Journal Basic Info

  • Impact Factor: 0.285**
  • H-Index: 6
  • ISSN: 2638-4558
  • DOI: 10.25107/2638-4558
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Allergy & Immunology
  •  Physical Medicine & Rehabilitation
  •  Sports Medicine
  •  Gastric Cancer
  •  Forensic and Legal Medicine
  •  Cancer Clinic
  •  Urology Cases
  •  Sleep Medicine and Disorders


Citation: Clin Case Rep Int. 2023;7(1):1516.DOI: 10.25107/2638-4558.1516

Hepatotoxicity of Microcystin-LR in Wistar Rats

Abeysiri HASN, Wanigasuriya JKP, Suresh TS, Beneragama DH and Manage PM

Department of Zoology, Centre for Water Quality and Algae Research, University of Sri Jayewardenepura, Sri Lanka
University of Sri Jayewardenepura, Sri Lanka
Department of Medicine, Centre for Kidney Research, University of Sri Jayewardenepura, Sri Lanka
Department of Biochemistry, University of Sri Jayewardenepura, Sri Lanka
Department of Pathology, University of Sri Jayewardenepura, Sri Lanka

*Correspondance to: Manage PM 

 PDF  Full Text Research Article | Open Access


Microcystins produced by cyanobacteria have been identified as potent hepato and neurotoxicants to human and livestock. The present study was aimed to determine the possible hepatotoxic effects of MC-LR on mammals using male Wistar rats as an animal model. Thirty-five rats were divided into five groups (n=7 in each). Test groups were orally treated with different doses of MCLR (0.105 μg/kg, 0.070 μg/kg and 0.035 μg/kg). Well water contaminated with MC-LR (0.091 μg/ kg) was given to the environmental exposure group and distilled water was administered to the control group. Body weight was measured once a week. The total duration of exposure of the rats was 90 days. Blood samples were collected at 0, 7, 14, 28, 42, 60, 90 days. Serum concentrations of Aspartate Amino Transferase (AST) and Aspartate Alanine Transferase (ALT) were analyzed from each blood sample. At the end of the experimental period, liver samples were collected for histological examination following accepted protocols. The mean bodyweight of the rats in treated groups of rats gradually increased until the twelfth week and decreased thereafter. A significant decrease in body weight of rats with MC-LR exposure was seen at 13 and 14 weeks, compared to the control group (p=0.000). The absolute and relative weights of livers of the treated groups were significantly lower than the control group (p<0.05). The highest serum AST and ALT levels were observed in rats that were given MC-LR at the dose of 0.105 μg/kg. The hepatocytes showed mild changes including sinusoidal congestion and vascular congestion with lobular inflammation, focal hemorrhages and marked microvesicular steatosis in 0.105 μg/kg group. Mild lobular inflammation, focal hemorrhage, perivenular inflammation, prominent Kupffer cells and focal microvesicular steatosis were observed in 0.091 μg/kg group. Mild lobular inflammation was seen in the group given the dose of 0.070 μg/kg. In conclusion, this study demonstrated that long-term exposure to MC-LR can cause hepatotoxicity in Wistar rats.


Microcystin-LR (MC-LR); Wistar Rats; AST; ALT; Histopathology

Cite the Article:

Abeysiri HASN, Wanigasuriya JKP, Suresh TS, Beneragama DH, Manage PM. Hepatotoxicity of Microcystin-LR in Wistar Rats. Clin Case Rep Int. 2023; 7: 1516.

Search Our Journal

Journal Indexed In

Articles with Grants

Troubleshooting; Split Lung Block for an Ex Vivo Perfusion
 Abstract  PDF  Full Text
Transient ST-Segment Elevation in the Context of MINOCA: A Case Report
 Abstract  PDF  Full Text
View More...