Nony P A, Scallet A C, Rountree R L, Ye X, Binienda Z
National Center for Toxicological Research, USFDA, Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Jefferson 72079, USA.
Metab Brain Dis. 1999 Jun;14(2):83-94. doi: 10.1023/a:1020753629477.
3-Nitropropionic acid (3-NPA) is a toxin sometimes produced on moldy crops (sugarcane, peanuts, etc.) in amounts sufficient to cause severe neurological disorders when consumed by humans. In vitro, 3-NPA irreversibly inactivates SDH, a Complex II respiratory enzyme required for mitochondrial energy production. A single dose of 3-NPA (30 mg/kg s.c.) was given to singly-caged adult male Sprague-Dawley rats. Rectal temperature was measured after dosing as a potential biomarker of exposure to 3-NPA, and animals were sacrificed at various times after 3-NPA exposure for histochemical visualization of SDH activity. 3-NPA-treated rats experienced a progressive hypothermia, which reached a loss of 3 degrees C or more in core body temperature by 3 hours after dosing. The optical density of the SDH stain in brain was reduced according to a similar time-course, most prominently in the cerebellum and least sharply in the thalamus. The caudate nucleus had the greatest density of SDH staining that we measured in brain; it also has been reported to be the region most consistently lesioned by 3-NPA. However, within other areas of brain such as subdivisions of the hippocampus, neither endogenous SDH activity nor its sensitivity to inhibition by 3-NPA could predict the susceptibility to neurodegenerative changes. Although SDH activity remained significantly reduced in most areas of brain (except thalamus) for up to 5 days after dosing, core temperatures had returned to control values by 5 days suggesting that animals can utilize an alternate method of heat production to withstand insult by 3-NPA.
3-硝基丙酸(3-NPA)是一种有时在发霉作物(甘蔗、花生等)上产生的毒素,当被人类食用时,其产生量足以导致严重的神经紊乱。在体外,3-NPA会不可逆地使琥珀酸脱氢酶(SDH)失活,SDH是线粒体能量产生所需的一种复合体II呼吸酶。给单笼饲养的成年雄性Sprague-Dawley大鼠单次注射3-NPA(30毫克/千克,皮下注射)。给药后测量直肠温度,作为接触3-NPA的潜在生物标志物,并在3-NPA暴露后的不同时间处死动物,以进行SDH活性的组织化学可视化观察。经3-NPA处理的大鼠出现渐进性体温过低,给药后3小时核心体温下降3摄氏度或更多。大脑中SDH染色的光密度根据类似的时间进程降低,在小脑中最明显,在丘脑中最不明显。尾状核具有我们在大脑中测量到的最高SDH染色密度;据报道,它也是3-NPA最常损伤的区域。然而,在大脑的其他区域,如海马体的亚区,内源性SDH活性及其对3-NPA抑制的敏感性均无法预测对神经退行性变化的易感性。尽管给药后长达5天大脑的大多数区域(除丘脑外)SDH活性仍显著降低,但核心体温在5天时已恢复到对照值,这表明动物可以利用另一种产热方法来抵御3-NPA的损伤。