4.3. Measurement of Serum AST, ALT, BUN, Creatinine, and Triglyceride Levels and Hepatic Triglyceride Levels

GC Geng-Ruei Chang
HL Hsien-Yueh Liu
WY Wei-Cheng Yang
CW Chao-Min Wang
CW Ching-Fen Wu
JL Jen-Wei Lin
WL Wei-Li Lin
YW Yu-Chen Wang
TL Tzu-Chun Lin
HL Huei-Jyuan Liao
PH Po-Hsun Hou
CC Chee-Hong Chan
CL Chuen-Fu Lin
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A Catalyst One Chemistry Analyzer (IDEXX Laboratories, Westbrook, ME, USA) and commercial kits were employed, following the manufacturer instructions, to measure AST, ALT, BUN, triglyceride, and creatinine levels in blood samples. Inter- and intra-analyses had coefficients of variation < 2%. Triton X-100 solution was employed to obtain hepatic triglycerides from homogenized liver samples, as was done in another study [90]. Extract solubilization was then performed; the extracts were twice heated gradually to 90 °C over 5 min and subsequently cooled to room temperature. Insoluble material was removed through centrifugation. Lastly, we obtained the supernatant and employed the Triglyceride Quantification Kit from BioVision (Milpitas, CA, USA) to subject it to colorimetric assay-based triglyceride analysis.

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