Title : 3-Methylcholanthrene Induces Chylous Ascites in TCDD-Inducible Poly-ADP-Ribose Polymerase (Tiparp) Knockout Mice.

Pub. Date : 2019 May 10

PMID : 31083300






6 Functional Relationships(s)
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1 3-Methylcholanthrene Induces Chylous Ascites in TCDD-Inducible Poly-ADP-Ribose Polymerase (Tiparp) Knockout Mice. Methylcholanthrene TCDD-inducible poly(ADP-ribose) polymerase Mus musculus
2 3-Methylcholanthrene Induces Chylous Ascites in TCDD-Inducible Poly-ADP-Ribose Polymerase (Tiparp) Knockout Mice. Methylcholanthrene TCDD-inducible poly(ADP-ribose) polymerase Mus musculus
3 In this study, we treated male Tiparp-/- or wild type (WT) mice with a single injection of 100 mg/kg 3-methylcholanthrene (3MC). Methylcholanthrene TCDD-inducible poly(ADP-ribose) polymerase Mus musculus
4 Consistent with TIPARP"s role as a repressor of AHR signaling, 3MC-treated Tiparp-/- mice exhibited increased hepatic Cyp1a1 and Cyp1b1 levels compared with WT mice. Methylcholanthrene TCDD-inducible poly(ADP-ribose) polymerase Mus musculus
5 Consistent with TIPARP"s role as a repressor of AHR signaling, 3MC-treated Tiparp-/- mice exhibited increased hepatic Cyp1a1 and Cyp1b1 levels compared with WT mice. Methylcholanthrene TCDD-inducible poly(ADP-ribose) polymerase Mus musculus
6 Our study reveals that Tiparp-/- mice have increased sensitivity to 3MC-induced liver toxicity, but unlike with TCDD, lethality is due to chylous ascites rather than wasting syndrome. Methylcholanthrene TCDD-inducible poly(ADP-ribose) polymerase Mus musculus