2019
DOI: 10.1016/j.ntt.2019.02.002
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Repeated toluene exposure alters the synaptic transmission of layer 5 medial prefrontal cortex

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Cited by 11 publications
(8 citation statements)
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“…The effects of inhalants on the central nervous system (CNS), including cognition, have been relatively well studied, and it is thought that inhibited N ‐methyl‐D‐aspartate (NMDA) receptor signaling and region‐specific changes to glutamatergic and gamma‐Aminobutyric acid (GABA)‐ergic signaling underpin these effects . However, inhalants can also have a wide range of peripheral effects throughout the body, including on the renal, cardiovascular, and pulmonary systems .…”
Section: The Effects Of Inhalant Abuse On Energy Balancementioning
confidence: 58%
“…The effects of inhalants on the central nervous system (CNS), including cognition, have been relatively well studied, and it is thought that inhibited N ‐methyl‐D‐aspartate (NMDA) receptor signaling and region‐specific changes to glutamatergic and gamma‐Aminobutyric acid (GABA)‐ergic signaling underpin these effects . However, inhalants can also have a wide range of peripheral effects throughout the body, including on the renal, cardiovascular, and pulmonary systems .…”
Section: The Effects Of Inhalant Abuse On Energy Balancementioning
confidence: 58%
“…This is in accordance with Scheepers research entitled Assessment of Exposure of Gas Station Attendants in Sri Lanka to Benzene, Toluene and Xylene (BTX) with a reduction in work duration to 40 hours/week can reduce BTX concentrations in workers' blood to safe limits 9 . Repeated toluene exposure can cause cognitive impairment in mice 10 . Based on table 2, the average glutathione concentration in the Osowilangun shoe home industry workers was 35,655 µg/L.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, CIT‐induced downregulation of critical plasticity genes may also reflect altered mPFC physiology as two acute exposures to toluene (10 500 ppm) in adolescent but not adult rats alter the intrinsic excitability of mPFC neurons projecting to the NAc 6 . Thus, future studies that focus on the consequences of adolescent CIT exposure upon mPFC neurophysiology and the responsivity of the mPFC transcriptome to subsequent stimuli (e.g., additional toluene exposure or learning) are warranted, particularly in light of recent findings that N ‐methyl‐ d ‐aspartate (NMDA)‐mediated plasticity within the mPFC may underlie the cognitive deficits associated with CIT 43 . Moreover, future studies should functionally validate the role of identified candidate genes in CIT‐induced cognitive deficits employing viral‐mediated gene knock‐down or overexpression within the mPFC, although this is beyond the scope of the present study.…”
Section: Discussionmentioning
confidence: 99%