甲氰菊酯对鲤鳃Na+-K+-ATP酶活性及组织损伤的影响

Effect of Fenpropathrin on Na+-K+-ATPase and histomorphology of Cyprinus carpio gills

  • 摘要: 采用半静止染毒法, 探讨甲氰菊酯对鲤(Cyprinus carpio)的急性毒性和对鳃组织Na+-K+-ATP酶活性的影响及组织的病理损伤。急性毒性结果表明, 甲氰菊酯对鲤的96 h半致死质量浓度(LC50)为8.53 μg·L-1, 安全质量浓度(SC)为0.853 μg·L-1。设置1/2 96 h LC50以下的5个质量浓度0、0.43 μg·L-1、0.85 μg·L-1、1.71 μg·L-1、4.27 μg·L-1作用于鲤21 d, 分别在第1、第3、第7、第14和第21天采集组织样品进行酶活测定以及组织病理学观察。结果表明, 鳃组织中Na+-K+-ATP酶活性随着暴露时间的推移其动态变化呈先下降后上升、之后又有所回落的趋势。暴露第3天各组酶活性降至最低点, 与对照组相比差异极显著(P < 0.01), 其抑制率分别达到42.49%、27.48%、59.03%和46.31%;第14天各组酶活达最高值并显著(P < 0.05)或极显著(P < 0.01)高于对照组; 第21天除最高浓度组显著低于对照组外, 其余3组仍高于对照组。H-E染色显示, 鳃组织学损伤主要是鳃小片扭曲, 上皮细胞和柱状细胞脱落, 鳃小片毛细血管扩张充血, 粘液细胞和基部细胞增生, 严重时鳃小片粘连, 呈棍棒状病变。以上损伤具有剂量相关性和时间积累效应。

     

    Abstract: The study explores the effect of Fenpropathrin on the acute toxicity and Na+-K+-ATPase activity and histopathological changes of carp (Cyprinus carpio) gills.According to the acute toxicity result, the 96 hour lethal concentration (96 h LC50) is 8.53 μg·L-1and the safe concentration (SC) is 0.853 μg·L-1.Exposed to Fenpropathrin at concentrations of 0, 0.43 μg·L-1, 0.85 μg·L-1, 1.70 μg·L-1 and 4.27 μg·L-1, the gill tissue of carp were collected at the 1st, 3rd, 7th, 14th, 21st day, respectively.Results indicate that the activities of Na+-K+-ATP enzyme in gill tissue during different exposure periods vary in a wave shape, i.e., first decrease, then increase, and decrease again as the exposing time progresses at the same concentration.The ATPase activities reach the lowest at 3rd day, which are very significantly different from the control (P < 0.01), with inhibition rates of 42.49%, 27.48%, 59.03% and 46.31%, respectively.The enzyme activities of all concentration groups reach the highest at 14th day, which are significantly (P < 0.05) or very significantly (P < 0.01) higher than that of the control. At 21st day, the enzyme activities of the highest concentration group are significantly lower than that of the control except the other 3 concentration groups.The HE staining histological changes in the gills include gill-amells distortion, epithelial cell and pillar cell shedding, blood capillary of gill-amells expanding and hyperaemia, mucilage cell and basal cell hyperplasia, sometimes even gill-amells adhesion and gill filament becoming club-shape.The damages of gill are related to concentration and effect of time accumulation.

     

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