Abstract

Although depression is one of the prevailing central nervous system disorders, there is still not enough knowledge about the exact alterations underlying its pathophysiology and the treatment is often inefficient. Our study aims at exploring a potential relationship between major depressive disorder and the purinergic P2X7 receptor (P2X7R), since in previous behavioural tests P2rx7 knock out mice displayed an antidepressant-like phenotype. Among many other known symptoms, the loss of hippocampal spine synapses is a revealing feature of the disorder. Therefore we wanted to measure the density of spine synapses in the molecular layer of the dentate gyrus in the learned helplessness paradigm and later see if genetic inhibition of P2X7R could have influence on this condition. Wild type C57Bl/6 and P2rx7 knock out male mice were exposed to inescapable footshocks (IES) in shuttle boxes during 2 training days and on the 3rd day learned helplessness was tested, where helpless animals usually failed to escape. Control animals were also placed in shuttle boxes but did not receive footshocks until testing. Escape failures and the latency to escape were measured to determine helpless behaviour. Electron microscopy analysis was performed to determine spine synapse density in the different groups. In wild type mice both average escape latency and the number of failed escapes were significantly higher in the IES treated group, however, we could not find such divergency in P2rx7 knock out mice. Electron microscopy analysis confirmed alterations in spine synapse density in the molecular layer of the dentate gyrus subsequent to learned helplessness experiments, as results indicated a significant decrease in spine synapse density in wild type mice, but not in knock out animals. These findings may lead to presume a role of the P2X7 receptor in this disorder and further experiments will hopefully help get a better understanding and thus more effective treatment of major depression.

Highlights

  • Alzheimer’s disease (AD) is an incurable neurodegenerative disease characterized by progressive dementia

  • The results of the present study indicate that development of the neuronal hypoxic tolerance induced by the three-trial, in contrast to one-trial, mild hypoxic preconditioning is apparently largely associated with the activation of CREB, as well as brain-derived neurotrophic factor (BDNF) and Bcl-2 overexpression

  • No significant differences in serum level of Solubile form of RAGE (sRAGE) where found between rapidly progressing and slow progressing subgroup of multiple sclerosis (MS) patients.Our results suggest for the role of sRAGE in MS ethiopathogenesis, but we did not find any association of sRAGE in serum with the rate of MS disability progression

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Summary

Introduction

Alzheimer’s disease (AD) is an incurable neurodegenerative disease characterized by progressive dementia. The aim of the study was to characterize the effects of streptozocin (STZ)-indced diabetes on learning and memory of 5XFAD and wild-type (WT) mice in Morris water maze (MWM) at ages 2 and 6 months and on brain amyloid load. Existing evidence suggests GABAergic system is involved in pathophysiology of Alzheimer’s disease (AD) via inhibitory interneuron deficits (Verret et al, 2012) and decrease in functional GABAA receptors (Limon et al, 2012). Our concept: low doses of muscimol may prevent learning/memory deficits in intracerebroventricular (icv) streptozocin (STZ)-induced AD nontransgenic rat model. The Sigma-1 receptor is a chaperone protein that modulates intracellular calcium signalling of the endoplasmatic reticulum and is involved in learning and memory processes.The aim of the present study was to compare in vitro Ca2+ concentration modulating activity and in vivo behavioural effects of enantiomers of methylphenylpiracetam, a novel positive allosteric modulator of Sigma-1 receptors

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