Lipids are a heterogeneous group of molecules that are critical for proper brain function1. Although recent advances in the areas of genomics and proteomics have extensively broaden our knowledge on the molecular composition of the distinct brain regions, the study of the lipidome has been lagging behind owing to technical limitations and difficulty in translating molecular profiles to cognitive function2,3,4. Increased accessibility to approaches such as mass spectrometry (MS)-based lipidomics and in vivo manipulation of lipid signaling pathways, by means of transgenic mice or viral mediated expression of lipid enzymes, currently allows a more- comprehensive overview of the role of lipids in brain function and the identification of characteristic lipid signatures associated with specific pathological conditions5,6,7,8,9.

The hippocampus is a brain structure critically involved in cognition (learning and memory) and in emotional processing. These functions are believed to be differentially regulated by subregions along the longitudinal axis of the hippocampus, from dorsal to ventral poles in rodents, or from posterior to anterior poles in humans, respectively10. A dominant view in the field implicates the dorsal hippocampus particularly in cognitive function (e.g., spatial memory), whereas the ventral hippocampus mediates emotional responses11,12,13. Although the basic intrinsic circuitry of the hippocampus is conserved along its longitudinal axis (e.g., CA1—3 and dentate gyrus), the connectivity pattern of the dorsal and ventral hippocampus is quite distinct10. In addition to dissimilar extrinsic circuitry, functional differentiation of hippocampal subregions may also be imposed through distinct autonomous cellular properties. For instance, dorsal and ventral hippocampus differ in intrinsic electrophysiological properties, such as paired pulse facilitation and the ability to induce long-term potentiation14,15. The implementation of new genomic-scale tools has redefined the anatomical boundaries of the hippocampus along its longitudinal axis16,17,18. Although the transcriptomic and proteomic landscapes of hippocampal poles have since been linked to hippocampal regional functionality, their lipid composition has not yet been topographically characterized19. Recently, differential dorsal-ventral sphingolipid metabolism was implicated in the mediation of hippocampus-dependent behavioral tasks, broadening the importance of correlating the biochemical and functional role of lipids in brain function20.

Stress can be perceived as a challenge to an individual’s homeostasis. Intense or prolonged exposure to stressors are known to elicit deleterious adaptive mechanisms, with particular functional and structural impact in the hippocampus21,22. Although stressful events are associated with a variety of mental disorders, chronic stress in rodents induces responses such as dendritic atrophy, depressive- and anxious-like behavior and learning and memory deficits22,23. A significant portion of the pathological effects of chronic stress are believed to be mediated by prolonged release of glucocorticoids (GC), namely corticosterone (CORT) in rodents. Although stress is known to induce remodeling of the hippocampal intrinsic and extrinsic circuitry, it is possible that some of the functional phenotypes may rely on a bimodal response mediated by the dorsal and ventral hippocampus, respectively. Interestingly, CORT receptors are differentially expressed along the hippocampal axis. High-affinity mineralocorticoid receptors (MR) and low-affinity GC receptors (GR) are each more highly expressed in the ventral and dorsal hippocampus, respectively24. The distinct affinity of receptors to CORT may thus explain a more-homeostatic role for MR in basal conditions and on-demand GR activation in response to increased levels of CORT. Differential receptor expression is hence instrumental for the deleterious impact of chronic stress and may underlie regional responsivity of dorsal and ventral hippocampus to stress stimuli25. Recently, we have found that a chronic unpredictable stress paradigm inversely affected dorsal and ventral hippocampus CA3 arborization (atrophy vs hypertrophy, respectively), whereas only the ventral hippocampus displayed altered synaptic plasticity, namely decreased long-term depression14. In light of additional evidence for differential responses to stimuli along the longitudinal hippocampal axis, it is therefore critical to identify new molecular pathways that determine hippocampal regional identity and plasticity, particularly in response to stress and CORT signaling.

To test whether lipid composition can also be used as a molecular marker of the distinct longitudinal anatomical sections of the hippocampus, we performed a broad-scale lipid analysis of dorsal, intermediate and ventral hippocampus and compared it with other brain areas. We found that the hippocampus shows a continuous gradient along its longitudinal axis, with a greater distinction between the dorsal and ventral subregions. Moreover, whereas CORT treatment significantly affected both regions, we found region-specific modulation of lipid species, suggesting distinct action of lipid enzymes between the dorsal and ventral hippocampus. Altogether, our findings support a biochemical model in which the hippocampus can be partitioned in subregions based on lipid composition.

Materials and methods

Animals and treatments

All animal experiments were conducted in full compliance with European Union Directive 86/609/EEC and National Institutes of Health guidelines on animal care and experimentation. Adult 2-month-old male Wistar rats (Charles River Laboratories) were housed in groups of two under standard laboratory conditions (lights on from 8:00 A.M. to 8:00 P.M.; room temperature 22 °C; ad libitum access to food and drink). Animals were assigned to daily handling (CTRL; control group); a 4-week protocol of daily subcutaneous injections with vehicle (VEH; sesame oil) or synthetic CORT (40 mg/kg) (Sigma-Aldrich)26.

Lipids analysis

Animals were killed by decapitation, brains immediately macrodissected, frozen in liquid nitrogen and stored at − 80 °C until further processing. Lipids were extracted using a modified Bligh-Dyer procedure. In brief, frozen tissue was resuspended and homogenized in 750 µL ice-cold methanol:chloroform (2:1, v/v). Phase separation was obtained by addition of 375 µL chloroform and 250 µL 1 m potassium chloride to a final solution ratio methanol:chloroform:potassium chloride 2:2.5:1 (v/v) and centrifugation for 2 min at 13,000 rpm. The lower organic phase was concentrated in a nitrogen dryer, resuspended in 15 µL chloroform and spiked with appropriate internal standards (see below) for further analysis using a 6490 Triple Quadrupole LC/MS system (Agilent Technologies), as previously described8,26. Glycerophospholipids and sphingolipids were separated using an Agilent Zorbax Rx-Sil column (diameter 2.1 × 100 mm) under an initial mobile phase A (chloroform:methanol:1 m ammonium hydroxide, 89.9:10:0.1, v/v/v) followed by phase B (chloroform:methanol:water:1 m ammonium hydroxide, 55:39.9:5:0.1, v/v/v/v); 95% A for 2 min, linear gradient to 30% A over 18 min and held for 3 min, and linear gradient to 95% A over 2 min and held for 6 min. Sterols and glycerolipids were separated with reverse-phase high-performance liquid chromatography using an isocratic mobile phase chloroform:methanol:0.1 m ammonium acetate (100:100:4v/v/v) at a flow rate of 250 μl/min with an Agilent Zorbax Eclipse XDB-C18 column (diameter 4.6 × 100 mm)8. Individual lipid species were measured by multiple reaction monitoring transitions and lipid concentration was calculated by referencing to appropriate internal standards: D5-cholesterol, CE 17:0, 4ME 16:0 diether DG, D5-TG 16:0/18:0/16:0, SM d18:1/12:0, dhSM d18:0/12:0, Cer d18:1/17:0, GalCer d18:1/12:0, LacCer d18:1/12:0, Sulf d18:1/17:0, PA 14:0/14:0, PC 14:0/14:0, PE 14:0/14:0, PG 15:0/15:0, PS 14:0/14:0, LPC 17:0, LPE 14:0, LPI 13:0, BMP 14:0/14:0 (Avanti Polar Lipids) and PI 16:0/16:0 (Echelon Biosciences). Lipid classes not internally standardized owing to commercial unavailability of respective standards were referenced to closely eluted standards. Ether-linked species (N-acyl-PS and GM3) were normalized to corresponding acyl-linked standards (PS 14:0/14:0 and PI 16:0/16:0, respectively). Lipid concentration was normalized by molar concentration across all species detected for each sample, and expressed as relative mean mol%. Lipid nomenclature follows LIPID MAPS consortium guidelines and lipid species are annotated as lipid classes followed by total number of carbons and degree unsaturation of respective acyl chains (e.g., PC 30:0)27. DG and TG species are annotated as mentioned with the addition of acyl carbon and unsaturation of the product ion (e.g., DG30:0/14:0). Sphingolipids contained d18:1 long-chain base except dhSM species, containing a d18:0 base. N-acyl-PS species contained C16:0 N-linked acyl chains. Nomenclature abbreviations are FC, free cholesterol; CE, cholesteryl ester; DG, diacylglycerol; TG, triacylglycerol; Cer, ceramide; SM, sphingomyelin; dhSM, dihydrosphingomyelin; HexCer, hexosylceramide; Sulf, sulfatides; Sulf(2OH), 2-hydroxy N-acyl sulfatide; LacCer, lactosylceramide; PA, phosphatidic acid; PC, phosphatidylcholine; PCe, ether phosphatidylcholine; PE, phosphatidylethanolamine; PEp, plasmalogen phosphatidylethanolamine; PG, phosphatidylglycerol; PI, phosphatidylinositol; PS, phosphatidylserine; LPC, lysophosphatidylcholine; LPCe, ether lysophosphatidylcholine; LPE, lysophosphatidylethanolamine; LPEp, plasmalogen lysophosphatidylethanolamine; LPI, lysophosphatidylinositol; BMP, bis(monoacylglycero)phosphate; N-acyl-PS, N-acyl-phosphatidylserine.

Statistical analysis

Statistical analysis was performed using Prism 6.0 software (Graphpad Software). Animals were randomly assigned in experimental groups. No statistical method was used to determine sample size and was based on previous studies26. Samples were blinded during tandem biochemical analysis and unblinded following data processing. Normal distribution was tested using Kolmogorov–Smirnov testing and homogeneity of group variances confirmed. All data are given as mean ± s.e.m. for a given N of biological replicates (see each figure legend for exact details). A confidence interval of 95% was assumed for all statistical tests. For comparison of two experimental conditions, unpaired two-tailed Student’s t test was performed. Descriptive statistics and individual p values are listed as Supplementary Tables. No samples or animals were excluded from analysis.


Regional lipid heterogeneity in the rodent brain

For a better understanding of the lipid composition of the rodent brain, we performed a comprehensive MS-based lipidomic analysis of distinct brain regions, namely the hippocampus, prefrontral cortex (PFC), amygdala, and cerebellum in male Wistar rats injected with VEH (see Methods for details). Based on the literature supporting molecular and functional heterogeneity along its longitudinal axis, we subdivided the hippocampus in dorsal, intermediate and ventral portions10.

In order to analyze the compositional similarity and disparity between regions, we plotted a heatmap of standard scores (Z score) of the average mol% of each lipid class per region, taking as reference value the mean of all regions pooled (Fig. 1). First, we observed a high degree of similarity, expressed as lower modular Z scores (lighter blue and red shades), between the three hippocampal regions (dorsal, intermediate, and ventral) relatively to the other three brain regions (PFC, amygdala, and cerebellum) under study. More specifically, we found the dorsal hippocampus to show higher similarity with the intermediate than the ventral hippocampus, consistent with the proposed continuous gradient of molecular identity along dorsal-ventral axis, where distinctions are more obvious between the poles16,17. The other three brain regions showed a high degree of differentiation comparatively to the hippocampal subregions and between themselves.

Fig. 1: Lipidomic analysis of brain regions from adult rats.
figure 1

Adult rats were subjected to daily injections of vehicle (VEH) and brain regions were macrodissected prior to analysis by LC-MS (see Methods for details). Heatmap generated by calculating the standard value of each lipid class (column) using as reference the pooled average relative mol% of all brain regions. Z scores [(mol% of lipid class of each animal−average mol% of lipid class of all brain regions of pool of animals)/standard deviation of average mol% lipid class of all brain regions of pool of animals] represented in gradient color; blue indicates negative Z value; red indicates positive Z value (lower and higher than reference average, respectively). Each row indicates an individual animal, per brain region (N = 9 for dorsal hippocampus, N = 10 for all other regions)

Specifically, the dorsal and intermediate hippocampus showed great enrichment in glycosphingolipids HexCer, LacCer, and Sulf. The PFC showed the highest abundance of glycerophospholipids, such as PC, PCe, PE, PEp, and lysolipid derivatives, LPCe and LPEp. The amygdala was particularly enriched in CE and LPC, whereas the cerebellum showed the highest enrichment in FC, glycosphingolipids, the atypical glycerophospholipid BMP and its precursor PG. Our findings were confirmed and validated by performing the same analysis in a previously published cohort of control adult rats (CTRL; not injected with VEH) (Supplementary Fig. 1)26. Altogether, our results highlight the heterogeneity of lipid composition between distinct brain regions and identify a continuous molecular gradient along the longitudinal axis of the hippocampus.

Distinct lipid signature of dorsal and ventral hippocampus

We subsequently focused our analysis on directly comparing the composition of the dorsal and ventral hippocampus (Fig. 2a; Supplementary Table 1). In VEH animals, the ventral hippocampus showed reduced levels of FC, as well as sphingolipids HexCer, LacCer, and Sulf and the atypical phospholipids BMP and N-acyl-PS comparatively to the dorsal hippocampus. On the contrary, the ventral hippocampus was enriched in SM and dhSM, as well as in glycerophospholipids such as PC by nearly twofold and PCe, PE, PS, LPCe, and LPE by 1.5-fold. Of note, whereas PC levels were increased, PA, both precursor and product of PC hydrolysis, was significantly decreased by ~ 20%. Importantly, overlapping results were observed in CTRL rats, with the exception of lack of significant changes between hippocampal subregions in PCe, PE (p = 0.08 and 0.06, respectively). Possibly owing to reduced levels of PE in the ventral hippocampus in CTRL rats, higher levels of LPE were not detected and LPEp were significantly reduced by 25% (Supplementary Fig. 2; Supplementary Table 2).

Fig. 2: Distinct lipid composition of dorsal and ventral hippocampus in adult rats.
figure 2

a LC-MS analysis of dorsal and ventral hippocampus macrodissected from adult rats injected with vehicle (VEH). For lipid nomenclature, see Methods section. Bar graphs indicate fold-change of average relative mol% of all lipids measured, normalized to dorsal hippocampus (mean ± SEM, N= 9 for dorsal hippocampus, N = 10 for ventral hippocampus). Upper panel, heatmap indicates individual plot of normalized average mol% of each lipid class in the ventral hippocampus. Values represented in gradient color, blue indicates below 1 and red indicates above onefold-change, respectively, normalized to dorsal hippocampus. Descriptive statistics listed in Supplementary Table 1. *p< 0.05, **p< 0.01, and ***p < 0.001 in two-tailed Student’s t test. b LC-MS analysis of diacylglycerol/glycerophospholipid and sphingolipid acyl chain. Values expressed as average mol% of total lipid measured, normalized to dorsal hippocampus. Lipids were classified per total acyl carbons and degree of unsaturation (mean ± SEM, N = 9 for dorsal hippocampus, N = 10 for ventral hippocampus). Descriptive statistics listed in Supplementary Table 2. *p< 0.05, **p< 0.01, and ***p < 0.001 in two-tailed Student’s t test

Although lipid classes are generally defined and classified by their polar head group, the acyl chains linked to their backbone show great variety in length and saturation, with important functional implications28. In general, the degree of length and saturation provides distinct physical properties to membranes, namely thickness, fluidity, and microdomain assembly29. Therefore, we analyzed the acyl composition of glycerophospholipids/DG and sphingolipids in VEH animals (Fig. 2b; Supplementary Table 3). We found that the ventral hippocampus was enriched in glycerophospholipids containing both shorter 34 carbon (C34) and over C40 acyl chains, at the significant expense of intermediate C36 and C38 chains. Moreover, glycerophospholipids from this region also showed higher abundance of poly-unsaturated chains with over 6 double bonds, at the expense of less saturated lipid species, namely containing 1–3 double bonds. Inversely, sphingolipids from the ventral hippocampus were significantly shorter, with higher abundance of C16–20 acyl chains and reduced levels of C22–26, comparatively to the dorsal portion. Contrarily to glycerophospholipids, sphingolipids were more saturated in the ventral than in the dorsal hippocampus.

Owing to the bimodal distribution of metabolically related lipids classes (e.g., PC, PA, and DG) in both experimental groups (CTRL and VEH), we directly compared the abundance of all lipid species detected by LC-MS (see Supplementary Fig. 3 for all lipid species detected). In both experimental groups, we detected an inverse profile of Cer species in the ventral and dorsal hippocampus, with longer and shorter acyl chains respectively, whereas no prominent acyl chain enrichment was detected for other sphingolipids in general. The ventral hippocampus showed significantly decreased levels for most PA species identified, particularly those with shorter acyl chains (C32–38) and decreased unsaturation (0–2 double bonds), similarly to PI species (C34–26 and 1–3 double bonds). Inversely, the ventral hippocampus was enriched in PC species with no predilection for specific acyl chain profile. Therefore, the dorsal and ventral hippocampus differ significantly in their lipid composition, with decreased levels of glycosylated sphingolipids and PA specifically in the ventral area, whereas acyl chain composition of glycerophospholipids/DG and sphingolipids vary inversely, with longer/unsaturated and shorter/saturated acyl chains, respectively.

CORT treatment affects the dorsal and ventral hippocampus differentially

Chronic stress exposure culminates in the release of GC, which mediate a myriad of pathologic effects of prolonged stress. Thus, to test whether high CORT levels modulate the lipid landscape of the hippocampus in a region-specific manner, we subjected a group of animals to daily subcutaneous injections of synthetic CORT30,31.

In the dorsal hippocampus, the most prominent change at the lipid class level was a significant near twofold increase in CE (Fig. 3a; Fig. 4a; Supplementary Table 4). Levels of LPC and BMP were decreased by 10–20% and N-acyl-PS increased by 25% (Fig. 3a; Supplementary Table 4). In addition, we found increases in multiple species of other classes of neutral lipids, namely DG and TG, though no specific acyl chain pattern was detected (Fig. 4a). We also detected multiple increases in HexCer species, with both shorter and longer acyl chains (C16–20 and C26) (Fig. 4a). Curiously, PA species showed a bimodal distribution with increases in shorter species, namely 32:0, 32:1, and 34:2, whereas 38:1 and 38:2 were decreased (Fig. 4a). Likewise, increases in shorter PI species (34:0, 34:1, 36:1, and 36:2) were identified (Fig. 4a).

Fig. 3: Effect of corticosterone injections in the lipid composition of dorsal and ventral hippocampus.
figure 3

a, b LC-MS analysis of dorsal and ventral hippocampus macrodissected from adult rats submitted to a 4-week protocol of daily injections of corticoterone (CORT) compared with age-matched control injected with vehicle (VEH). For lipid nomenclature, see Methods section. Bar graphs indicate fold-change of average relative mol% of all lipids measured, normalized to VEH (mean ± SEM, N= 9 for dorsal hippocampus of VEH; N = 10 for remaining groups). Upper panels, heatmap indicates individual plot of normalized average mol% of each lipid class in CORT-treated animals. Values represented in gradient color, blue indicates below 1 and red indicates above onefold-change, respectively, normalized to VEH. Descriptive statistics listed in Supplementary Tables 4 and 5. *p< 0.05, **p< 0.01, and ***p < 0.001 in two-tailed Student’s t test

Fig. 4: Specific lipid species are differently regulated in the dorsal and ventral hippocampus by corticosterone.
figure 4

a Lipidome profile of dorsal and ventral hippocampus from adult rats submitted to daily injections of corticosterone (CORT) compared with vehicle-treated animals (VEH). The heatmap represents all lipid species detected by LC-MS in macrodissected tissue. Lipids were classified per total acyl carbons and degree of unsaturation, respectively. For additional lipid nomenclature, see Methods section. Values represented as average fold-change of individual species in dorsal and ventral hippocampus of CORT animals, normalized to VEH (only statistically significant values shown (p < 0.05), N = 9 for dorsal hippocampus of VEH; N = 10 for remaining groups). Results were compared using two-tailed Student’s t test. b A ventral/dorsal hippocampus ratio for each lipid species detected, per animal, was calculated in adult rats injected with VEH (gray) or CORT (red) (mean ± SEM, N= 9 for VEH; N = 10 for CORT). *p< 0.05, **p< 0.01, and ***p < 0.001 in two-tailed Student’s t test

In the ventral hippocampus, CORT also induced an increase in CE and a decrease in BMP levels, matching the phenotype seen in the dorsal region (Fig. 3b; Supplementary Table 4). Concerning neutral lipids, we detected a greater number of DG species affected, as well as increased levels of TG (Fig. 3b; Fig. 4a; Supplementary Table 4). Contrarily, although HexCer species were unchanged in the ventral hippocampus, increases were found in multiple Cer and dhSM species (Fig. 4a). Specifically, overlapping acyl chain profiles were detected in the latter lipid classes, particular Cer and dhSM 22:0, 26:0, 26:1, suggesting a subset of species from these classes to be specifically regulated by CORT signaling. Notably, only longer Cer species (C20–26) were increased in ventral hippocampus, but not shorter Cer (C16–18) (Fig. 4a). Moreover, in contrast to the dorsal region in which longer PA C38 species were decreased, in the ventral hippocampus only shorter PA species were increased, namely 32:1, 34:1, and 34:2 (Fig. 4a). Finally, the same PI species (C34–36) found to be increased in the dorsal hippocampus were also upregulated in the ventral pole after CORT treatment, in addition to multiple unsaturated PS species (32:1, 34:1, 36:2, 38:3, 40:5, 40:6, and 42:5) (Fig. 4a). Concerning the acyl chain composition of glycerophospholipids/DG and sphingolipids, no significant changes were observed in the dorsal hippocampus upon CORT exposure (Fig. 3a; Supplementary Table 5), whereas the ventral hippocampus presented increased levels of glycerophospholipids/DG longer than C40 and over six double bonds, at the expense of lipids containing four double bonds (Fig. 3b Supplementary Table 5).

Considering the region-specific impact of CORT treatment in particular lipid species (e.g., DG, TG, Cer, and HexCer), we calculated the ratio of the abundance of each of the lipid species detected in both hippocampal regions and the degree of biochemical coherence between VEH and CORT animals (Fig. 4b). We found that 12 out of ~ 300 species had their coherence significantly changed (PEp 36:0, PS 32:0, LPC 16:0, LPCe 20:1, DG30:1/14:0, DG36:0/18:0, TG 56:3/18:1, Cer 24:1, dhSM 22:1, HexCer 18:1, Lac18:0, and LacCer 20:0) (Fig. 4b). Thus, our results show that elevated levels of CORT lead to major significant changes in neutral lipids in both dorsal and ventral hippocampus, whereas specific glycerophospholipids and sphingolipids species are disturbed in a region-specific manner, with more pronounced sensitivity in the ventral hippocampus in response to CORT treatment.


Here, we present the first detailed analysis of the lipid composition along the hippocampal longitudinal axis. Initially, we compared the subregions of the hippocampus (dorsal, intermediate and ventral) with other brain regions, namely the PFC, amygdala and cerebellum (Fig. 1). Consistent with the preserved intrinsic architecture of the hippocampus, we found higher similarity (i.e., less variance) between the different hippocampal subregions than other brain regions10. Importantly, we found higher similarity between the dorsal and intermediate hippocampus than its ventral component (Fig. 1). Furthermore, we found that CORT, a known mediator of chronic stress exposure, selectively impacts the lipid composition of dorsal and ventral hippocampus respectively (Figs. 3 and 4).

The comparison of the lipid composition between dorsal and ventral hippocampus in two groups of adult rats (CTRL and VEH) revealed robust and reproducible observations (Supplementary Fig. 3). Specifically, we found an enrichment for complex glycosphingolipids in the dorsal hippocampus (HexCer, Sulf and LacCer), at the expense of simpler sphingolipids (SM and dhSM). Notably, the ventral hippocampus showed increased levels of shorter Cer C16–20 and reduced levels of longer Cer C22–26. De novo sphingolipid synthesis is initiated by the action of serine palmitoyltransferase and sequential addition of an acyl chain generates Cer. Remarkably, six distinct ceramide synthases are known to catalyze the formation of multiple Cer species owing to different affinity to acyl-CoA substrates32. Our observations suggest that Cer biosynthesis in the ventral hippocampus likely depends on ceramide synthase isoforms 1 and 6, which preferably use 18:0 and 16:0 respectively. Alternatively, activation of hydroxilases or elongases in the dorsal hippocampus may account for increased longer and unsaturated Cer species (e.g., Cer C22–26). We also found that the ventral hippocampus was enriched in glycerophospholipids (PC, PCe, PE, and PS), except for PA (Fig. 2). Considering these observations, it will now be crucial to identify the mechanisms underlying regional molecular identity. A likely candidate is selective expression of lipid-metabolizing enzymes as a result of regional transcriptomic signatures, although mRNA expression does not always correlate with either protein expression or enzyme activity, also dependent on post-translational modifications and appropriate subcellular milieu for optimal function32,33. Thus, to further understand the impact of regional lipid composition, an enzyme-centric approach through the use of gain- and loss-of-function genetic and pharmacological tools may tailor designed lipid compositions to later map molecular signatures to function, such as electrophysiological plasticity or behavior20,34,35,36. To complement our approach using macrodissected tissue, future studies should implement new techniques such as matrix-assisted laser desorption/ionization imaging mass spectrometry to profile brain regions in situ, the hippocampus in particular, with cellular resolution37,38. Likewise, single-cell tissue dissociation and analysis will be crucial to resolve the individual contribution of neurons and glial cells to regional lipid distribution, as recently performed in the field of transcriptomics39,40.

Next, we studied the impact of elevated CORT levels, a critical mediator of stress commonly used as a model of depressive-like behavior41. First, CORT induced a similar upregulation of CE and TG in both hippocampal poles (Fig. 3). Interestingly, accumulation of CE is increasingly seen as a hallmark of neurodegeneration. Although, the mechanism for neutral lipid accumulation remains elusive, lipid droplet formation reportedly mitigates lipotoxicity, oxidative damage and prevents neuronal loss8,42,43,44. Merril et al.40 report a partial enrichment of CE in neuron cell bodies relatively to brain parenchyma, whereas other studies implicate glial accumulation of lipid droplets in a non-autonomous fashion as a trigger for neuronal death45. In fact, both astrocytes and microglia are also subject to GC signaling and may hence contribute to the observed changes induced by CORT46,47. Simultaneously, we observed distinct regional responses to CORT, including an increase in longer Cer C22–26 species as well as dhSM, specifically in the ventral hippocampus, whereas the dorsal hippocampus showed increased HexCer levels (Fig. 4a). These results indicate contrasting dorsal-ventral sphingolipid catabolism rather than de novo synthesis under elevated CORT levels, with a putative increase in sphingomyelinase and hydroxilase activity, promoting recycling of long Cer species in the ventral hippocampus and inhibited glucocerebrosidase and galactosidase activity in the dorsal hippocampus. In fact, previous studies implicate the sphingomyelinase-ceramide pathway in stress-induced models of depression26. Acid and neutral sphingomyelinases (ASM and NSM, respectively) are inhibited and activated in the dorsal and ventral hippocampus, respectively, in hippocampal-dependent learning, with decreased Cer 24:0 and 24:1 in ventral hippocampus during behavior extinction20. While CORT treatment decreased extinction, we detected an increase in Cer 24:1 upon CORT treatment as well as significantly impaired biochemical coherence of this Cer species when analyzing the dorsal-ventral ratio before and post treatment (Fig. 4b). Whereas increased ASM activity correlates with neurodegeneration and depressive-like behavior, GC reportedly regulate sphingolipid enzyme transcription and induce Cer accumulation, which is linked to altered cellular signaling via activation of protein phosphatase 2A and dephosphorylation of pro-survival Akt48,49. Considering GC promote gene transcription in a cell-specific manner through binding to GC response elements, a thorough search of transcription regulatory elements will be required to understand how GC modulate lipid metabolism, either directly through enzyme transcription or post-translational modifications50. This metabolic pathway is hence a suggested player in cognition and mood regulation, with both pathological and therapeutical relevance, particularly considering Cer levels can be targeted by the direct action of antidepressants51.

We also found that CORT treatment differently modulated glycerophospholipids, namely upregulating PA species in the ventral hippocampus. Our analysis revealed a partially overlapping effect of CORT, with PA 32:1 and PA 34:2 equally increased in both hippocampal poles. Not only changes in ventral hippocampus were of higher magnitude, PA 34:1 was also increased (Fig. 4a). DG species, a product of PA dephosphorylation, were also increased to a greater extent in the ventral hippocampus (Fig. 4), whereas levels of long, unsaturated PC species were specifically affected (Fig. 4a). Two possible mechanisms may account for these observations. First, PC cleavage by phospholipase D (PLD), namely isoenzymes 1 and 2, may account for increased levels in PA52. Previous studies linked PLD2 activity to modulation of PA C32–34, suggesting more prominent PLD2 recruitment in the ventral hippocampus upon CORT treatment53,54. However, increased levels of DG also suggest increased PA dephosphorylation, either as a compensatory buffering mechanism to normalize PA levels, or de novo synthesis55. Beyond the important role as fundamental precursors for phospholipid synthesis, DG and PA also act as second messengers and modulate synaptic plasticity, possibly contributing to dorsal-ventral functional dichotomy55,56. Finally, we detected a common increase in shorter and less-unsaturated PI species (34:0, 34:1, 36:1, and 36:2) in both regions. Of note, PI species not containing arachidonic or stearic acid (20:4 and 18:0, respectively) not only are less abundant but also not as readily convertible to polyphosphorylation, possibly inhibiting cellular signaling (e.g., via Akt)57,58. A possible explanation for such observation is distinct acyl chain incorporation in PI synthesis by enzyme modulation (DG kinases or CDP-diacylglycerol synthases). However, considering the low abundance of these species, acyl chain enrichment may instead depend on subcellular lipid remodeling, namely via inhibition of acyltransferases, such as LYCAT and LPIAT1, responsible for incorporating stearic and arachidonic acid, respectively59,60. Considering that manipulation of PI acyl chain disrupts brain morphology and function, future studies should address the abundance of free fatty acids to clarify substrate availability for lipid mediators61,62.

In summary, our study reveals a distinct lipid composition along the longitudinal axis of the hippocampus. We validate the ventral hippocampus as more sensitive to lipid modulation by CORT, in line with previous reports of increased regional synaptic plasticity and susceptibility to other stressors, such as kainate-induced seizures14,63,64. Thus, the distribution of lipids and enzymes across brain regions may determine regional susceptibility to distinct neurological disorders. This view privileges the prioritization of designed therapeutical approaches for different conditions using enzyme inhibition, replacement or silencing therapies or dietary manipulations65. A currently promising approach is the modulation of sphingolipids and glycerophospholipids in mood disorders, namely through pharmacological usage of functional inhibitors of acid sphingomyelinase and antidepressants, respectively66,67. Altogether, a thorough knowledge of hippocampal subregional identity will provide new tools to understand and manipulate each region’s function, both in health and disease.