“…The toxic mechanism of TCDD is mediated through combining with the cellular Ah-receptor, after a series of synthesis of protein, the most sensitive biochemical response is considered to be the induction of 7-ethoxyresoru"n-O-deethylase (EROD) activity (Poland and Knutson, 1982;Landers and Brunce, 1991;Safe, 1994;Boening, 1998). Thus, the dose}response relationship between EROD activity and TCDD concentration is increasingly attracting attention throughout the world (Van der Weiden et al, 1992;Nosek et al, 1993;Palace et al, 1996;Wu et al, 1996). At present, because of the extreme toxicity and high cost of developing standards, most studies on TCDD toxicity have involved short-term or one-time exposure (Mehrle et al, 1988;Wisk and Cooper, 1990;Spitsbergen et al, 1991;Walker et al, 1994;Cantrell et al, 1996;Henry et al, 1997;Elonen et al, 1998;Hornung et al, 1999).…”