Bagchi M, Stohs S J
Department of Pharmaceutical Sciences, Creighton University Health Sciences Center, Omaha, NE 68178.
Free Radic Biol Med. 1993 Jan;14(1):11-8. doi: 10.1016/0891-5849(93)90504-n.
Hepatic mitochondria and microsomes as well as peritoneal macrophages from female Sprague-Dawley rats were incubated for up to 30 min at 37 degrees C in the presence of 0-200 ng/ml 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), endrin (1,2,3,4,10,10-hexachloro-6,7-epoxy-1,4,4 alpha,5,6,7,8,8 alpha-octahydroendo, endo-1,4:5,8-dimethanonaphthalene), and lindane (hexachlorocyclohexane). Production of reactive oxygen species was determined by chemiluminescence and cytochrome c reduction, while potential tissue damage was assessed by alterations in membrane fluidity. Chemiluminescence, a sensitive but nonspecific measure of free radical generation, increased 40-70% when macrophages (3 x 10(6) cells/ml), mitochondria and microsomes (1 mg/ml) were incubated with the three polyhalogenated cyclic hydrocarbons (PCH). Maximum increases in chemiluminescence occurred within 5-10 min of incubation and persisted for over 30 min. The cytochrome c reduction assay is most specific for superoxide anion production. When hepatic mitochondria were incubated with endrin and lindane for 15 min at 100 ng/ml, increases in cytochrome c reduction of 6.5- and 7.5-fold occurred, respectively, while when microsomes were incubated with these same two PCH, increases in cytochrome c reduction of 8.6- and 11.6-fold occurred, respectively. When mitochondria, microsomes, and macrophages were incubated with TCDD under identical conditions, small increases in superoxide anion production were detected. Changes in microsomal membrane fluidity were determined spectrofluorometrically following incubation with the three PCH using diphenyl-1,3,5-hexatriene as the fluorescent probe. TCDD, endrin, and lindane enhanced microsomal membrane apparent microviscosity by 2.3-, 2.1-, and 2.5-fold, respectively, indicating a significant decrease in membrane fluidity.(ABSTRACT TRUNCATED AT 250 WORDS)
将雌性斯普拉格-道利大鼠的肝线粒体、微粒体以及腹腔巨噬细胞,在37摄氏度下,于0至200纳克/毫升的2,3,7,8-四氯二苯并对二恶英(TCDD)、异狄氏剂(1,2,3,4,10,10-六氯-6,7-环氧-1,4,4α,5,6,7,8,8α-八氢内,内-1,4:5,8-二亚甲基萘)和林丹(六氯环己烷)存在的情况下孵育长达30分钟。通过化学发光和细胞色素c还原测定活性氧的产生,同时通过膜流动性的改变评估潜在的组织损伤。化学发光是自由基生成的一种敏感但非特异性的测量方法,当巨噬细胞(3×10⁶细胞/毫升)、线粒体和微粒体(1毫克/毫升)与三种多卤代环状烃(PCH)一起孵育时,化学发光增加了40 - 70%。化学发光的最大增加在孵育5 - 10分钟内出现,并持续超过30分钟。细胞色素c还原测定对超氧阴离子的产生最具特异性。当肝线粒体与异狄氏剂和林丹在100纳克/毫升下孵育15分钟时,细胞色素c还原分别增加了6.5倍和7.5倍,而当微粒体与这两种相同的PCH孵育时,细胞色素c还原分别增加了8.6倍和11.6倍。当线粒体、微粒体和巨噬细胞在相同条件下与TCDD孵育时,检测到超氧阴离子产生有小幅度增加。使用二苯基-1,3,5-己三烯作为荧光探针,在与三种PCH孵育后,通过荧光分光光度法测定微粒体膜流动性的变化。TCDD、异狄氏剂和林丹分别使微粒体膜表观微粘度增加了2.3倍、2.1倍和2.5倍,表明膜流动性显著降低。(摘要截断于250字)