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Deficient brain GABA metabolism leads to widespread impairments of astrocyte and oligodendrocyte function

ABSTRACT: Loss of function of the enzyme succinic semialdehyde dehydrogenase (SSADH) impairs metabolism of the inhibitory neurotransmitter GABA. This neurometabolic disorder, known as SSADH deficiency, leads to great neurochemical imbalances and severe neurological symptoms, including cognitive deficits and seizures. Despite the known identity of the enzymatic deficit, the underlying pathology of SSADH deficiency remain unclear. To uncover new mechanisms of the disease, we here provide an integrative analysis of cerebral protein expression, functional metabolism and lipid composition in a genetic mouse model of SSADH deficiency (ALDH5A1 knock-out mice). Our proteomic analysis revealed a clear regional vulnerability, as protein alterations primarily manifested in the hippocampus and cerebral cortex of the ALDH5A1 knock-out mice. These regions displayed aberrant expression of multiple proteins linked to amino acid homeostasis, mitochondria, glial function and myelination. Stable isotope tracing in acutely isolated brain slices demonstrated an overall maintained oxidative metabolism of glucose, but a selective decrease in astrocyte metabolic activity in the cerebral cortex of ALDH5A1 knock-out mice. In contrast, an elevated capacity of oxidative glutamine metabolism was observed in the ALDH5A1 knock-out mice, which may serve as a metabolic compensation of impaired astrocyte glutamine synthesis. In addition to reduced expression of critical oligodendrocyte proteins, a severe depletion of myelin-enriched sphingolipids was found in the ALDH5A1 knock-out brain, suggesting dysregulation or degeneration of myelin. Our study highlight that impaired astrocyte and oligodendrocyte function may play crucial roles in SSADH deficiency pathology, strongly warranting an exploration of the therapeutic potential of these cells.

INSTRUMENT(S): timsTOF Pro

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Brain

DISEASE(S): Succinic Semialdehyde Dehydrogenase Deficiency

SUBMITTER: Niels Henning Skotte

LAB HEAD: Niels Henning Skotte

PROVIDER: PXD051032 | Pride | 2024-06-26

REPOSITORIES: Pride

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			Action	DRS
	20220218_TIMS1_nLC13_FLQ_SA_120min_200ng_DIA_ALDH5A1-Cov-01-Ctx01_A1_1_5558.d.7z	Other
	20220218_TIMS1_nLC13_FLQ_SA_120min_200ng_DIA_ALDH5A1-Cov-02-Ctx02_A2_1_5559.d.7z	Other
	20220218_TIMS1_nLC13_FLQ_SA_120min_200ng_DIA_ALDH5A1-Cov-03-Ctx03_A3_1_5560.d.7z	Other
	20220218_TIMS1_nLC13_FLQ_SA_120min_200ng_DIA_ALDH5A1-Cov-04-Ctx04_A4_1_5561.d.7z	Other
	20220218_TIMS1_nLC13_FLQ_SA_120min_200ng_DIA_ALDH5A1-Cov-05-Ctx05_A5_1_5562.d.7z	Other

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Deficient brain GABA metabolism leads to widespread impairments of astrocyte and oligodendrocyte function

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