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dc.contributor.authorSwanepoel, Twanette
dc.contributor.authorMöller, Marisa
dc.contributor.authorHarvey, Brian Herbert
dc.date.accessioned2017-11-20T07:14:41Z
dc.date.available2017-11-20T07:14:41Z
dc.date.issued2018
dc.identifier.citationSwanepoel, T. et al. 2018. N-acetyl cysteine reverses bio-behavioural changes induced by prenatal inflammation, adolescent methamphetamine exposure and combined challenges. Psychopharmacology, 235(1):351-368. [https://doi.org/10.1007/s00213-017-4776-5]en_US
dc.identifier.issn0033-3158
dc.identifier.issn1432-2072 (Online)
dc.identifier.urihttp://hdl.handle.net/10394/26081
dc.identifier.urihttps://link.springer.com/article/10.1007/s00213-017-4776-5
dc.identifier.urihttps://doi.org/10.1007/s00213-017-4776-5
dc.description.abstractRationale Schizophrenia is associated with prenatal inflammation and/or postnatal stressors such as drug abuse, resulting in immune-redox dysfunction. Antioxidants may offer therapeutic benefits. Objectives The objective of this study is to investigate N-acetyl cysteine (NAC) as a therapeutic antioxidant to reverse schizophrenia-like bio-behavioural changes in rats exposed to maternal immune activation (MIA), adolescent methamphetamine (MA) or a combination thereof. Methods Sprague-Dawley offspring prenatally exposed to saline/lipopolysaccharide (LPS) received saline or MA (0.2–6 mg kg−1 twice daily × 16 days) during adolescence and divided into LPS, MA and LPS + MA groups. Vehicle/NAC (150 mg kg−1 × 14 days) was administered following MA/saline exposure on postnatal day 51–64. Social interaction, novel object recognition and prepulse inhibition (PPI) of startle, as well as regional brain monoamines, lipid peroxidation, plasma reactive oxygen species (ROS) and pro- and anti-inflammatory cytokines (TNF-α; IL-10), were assessed. Results NAC reversed LPS, MA and LPS + MA-induced anxiety-like social withdrawal behaviours, as well as MA and LPS + MA-induced deficits in recognition memory. PPI deficits were evident in MA, LPS and LPS + MA models, with NAC reversing that following LPS + MA. NAC reversed LPS, MA and LPS + MA-induced frontal cortical dopamine (DA) and noradrenaline (NA) elevations, LPS and LPS + MA-induced frontal cortical 3,4-dihydroxyphenylacetic acid (DOPAC), serotonin (5-HT) and striatal NA deficits as well as LPS + MA-induced frontal cortical 5-HT turnover. Decreased IL-10 in the LPS, MA and LPS + MA animals, and increased TNF-α in the LPS and MA animals, was reversed with NAC. NAC also reversed elevated lipid peroxidation and ROS in the LPS and LPS + MA animals. Conclusions Prenatal LPS, LPS + postnatal MA challenge during adolescence, and to a lesser extent MA alone, promotes schizophrenia-like bio-behavioural changes later in life that are reversed by NAC, emphasizing therapeutic potential for schizophrenia and MA-associated psychosis. The nature and timing of the dual-hit are criticaen_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.subjectPsychosisen_US
dc.subjectPrenatal infectionen_US
dc.subjectMethamphetamineen_US
dc.subjectN-acetyl cysteineen_US
dc.subjectNeurodevelopmental modelen_US
dc.subjectDual-hiten_US
dc.titleN-acetyl cysteine reverses bio-behavioural changes induced by prenatal inflammation, adolescent methamphetamine exposure and combined challengesen_US
dc.typeArticleen_US
dc.contributor.researchID21700486 - Swanepoel, Twanette
dc.contributor.researchID21247250 - Möller Wolmarans, Marisa
dc.contributor.researchID11083417 - Harvey, Brian Herbert


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