Prenatal THC exposure induces long-term, sex-dependent cognitive dysfunction associated with lipidomic and neuronal pathology in the prefrontal cortex-hippocampal network.
Mohammed H SarikahyaSamantha L CousineauMarta De FeliceHanna J SzkudlarekKaren K W WongMarieka V DeVuonoKendrick LeeMar Rodríguez-RuizDana GummersonEmma ProudTsun Hay Jason NgRoger HudsonTony JungDaniel B HardyKen K-C YeungSusanne SchmidWalter RushlowSteven R LaviolettePublished in: Molecular psychiatry (2023)
With increasing maternal cannabis use, there is a need to investigate the lasting impact of prenatal exposure to Δ9-tetrahydrocannabinol (THC), the main psychotropic compound in cannabis, on cognitive/memory function. The endocannabinoid system (ECS), which relies on polyunsaturated fatty acids (PUFAs) to function, plays a crucial role in regulating prefrontal cortical (PFC) and hippocampal network-dependent behaviors essential for cognition and memory. Using a rodent model of prenatal cannabis exposure (PCE), we report that male and female offspring display long-term deficits in various cognitive domains. However, these phenotypes were associated with highly divergent, sex-dependent mechanisms. Electrophysiological recordings revealed hyperactive PFC pyramidal neuron activity in both males and females, but hypoactivity in the ventral hippocampus (vHIPP) in males, and hyperactivity in females. Further, cortical oscillatory activity states of theta, alpha, delta, beta, and gamma bandwidths were strongly sex divergent. Moreover, protein expression analyses at postnatal day (PD)21 and PD120 revealed primarily PD120 disturbances in dopamine D1R/D2 receptors, NMDA receptor 2B, synaptophysin, gephyrin, GAD67, and PPARα selectively in the PFC and vHIPP, in both regions in males, but only the vHIPP in females. Lastly, using matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI IMS), we identified region-, age-, and sex-specific deficiencies in specific neural PUFAs, namely docosahexaenoic acid (DHA) and arachidonic acid (ARA), and related metabolites, in the PFC and hippocampus (ventral/dorsal subiculum, and CA1 regions). This study highlights several novel, long-term and sex-specific consequences of PCE on PFC-hippocampal circuit dysfunction and the potential role of specific PUFA signaling abnormalities underlying these pathological outcomes.
Keyphrases
- prefrontal cortex
- mass spectrometry
- cerebral ischemia
- working memory
- pregnant women
- spinal cord
- high resolution
- liquid chromatography
- traumatic brain injury
- subarachnoid hemorrhage
- single cell
- preterm infants
- brain injury
- high fat diet
- oxidative stress
- adipose tissue
- high performance liquid chromatography
- mild cognitive impairment
- neuropathic pain
- risk assessment
- deep brain stimulation
- skeletal muscle
- climate change
- capillary electrophoresis
- cognitive impairment
- functional connectivity
- gas chromatography
- multiple sclerosis
- preterm birth
- human health
- weight gain
- glycemic control
- photodynamic therapy