > 0.05 vs. vehicle-fed 5XFAD. (E) Colocalization of PSD95 with MAP2 was analyzed by quantifying PSD95 and MAP2 immunoreactive puncta using ImageJ. For quantification, 2 sections per mice (n = 6 per group) was used. Results are shown as mean ± SEM. One-way ANOVA [PSD95 puncta: F (4,55) = 52.569, P < 0.001], followed by Bonferroni's multiple comparisons test was used to assess the significance of the mean, **P < 0.01 vs. vehicle-fed 5XFAD, ns P > 0.05 vs. vehicle-fed 5XFAD. Figure 6. Hex promotes calcium influx and ameliorates cognitive deficits in 5XFAD mice via hippocampal PPARα. 5XFAD, 5XFAD Pparα-null , and 5XFAD Pparα-ΔHippo mice (n = 6/group; 6-7 months old) were orally treated with Hex (5 mg/kg body weight) or vehicle (0.1% methyl cellulose) for 30 days. Age-matched non-Tg (NTG) mice without any treatment (n = 6) were used as controls. Following treatment, AMPA-(A) and NMDA-dependent (B) calcium currents were measured in the ionotropic glutamate receptors, including NMDA and AMPA receptors, is directly linked to the loss of learning and memory (41). Consistent with the increase in Ca 2+ influx, Hex treatment also improved spatial learning and memory and short-term memory in 5XFAD mice. On the other hand, we did not notice any drug-related side effect (e.g., hair loss, weight loss, untoward infection, etc.) in any of the mice used during the course of the study. These results suggest that oral Hex may have therapeutic importance for the protection of hippocampal plasticity and memory in AD.
PPARα is a transcription factor that regulates fatty acid metabolism. Although liver, being the major fatty acid-metabolizing organ, is very rich in PPARα, we have seen that PPARα is constitutively expressed in hippocampal neurons (9,(25)(26)(27)42). Interestingly, we found the presence of Hex in the nuclei of hippocampal neurons as an endogenous ligand of PPARα (9). A ligand-binding triad of S280, Y314, and Y464 is critical for the interaction of PPARα with endogenous ligands (9) and other ligands (26,27,29). We have delineated that Hex is mainly bound to Y464 of the PPARα ligand-binding domain (9). Consistently, here, we have shown that Hex is unable to upregulate BDNF in the absence of PPARα and that lentiviral overexpression of flPPARα, but not mutated Y464D-PPARα, restores Hex-mediated BDNF upregulation, highlighting an important role of Y464 of PPARα in neurotrophic function of Hex. Accordingly, Hex treatment also failed to upregulate hippocampal BDNF, stimulate hippocampal plasticity, and improve any of the hippocampus-based memories in 5XFAD mice with either whole-body PPARα knockdown or hippocampus-specific PPARα knockdown, indicating an essential role of hippocampal PPARα in rendering Hex-mediated neuroprotection against AD-associated pathologies.
Currently, there is no effective therapy for halting the progression of AD. Use of memantine and different antagonists of cholinesterase, such as Aricept, Exelon, Razadyne, Cognex, etc., has been the standard treatment for AD (43). However, they are often associated with a number of side effects and disappointing results. On the other hand, there are a number of advantages of Hex over these proposed anti-AD therapies. First, in contrast to available AD therapies, Hex is physiological and present in the hippocampus. Second, Hex is very economical. Third, being the simple amide of the most common saturated fatty acid, Hex is fairly nontoxic. It could be converted into palmitic acid by FAAH to be metabolized completely by mitochondrial β-oxidation. It is interesting because inhibitors of FAAH have been reported to support hippocampal plasticity and protect memory (13). Therefore, it is possible that FAAH antagonists help to stabilize fatty acid amides such as Hex in the hippocampus to ultimately protect/stimulate memory and learning via PPARα.
In summary, we have demonstrated that Hex increases hippocampal BDNF, stimulates hippocampal plasticity, and improves cognitive functions in a mouse model of AD via hippocampal PPARα. These results highlight a potentially novel neurotrophic and neuroprotective role of Hex and suggest that this hippocampal endogenous molecule may be explored for therapeutic intervention in AD.

Methods
For cell culture, semiquantitative RT-PCR, real-time PCR, immunoblotting analysis, immunofluorescence analysis, and behavioral analysis, an extended section is provided in Supplemental Methods.
Reagents and antibodies. Antibodies, their applications, sources, and dilutions are listed in Supplemental Table  1. Cell culture materials (DMEMF/12, neurobasal, phenol red-free neurobasal, B27, L-glutamine, antibiotic/ antimycotic) were purchased from Life Technologies. Hex (A5376) was purchased from MilliporeSigma. All molecular biology-grade chemicals were obtained from either MilliporeSigma or Bio-Rad. Alexa Fluor secondary antibodies used for immunofluorescence analyses were obtained from Jackson ImmunoResearch, and IR-Dye-labeled secondary antibodies used for immunoblotting analyses were from Li-Cor Biosciences.
hippocampal slices of NTG, vehicle-fed or Hex-fed 5XFAD mice, vehicle-fed or Hex-fed 5XFAD Pparα-null mice, and vehicle-fed or Hex-fed 5XFAD Pparα-ΔHippo mice. Arrow indicates the application of AMPA and NMDA into the assay. Results represent 3 independent experiments. Following Hex treatment, hippocampus-dependent spatial behavior of mice across all groups was also analyzed using Barnes maze (BM). (C) Representative track plots summarizing the overall activity of mice on the apparatus recorded with a Noldus camera and visualized by Ethovision XT software. (D) Latency and (E) number of errors made by NTG, vehicle-fed or Hex-fed 5XFAD mice, vehicle-fed or Hex-fed 5XFAD Pparα-null mice, and vehicle-fed or Hex-fed 5XFAD Pparα-ΔHippo mice. Results are shown as mean ± SEM. One-way ANOVA [BM latency: F (6,35) = 23.28, P < 0.0001 and BM errors: F (6,35) = 16.002, P < 0.001], followed by Bonferroni's multiple comparisons test, was used to assess the significance of the mean; ***P < 0.001 vs. vehicle-fed 5XFAD, ns P > 0.05 vs. vehicle-fed 5XFAD. Context-dependent hippocampal behavior was analyzed by T-maze test. (F) Number of positive turns and (G) number of errors of NTG, control and Hex-treated 5XFAD, 5XFAD Pparα-null and 5XFAD Pparα-ΔHippo mice on an appetitive T maze conditioning task were manually recorded. Results are shown as mean ± SEM. One-way ANOVA [TM positive turns: F (6,35) = 5.361, P = 0.0005 and TM errors: F (6,35) = 5.361, P = 0.0005], followed by Bonferroni's multiple comparisons test, was used to assess the significance of the mean, *P < 0.05 vs. vehicle-fed 5XFAD, **P < 0.01 vs. vehicle-fed 5XFAD, ns P > 0.05 vs. vehicle-fed 5XFAD.
Animals. C57BL/6J mice, Pparα-null mice, and 5XFAD mice (44) were obtained from The Jackson Laboratory. Unless otherwise indicated, Pparα-null mice (45) were maintained as homozygous on a C57BL/6J background. 5XFAD Pparα-null mice, developed earlier in-house (42), were maintained Tg for the 5XFAD mutations and homozygous for the Pparα-null allele through genotyping using PCR on genomic DNA isolated from tail biopsies and detected by primers listed in Supplemental Table 2. Pparα ΔHippo mice that harbor conditional Pparα deletion in the hippocampal neuronal cells were generated by breeding Pparα flox mice (46) with B6.Cg-Tg (Camk2a-Cre) T29-1Stl/J mice expressing Cre recombinase under the guidance of the calcium/calmodulin-dependent protein kinase II α (Camk2a) promoter (obtained from The Jackson Laboratory). Genotyping of the Pparα flox locus and Camk2a-Cre Tg (Supplemental Figure 3) was performed using PCR on DNA from tail biopsies and detected by primers listed in Supplemental Table 2. Next, Pparα ΔHippo mice were crossed with 5XFAD mice to generate pups heterozygous for both the Pparα ΔHippo allele and the 5XFAD Tgs. These mice were then backcrossed with homozygous Pparα ΔHippo mice to generate approximately 25% 5XFAD Pparα-ΔHippo mice (Supplemental Figure 3). 5XFAD, 5XFAD Pparα-null , and 5XFAD Pparα-ΔHippo mice were aged 6 to 6.5 months at time of treatment and allowed to survive for another 4-6 weeks before they were sacrificed, and their brains were harvested for further analyses.
Organotypic calcium influx assay. Calcium influx measurement in the mouse hippocampal slices was performed as described previously (26,27). Briefly, 5XFAD mice, 5XFAD Pparα-null mice, 5XFAD Pparα-ΔHippo mice and age-matched non-Tg mice, were anesthetized, rapidly perfused with ice cold sterile PBS, and the whole brain was carefully removed from the cranium. Dorsoventral slices of the hippocampus were made at a thickness of 100 μm using an adult mouse brain slicer matrix with 1.0-mm coronal section slice intervals. The slices were placed in the glass tray filled with cutting solution (24.56 g sucrose, 0.9008 g dextrose, 0.0881 g ascorbate, 0.1650 g sodium pyruvate, and 0.2703 g myo-inositol in 500 mL distilled water) and continuously bubbled with 5% CO 2 and 95% O 2 gas mixture. The glass tray was kept ice cold during the slicing period. Slices were then carefully transferred into Fluo-4 dye-containing reaction buffer. The reaction buffer was made before the making of brain slices using 10 mL artificial CSF (119 mM NaCl, 26.2 mM NaHCO 3, 2.5 mM KCl, 1 mM NaH 2 PO 4, 1.3 mM MgCl 2, 10 mM glucose, bubbled with 5% CO 2 and 95% O 2 followed by the addition of 2.5 mM CaCl 2 ) added to 1 bottle of Fluo-4 dye (catalog F10471 , ThermoFisher) and 250 mM probenecid. Before transferring slices, a flat-bottom 96-well plate (BD Falcon, catalog 323519) was loaded with 50 μL reaction buffer per well, covered with aluminum foil, and kept in a dark place. One individual slice was placed in each well loaded with reaction buffer, and the plate was rewrapped with aluminum foil and kept at 37°C for 20 minutes. After that, fluorescence excitation and emission spectra were recorded in a Perkin-Elmer Victor X2 Luminescence spectrometer in the presence of NMDA (50 μM) and AMPA (50 μM). The recording was performed with 300 repeats at 0.1-ms intervals.
qPCR-based microarray analyses. qPCR-based microarray using total RNA isolated from hippocampal tissues of non-Tg, vehicle-fed, and Hex-fed 5XFAD mice was performed as described previously (9,47). Briefly, 5XFAD mice were either treated with vehicle (0.1% methyl cellulose) or with Hex (5 mg/kg/d) for 1 month orally. Age-matched non-Tg mice without any treatment were used as control. Following 1 month of treatment, mice across all groups were anesthetized, rapidly perfused with ice-cold sterile PBS, and decapitated. The whole brain was carefully removed from the cranium, and the hippocampus was harvested. Total RNA was isolated from hippocampal tissue using the QIAGEN RNA isolation kit following the manufacturer's protocol. Next, cDNA was synthesized from isolated RNA as described previously (25,27). Synthesized cDNA was then amplified using SYBR green technology in the ABI Prism 7700 sequence detection system and PCR primer sets of key genes listed in Supplemental Table 3. The resulting Ct value was normalized with the housekeeping gene GAPDH and analyzed using the matrix visualization and analysis platform Morpheus (https://software.broadinstitute.org/morpheus/). The expression of mRNAs with fold change >2 or <-2 was defined as differentially expressed genes.
GC-MS analysis. The endogenous levels of Hex in the hippocampi of harvested brains from mice across all groups was performed using GC-MS as described previously (9,26,27). Briefly, 5XFAD mice were either treated with Hex (5 mg/kg/d) or vehicle (0.1% methyl cellulose). Following 1 month of treatment, mice were anesthetized, rapidly perfused with ice-cold sterile PBS, and decapitated. The whole brain was carefully removed from the cranium, and the hippocampus was harvested. Isolated hippocampus was homogenized in ice-cold nondetergent hypotonic buffer (10 mM HEPES [pH 7.9], 1.5 mM MgCl 2 , 10 mM KCl, 100 mM DTT, protease and phosphatase inhibitor cocktail). After 10 minutes of additional incubation in the hypotonic buffer, the hippocampal homogenate was centrifuged at 8000 g at 4°C for 10 minutes.
Next, the pellet was homogenized in ice-cold extraction buffer (10 mM HEPES [pH 7.9], 1.5 mM MgCl 2 , 0.21 M NaCl, 0.2 mM EDTA, 25% [v/v] glycerol, 100 mM DTT, protease and phosphatase inhibitor cocktail), placed on a rotating shaker at 4°C for 1 hour, and then centrifuged at 18,000 g for 10 minutes. The supernatant was next transferred to a methanol/chloroform/water (4:3:1) mixture and then centrifuged at 18,000 g for 90 seconds. The organic phase was collected, evaporated in the speedvac (Centrivap Concentrator, Labconco), reconstituted with 30 μL chloroform, and analyzed by GC-MS.
DNA constructs and lentiviral transductions. Generation of the pCMV6-AC-GFP lentiviral backboneexpressing TurboGFP (OriGene, PS100010) and flPPARα was described elsewhere (25). For biochemical experiments, 18 days in vitro Pparα-null hippocampal neurons were transduced with lentiviral particles at MOI 10 for 48 hours at 37°C. Viral integration was monitored by live GFP imaging.
Behavioral analysis. Barnes maze, T-maze, novel object recognition, and open-field tests were performed as described previously (see the Supplemental Methods).
Statistics. Statistical analysis was conducted using Graph Pad Prism software (version 8.2.0). Unless otherwise stated, 1-way or 2-way ANOVA was performed to determine the significance of differences between groups, followed by Bonferroni's post hoc analyses for the significance of differences among multiple experimental groups. Data are expressed as mean ± SEM or mean ± SD. P values of less than 0.05 were considered statistically significant.
Study approval. Mice were maintained and experiments conducted in accordance with NIH guidelines, and studies were approved (protocol 18-045) by the Rush University Medical Center Institutional Animal Care and Use Committee.