D-Tetramethrin
D-Tetramethrin is a type I synthetic pyrethroid insecticide and hepatotoxicity inducer. D-Tetramethrin induces oxidative stress in the liver of zebrafish. D-Tetramethrin induces Apoptosis and inflammatory responses. D-Tetramethrin causes severe liver damage in zebrafish. D-Tetramethrin can be used in studies related to hepatotoxicity.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 1166-46-7
- 分子式: C19H25NO4
- 分子量:331.41
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
製品説明
体内実験
D-Tetramethrin (0.1-0.15 mg/L; 28 days) induces dose-dependent hepatotoxicity in adult zebrafish, with effects including hepatic histopathological damage, lipid and glucose metabolic disorders, and altered activities of metabolic enzymes[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Animal Model:Transgenic Tg(fabp10a: DsRed); wild-type AB (3 days post-fertilization)[1]
-
Dosage:0.5 mg/L; 1 mg/L; 1.5 mg/L
-
Administration:waterborne exposure; daily;
-
Result:Reduced liver fluorescence area by 10.38% (0.5 mg/L), 7.62% (1 mg/L), and 13.75% (1.5 mg/L) relative to controls.
Increased yolk area by 22.63% (0.5 mg/L), 23.61% (1 mg/L), and 41.32% (1.5 mg/L) relative to controls.
Induced nuclear deformities, loose irregular intercellular gaps, vacuoles, cytoplasmic loss, and nuclear distortion in hepatocytes.
Increased lipid accumulation in a concentration-dependent manner.
Elevated total cholesterol (TC) and total triglycerides (TG) levels significantly across all doses.
Increased alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities significantly relative to controls.
Increased reactive oxygen species (ROS) levels in a concentration-dependent manner.
Elevated catalase (CAT) activity significantly across all doses.
Elevated malondialdehyde (MDA) content significantly across all doses.
Reduced superoxide dismutase (SOD) activity significantly at 1 mg/L and 1.5 mg/L.
Increased expression of apoptosis-related genes (casp-3, casp-6, casp-9, Bax, P53) significantly, while decreased Bcl-2 expression significantly.
Increased Bax/Bcl-2 ratio significantly.
Increased expression of inflammation-related gene TLR4 significantly, while decreased il-10 expression significantly at 1 mg/L and 1.5 mg/L.
Detected no liver-specific apoptosis via TUNEL staining.
Observed significantly fewer proliferating liver cells via PCNA staining.
Reduced expression of cell cycle-promoting genes (ccne1, ccnd1, cdk6) significantly at 1 mg/L and 1.5 mg/L.
-
Animal Model:wild-type AB[1]
-
Dosage:0.1 mg/L; 0.125 mg/L; 0.15 mg/L
-
Administration:waterborne exposure; daily continuous; 28 days
-
Result:Induced nuclear deformities, loose irregular intercellular gaps, and vacuoles in hepatocytes.
Increased lipid droplet accumulation in liver tissue in a concentration-dependent manner.
Elevated low-density lipoprotein cholesterol (LDL-C) levels significantly across all doses.
Increased isocitrate dehydrogenase (cytoplasmic, ICDHc) and glucose-6-phosphate dehydrogenase (G6PDH) activities significantly across all doses.
Increased lactate dehydrogenase (LDH) activity significantly at 0.1 mg/L, while reduced it significantly at 0.125 mg/L and 0.15 mg/L.
Reduced glycogen content significantly.
化学情報
-
CAS 番号 1166-46-7
-
分子量 331.41
-
分子式 C19H25NO4
-
SMILES
C(=C(C)C)[C@@H]1[C@@H](C(OCN2C(=O)C3=C(C2=O)CCCC3)=O)C1(C)C
-
輸送条件
Room temperature in continental US; may vary elsewhere.
-
保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)