TY - JOUR
T1 - Change in kidney damage biomarkers after 13weeks of exposing rats to the complex of Paecilomyces sinclairii and its host Bombyx mori larvae
AU - Jeong, Mihye
AU - Kim, Young Won
AU - Min, Jeong Ran
AU - Kwon, Min
AU - Han, Beom Suk
AU - Kim, Jeong Gyu
AU - Jeong, Sang Hee
N1 - Funding Information:
This work was supported by a research Grant of the Rural Development Administration Korea in 2011.
PY - 2013/9
Y1 - 2013/9
N2 - Complex of Paecilomyces sinclairii and host larvae, Bombyx mori, is a well known health food; however, concerns about nephrotoxicity have been raised. Kidney toxicity was investigated after 13. weeks of administering the complex orally to rats with parameters including blood urea nitrogen (BUN), creatinine, and kidney damage biomarkers, beta-2-microglobulin (β2m), glutathione S-transferase alpha (GST-α), kidney injury molecule 1 (KIM-1), tissue inhibitor of matrix metalloproteinase 1 (TIMP-1), vascular endothelial growth factor (VEGF), calbindin, clusterin, cystatin C, neutrophil gelatinase-associated lipocalin (NGAL), and osteopontin. Dose-dependent kidney cell karyomegaly and tubular hypertrophy were observed, with higher severity in males. There was a dose-dependent increase in KIM-1 and TIMP-1 levels in kidney and urinary KIM-1, cystatin C, β2m, and osteopontin levels. KIM-1 and TIMP-1 increased in male kidneys had not recovered by 2. weeks after stopping exposure. Cystatin C in kidney was significantly lowered in all treatment groups at 13. weeks of administration. All the changes were more noticeable in males. These data indicate that the complex damage renal tubule cells with histopathological lesions and changes in biomarker levels. Kidney and urinary KIM-1 and cystatin C were the most markedly affected and early increased indicators among biomarkers tested, whereas BUN and creatinine were not affected.
AB - Complex of Paecilomyces sinclairii and host larvae, Bombyx mori, is a well known health food; however, concerns about nephrotoxicity have been raised. Kidney toxicity was investigated after 13. weeks of administering the complex orally to rats with parameters including blood urea nitrogen (BUN), creatinine, and kidney damage biomarkers, beta-2-microglobulin (β2m), glutathione S-transferase alpha (GST-α), kidney injury molecule 1 (KIM-1), tissue inhibitor of matrix metalloproteinase 1 (TIMP-1), vascular endothelial growth factor (VEGF), calbindin, clusterin, cystatin C, neutrophil gelatinase-associated lipocalin (NGAL), and osteopontin. Dose-dependent kidney cell karyomegaly and tubular hypertrophy were observed, with higher severity in males. There was a dose-dependent increase in KIM-1 and TIMP-1 levels in kidney and urinary KIM-1, cystatin C, β2m, and osteopontin levels. KIM-1 and TIMP-1 increased in male kidneys had not recovered by 2. weeks after stopping exposure. Cystatin C in kidney was significantly lowered in all treatment groups at 13. weeks of administration. All the changes were more noticeable in males. These data indicate that the complex damage renal tubule cells with histopathological lesions and changes in biomarker levels. Kidney and urinary KIM-1 and cystatin C were the most markedly affected and early increased indicators among biomarkers tested, whereas BUN and creatinine were not affected.
KW - Bombyx mori larvae
KW - Cystatin C
KW - Kidney damage biomarkers
KW - Kidney injury molecule 1
KW - Kidney toxicity
KW - Paecilomyces sinclairii
UR - http://www.scopus.com/inward/record.url?scp=84880129202&partnerID=8YFLogxK
U2 - 10.1016/j.fct.2013.05.041
DO - 10.1016/j.fct.2013.05.041
M3 - Article
C2 - 23747716
AN - SCOPUS:84880129202
SN - 0278-6915
VL - 59
SP - 177
EP - 186
JO - Food and Chemical Toxicology
JF - Food and Chemical Toxicology
ER -