Abstract

The effects of microcystin-RR (MC-RR) on water metabolism were studied on Sprague–Dawley (SD) rats and KunMing (KM) mice. In the single dose toxicity test, polydipsia, polyuria, hematuria and proteinuria were found in group of rats receiving a MC-RR dose of 574.7 μg/kg, and could be relieved by dexamethasone (DXM). Gradient damage was observed in kidney and liver in rats with gradient MC-RR doses of 574.7, 287.3, and 143.7 μg/kg. No significant water metabolic changes or kidney injuries were observed in mice treated with MC-RR doses of 210.0, 105.0, and 52.5 μg/kg. In the continuous exposure test, in which mice were administrated with 140.0, 70.0, and 35.0 μg/kg MC-RR for 28 days, mice in the 140.0 μg/kg group presented increasing polydipsia, polyuria, and liver damage. However, no anatomic or histological changes, including related serological and urinary indices, were found in the kidney. In summary, abnormal water metabolism can be induced by MC-RR in rats through kidney injury in single dose exposure; the kidney of SD rats is more sensitive to MC-RR than that of KM mouse; and polydipsia and polyuria in mice exposed to MC-RR for 28 days occurred but could not be attributed to kidney damage.

Highlights

  • Dawley (SD) rats and KunMing (KM) mice

  • Possible abnormal water metabolism induced by microcystinRR in Sprague– Dawley (SD) rats and KM mice was explored and compared

  • The results show that rats administered MC-RR intraperitoneally at a dose of 574.7 μg/kg (3/4 LD50 dose) exhibited polydipsia and polyuria with gross hematuria, urinary microalbumin and protein, and histopathologic kidney changes within 24 h

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Summary

Introduction

Dawley (SD) rats and KunMing (KM) mice. In the single dose toxicity test, polydipsia, polyuria, hematuria and proteinuria were found in group of rats receiving a MC-RR dose of 574.7 μg/kg, and could be relieved by dexamethasone (DXM). Abnormal water metabolism can be induced by MC-RR in rats through kidney injury in single dose exposure; the kidney of SD rats is more sensitive to MC-RR than that of KM mouse; and polydipsia and polyuria in mice exposed to MC-RR for 28 days occurred but could not be attributed to kidney damage. MCs are specific hepatotoxic agents capable of causing acute liver damage in wild and domestic animals exposed to high doses and play a role in tumor promotion in long-term tested animals exposed to lower doses of these toxins [7,8,9,10,11]. Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations

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