Literature DB >> 21781919

Sex differences in dizocilpine (MK-801) neurotoxicity in rats.

G H Hur1, W C Son, S Shin, J K Kang, Y B Kim.   

Abstract

The sex differences in the clinical signs and the distribution of astrocytic glial fibrillary acidic protein (GFAP) induced by an N-methyl-d-aspartate antagonist, dizocilpine (MK-801), were examined. A single intraperitoneal injection of MK-801 (5 mg/kg body weight) caused a prolonged recumbency (35-40 h), leading to a severe loss of body weight in female rats, in contrast to a light effect in males, independent of age. Early salivation or lacrimation was also severe in females and delayed bloody lacrimation was observed in females only. The pretreatment with 17β-estradiol (0.1 or 1.0 mg/kg body weight) made early signs worse in both sexes, but a remarkable mortality (20-40%) was observed in females only. The treatment with MK-801 greatly enhanced GFAP expression in retrospenial cortex of both sexes with a higher enhancement in females. The MK-801-induced expression of GFAP was further increased by the pretreatment with 17β-estradiol (1 mg/kg body weight) in females. Overall, the expression of GFAP in the retrospenial cortex of rats treated with MK-801 appeared to be higher in females than males, somewhat in parallel with more severe clinical signs in females. The results indicate the higher sensitivity of female rats to MK-801 neurotixicity, and the possible involvement of 17β-estradiol in the sex differences of the sensitivity.

Entities:  

Year:  1999        PMID: 21781919     DOI: 10.1016/s1382-6689(99)00003-4

Source DB:  PubMed          Journal:  Environ Toxicol Pharmacol        ISSN: 1382-6689            Impact factor:   4.860


  6 in total

1.  Effects of amphetamine exposure in adolescence or young adulthood on inhibitory control in adult male and female rats.

Authors:  Lindsey R Hammerslag; Alex J Waldman; Joshua M Gulley
Journal:  Behav Brain Res       Date:  2014-01-22       Impact factor: 3.332

Review 2.  Clinical physiology and mechanism of dizocilpine (MK-801): electron transfer, radicals, redox metabolites and bioactivity.

Authors:  Peter Kovacic; Ratnasamy Somanathan
Journal:  Oxid Med Cell Longev       Date:  2010 Jan-Feb       Impact factor: 6.543

3.  Adult and adolescent C57BL/6J and DBA/2J mice are differentially susceptible to fear learning deficits after acute ethanol or MK-801 treatment.

Authors:  L R Seemiller; T J Gould
Journal:  Behav Brain Res       Date:  2021-05-08       Impact factor: 3.352

4.  Involvement of NMDA receptors containing the GluN2C subunit in the psychotomimetic and antidepressant-like effects of ketamine.

Authors:  Mireia Tarrés-Gatius; Lluís Miquel-Rio; Leticia Campa; Francesc Artigas; Anna Castañé
Journal:  Transl Psychiatry       Date:  2020-12-10       Impact factor: 6.222

5.  REL-1017 (Esmethadone), A Novel NMDAR Blocker for the Treatment of MDD is Not Neurotoxic in Sprague-Dawley Rats.

Authors:  Francesco Bifari; Marco Pappagallo; Michael Bleavins; Sergio Traversa; Franco Folli; Paolo L Manfredi
Journal:  Front Pharmacol       Date:  2022-04-25       Impact factor: 5.810

6.  Effect of Neonatal Treatment With the NMDA Receptor Antagonist, MK-801, During Different Temporal Windows of Postnatal Period in Adult Prefrontal Cortical and Hippocampal Function.

Authors:  Maria E Plataki; Konstantinos Diskos; Christos Sougklakos; Marouso Velissariou; Alexandros Georgilis; Vasiliki Stavroulaki; Kyriaki Sidiropoulou
Journal:  Front Behav Neurosci       Date:  2021-06-11       Impact factor: 3.558

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.