Tissue Distribution and Depuration of the Extracted Hepatotoxic Cyanotoxin Microcystins in Crucian Carp (Carassius carassius) Intraperitoneally Injected at a Sublethal Dose. (2008)

• Record Type: Journal Article
• Authors: Lei, Hehua; Xie, Ping; Chen, Jun; Liang, Gaodao; Yu, Ting; Jiang, Yan
• Other Names: Sonesten Lars Academic Editor.
• Is Part Of: TheScientificWorldjournal. Volume 8(2008)
• Page Start: 713
• Page End: 719
• Publication Date: 2008
• Subjects: microcystins -- intraperitoneal injection -- crucian carp -- tissue distribution -- depuration; Science -- Periodicals; Technology -- Periodicals; Medicine -- Periodicals; 505
• DOI: 10.1100/tsw.2008.101
• Languages: English
• ISSNs: 2356-6140

Abstract

Abstract : An acute toxicity experiment was conducted by intraperitoneal injection with a sublethal dose of extracted microcystins (MCs), 50 μg MC-LR (where L = leucine and R = arginine) equivalent/kg body weight (BW), to examine tissue distribution and depuration of MCs in crucian carp ( Carassius carassius ). Liver to body weight ratio increased at 3, 12, 24, and 48 h postinjection compared with that at 0 h ( p < 0.05). MC concentrations in various tissues and aquaria water were analyzed at 1, 3, 12, 24, 48, and 168 h postinjection using liquid chromatography coupled with mass spectrometry (LC-MS). The highest concentration of MCs (MC-RR + MC-LR) was found in blood, 2–270 ng/g dry weight (DW), followed by heart (3–100 ng/g DW) and kidney (13–88 ng/g DW). MC levels were relatively low in liver, gonad, intestine, spleen, and brain. MC contents in gills, gallbladder, and muscle were below the limit of detection. Significant negative correlation was present between MC-RR concentration in blood and that in kidney, confirming that blood was important in the transportation of MC-RR to kidney for excretion. Rapid accumulation and slow degradation of MCs were observed in gonad, liver, intestine, spleen, and brain. Only 0.07% of injected MCs were detected in liver. The recovery of MCs in liver of crucian carp seemed to be dose dependent.