Tulsawani Rajkumar, Bhattacharya R
Division of Pharmacology and Toxicology, Defence Research and Development Establishment, Jhansi Road, Gwalior, 474002, MP, India.
Biomed Environ Sci. 2006 Feb;19(1):61-6.
To investigate the biochemical changes in rat brain and liver following acute exposure to a lethal dose of cyanide, and its response to treatment of alpha-ketoglutarate (alpha-KG) in the absence or presence of sodium thiosulfate (STS).
Female rats were administered 2.0 LD50 potassium cyanide (KCN; oral) in the absence or presence of pre-treatment (-10 min), simultaneous treatment (0 min) or post-treatment (+2-3 min) of alpha-KG (2.0 g/kg, oral) and/or STS (1.0 g/kg, intraperitoneal, -15 min, 0 min or + 2-3 min). At the time of onset of signs and symptoms of KCN toxicity (2-4 min) and at the time of death (5-15 min), various parameters particularly akin to oxidative stress viz. cytochrome oxidase (CYTOX), superoxide dismutase (SOD), glutathione peroxidase (GPx), reduced glutathione (GSH) and oxidized glutathione (GSSG) in brain, and CYTOX, sorbitol dehydrogenase (SDH), alkaline phosphatase (ALP), GSH and GSSG in liver homogenate were measured.
At both time intervals brain CYTOX, SOD, GPx, and GSH significantly reduced (percent inhibition compared to control) to 24%, 56%, 77%, and 65%, and 44%, 46%, 78%, and 57%, respectively. At the corresponding time points liver CYTOX and GSH reduced to 74% and 63%, and 44% and 68%, respectively. The levels of GSSG in the brain and liver, and hepatic ALP and SDH were unchanged. Pre-treatment and simultaneous treatment of a-KG alone or with STS conferred significant protection on above variables. Post-treatment was effective in restoring the changes in liver but failed to normalize the changes in the brain.
Oral treatment with alpha-KG alone or in combination with STS has protective effects on cyanide-induced biochemical alterations in rat brain and liver.
研究大鼠急性暴露于致死剂量氰化物后大脑和肝脏的生化变化,以及在有无硫代硫酸钠(STS)的情况下其对α-酮戊二酸(α-KG)治疗的反应。
雌性大鼠在无预处理(-10分钟)、同时处理(0分钟)或后处理(+2 - 3分钟)α-KG(2.0克/千克,口服)和/或STS(1.0克/千克,腹腔注射,-15分钟、0分钟或+2 - 3分钟)的情况下,给予2.0倍半数致死量的氰化钾(KCN;口服)。在出现KCN毒性的体征和症状时(2 - 4分钟)以及死亡时(5 - 15分钟),测量各种与氧化应激特别相关的参数,即大脑中的细胞色素氧化酶(CYTOX)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)、还原型谷胱甘肽(GSH)和氧化型谷胱甘肽(GSSG),以及肝脏匀浆中的CYTOX、山梨醇脱氢酶(SDH)、碱性磷酸酶(ALP)、GSH和GSSG。
在两个时间间隔,大脑中的CYTOX、SOD、GPx和GSH均显著降低(与对照组相比的抑制百分比),分别降至24%、56%、77%和65%,以及44%、46%、78%和57%。在相应时间点,肝脏中的CYTOX和GSH分别降至74%和63%,以及44%和68%。大脑和肝脏中的GSSG水平以及肝脏中的ALP和SDH未发生变化。单独或与STS联合对α-KG进行预处理和同时处理,对上述变量具有显著的保护作用。后处理在恢复肝脏变化方面有效,但未能使大脑变化恢复正常。
单独口服α-KG或与STS联合使用对氰化物诱导的大鼠大脑和肝脏生化改变具有保护作用。