Literature DB >> 15370175

Effect of melatonin cotreatment against kainic acid on coenzyme Q10, lipid peroxidation and Trx mRNA in rat hippocampus.

Ayfer Yalcin1, Emrah Kilinc, Semra Kocturk, Halil Resmi, Eser Y Sozmen.   

Abstract

Oxidative stress is a likely molecular mechanism in the neurotoxicity of kainic acid (KA), an excitotoxic substance. The aim of this report was to assess the effect of melatonin co-treatment against KA by measuring the levels of Coenzyme Q10 (CoQ 10), lipid peroxidation (LPO), and Thioredoxin (Trx) mRNA in the rat hippocampus. The male rats were divided into three groups as saline, KA treatment (15 mg/kg), and KA plus melatonin (20 mg/kg). The levels of LPO and CoQ10 were determined by high pressure liquid chromatography (HPLC) consisting of fluorescence and electro-chemical detectors, respectively. The expression of the Trx gene was quantified using reverse transcription followed by real-time polymerase chain reaction (RT-PCR). The results show that the level of LPO increased although the level of CoQ10 decreased both in homogenates and mitochondria in KA-treated rats However, melatonin co-treatment attenuated the level of LPO and partially restored the level of CoQ10. Melatonin co-treatment against KA did not affect the regulation of Trx. Finally, in the context of the decreased LPO and the increased CoQ10, the results suggest that melatonin may be protective against central nervous system pathologies involving excitotoxicity or where oxidative damage may contribute to mitochondrial dysfunction.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15370175     DOI: 10.1080/00207450490475535

Source DB:  PubMed          Journal:  Int J Neurosci        ISSN: 0020-7454            Impact factor:   2.292


  8 in total

Review 1.  Role of immune-inflammatory and oxidative and nitrosative stress pathways in the etiology of depression: therapeutic implications.

Authors:  George Anderson; Michael Berk; Olivia Dean; Steven Moylan; Michael Maes
Journal:  CNS Drugs       Date:  2014-01       Impact factor: 5.749

Review 2.  Antioxidative protection by melatonin: multiplicity of mechanisms from radical detoxification to radical avoidance.

Authors:  Rüdiger Hardeland
Journal:  Endocrine       Date:  2005-07       Impact factor: 3.633

3.  Neuroprotective effects of trans-caryophyllene against kainic acid induced seizure activity and oxidative stress in mice.

Authors:  Hao Liu; Zhi Song; Daguang Liao; Tianyi Zhang; Feng Liu; Kai Zhuang; Kui Luo; Liang Yang
Journal:  Neurochem Res       Date:  2014-11-23       Impact factor: 3.996

4.  Coenzyme q10 ameliorates neurodegeneration, mossy fiber sprouting, and oxidative stress in intrahippocampal kainate model of temporal lobe epilepsy in rat.

Authors:  Tourandokht Baluchnejadmojarad; Mehrdad Roghani
Journal:  J Mol Neurosci       Date:  2012-09-25       Impact factor: 3.444

Review 5.  Coenzyme Q10 depletion in medical and neuropsychiatric disorders: potential repercussions and therapeutic implications.

Authors:  Gerwyn Morris; George Anderson; Michael Berk; Michael Maes
Journal:  Mol Neurobiol       Date:  2013-06-13       Impact factor: 5.590

6.  Melatonin, a potent agent in antioxidative defense: actions as a natural food constituent, gastrointestinal factor, drug and prodrug.

Authors:  Rüdiger Hardeland; S R Pandi-Perumal
Journal:  Nutr Metab (Lond)       Date:  2005-09-10       Impact factor: 4.169

7.  A comparative study of the phenotype with kainic acid-induced seizure in DBA/2 mice from three different sources.

Authors:  Kyung-Ku Kang; Young-In Kim; Min-Soo Seo; Soo-Eun Sung; Joo-Hee Choi; Sijoon Lee; Young-Suk Jung; Joon Young Cho; Dae Youn Hwang; Sang-Joon Park; Kil Soo Kim
Journal:  Lab Anim Res       Date:  2020-10-28

8.  Neuroprotective effect of melatonin against kainic acid-induced oxidative injury in hippocampal slice culture of rats.

Authors:  Hyung A Kim; Kyung Hee Lee; Bae Hwan Lee
Journal:  Int J Mol Sci       Date:  2014-04-09       Impact factor: 5.923

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.