4.6 Article

Effects of subchronic exposure to waterborne cadmium on H-P-I axis hormones and related genes in rare minnows (Gobiocypris rarus)

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cbpc.2017.07.002

Keywords

H-P-I axis; Glucocorticoid receptor; FKBP5; Hsp9OAA; Hsp90AB; Glccil

Funding

  1. Major Programme of Science and Technology Commission Foundation of Chongqing [cstc2014yykfc80001]

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The H (hypothalamic)-P (pituitary)-I (interrenal) axis is critical in the stress response and other activities of fish. To further investigate cadmium (Cd) toxicity on the H-P-I axis and to identify its potential regulatory genes in fish, the adult female rare minnows (Gobiocypris rarus) were exposed to subchronic (5 weeks) levels of water-borne Cd in the present study. This kind of treatment caused dose-dependent decline in fish growth, with significance in the high dose group (100 mu g/L). Correspondingly, low dose (5-50 mu g/L) waterborne Cd disrupted the endocrine system of H-P-I axis just at the secretion level, while high dose Cd disrupted both the secretion and synthesis of cortisol and its downstream signals in rare minnows, revealed by the significantly upregulation and positive correlation of corticosteroidogenic genes including MC2R, StAR, CYP11A1, and CYP11B1 in the kidney (including the interrenal tissue) (P < 0.05), and the significant alteration of Glcci1, Hsp90AA and Hsp90AB in the hepatopancreas, gill and intestine as well (P < 0.05). The expression of Glccil was significantly decreased in hepatopancreas, gill and intestine of tested fish following treatment, and its positive correlation with GR (Glucocorticoid receptor) suggested its potential regulation on the cortisol and/or H-P-I axis in fish. The expression of FKBP5 in the intestine was positively and significantly correlated with that of Hsp9OAA (P < 0.05), and the Hsp90AB transcript in the hepatopancreas was positively correlated with that of Hsp9OAA (P < 0.05), which indicated that Hsp9OAA and Hsp90AB were more likely to serve as cofactors of GR and FKBP5 in response to Cd exposure.

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