2010
DOI: 10.1016/j.bbr.2009.10.024
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Silibinin attenuates cognitive deficits and decreases of dopamine and serotonin induced by repeated methamphetamine treatment

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Cited by 81 publications
(47 citation statements)
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“…On the other hand, dopamine and serotonin levels gave positive results via S. marianum seeds extract or S. marianum seeds oil fraction treatment for irradiated rats. In the case of pharmacological stress caused by methamphetamine treatment, silibinin attenuated the decreases of dopamine levels in the prefrontal cortex and serotonin levels in the hippocampus [46]. Silymarin showed an antioxidant effect in the central nervous system, being able to cross the blood-brain barrier [47].…”
Section: Discussionmentioning
confidence: 99%
“…On the other hand, dopamine and serotonin levels gave positive results via S. marianum seeds extract or S. marianum seeds oil fraction treatment for irradiated rats. In the case of pharmacological stress caused by methamphetamine treatment, silibinin attenuated the decreases of dopamine levels in the prefrontal cortex and serotonin levels in the hippocampus [46]. Silymarin showed an antioxidant effect in the central nervous system, being able to cross the blood-brain barrier [47].…”
Section: Discussionmentioning
confidence: 99%
“…for 10 days, once per day (09:00). Saline-withdrawn and METH-withdrawn animals were treated with the same administration paradigm and left to spontaneously withdraw in their home-cages for a period of 7 days (unless otherwise stated), as previously described (Lu et al, 2010).…”
Section: Chronic Steady-dose Methamphetamine Administration Paradigmmentioning
confidence: 99%
“…However, chronic, rather than acute, administration of moderate doses (p2 mg/kg daily) can impair cognitive performance, including measures of working memory (Lee et al, 2011;Nagai et al, 2007) and object recognition memory (Arai et al, 2009;Ito et al, 2007;Noda et al, 2010). In fact, administering mice 1 mg/kg of MA daily for 7 days produces reliable deficits in object recognition memory even when assessed at least 1 week after drug cessation (Kamei et al, 2006;Lu et al, 2010;Mizoguchi et al, 2011).…”
Section: Animals Exposed To Ma Will Show Cognitive Decline Particulamentioning
confidence: 99%
“…In animals, in addition to cognitive decline produced by chronic moderate (p2 mg/kg daily) or escalating doses of MA, concomitant alterations have been observed in D2-like dopamine receptor and dopamine transporter binding (DAT) (Groman et al, 2012), tissue levels of dopamine and serotonin (Lu et al, 2010), NMDA receptor binding (Lee et al, 2011), glutamate receptor (mGluR5) expression (Reichel et al, 2011), pyramidal neuron cell firing (Parsegian et al, 2011), and novelty-induced hyperphosphorylation of extracellular signal-related kinase 1/2 (Ito et al, 2007;Kamei et al, 2006;Nagai et al, 2007). In humans, cross-sectional studies likewise show differences in the brain structure and function between MA-dependent and healthy control participants (for reviews, see Berman et al (2008); Chang et al (2007); Salo and Fassbender (2012)).…”
Section: Ma Abuse Will Be Associated With Changes In the Human Brainmentioning
confidence: 99%