Effect of 2,4-Thiazolidinedione on Limousin Cattle Growth and on Muscle and Adipose Tissue Metabolism

Author:

Arévalo-Turrubiarte M.1,González-Dávalos L.2,Yabuta A.3,Garza J. D.1,Dávalos J. L.3,Mora O.12,Shimada A.12

Affiliation:

1. Programa de Posgrado en Ciencias de la Producción y de la Salud Animal, Universidad Nacional Autónoma de México (UNAM), 54714 Mexico City, DF, Mexico

2. Laboratorio de Rumiología y Metabolismo Nutricional (RuMeN), Facultad de Estudios Superiores Cuautitlán (FES Cuautitlán), UNAM, Bulevar B. Quintana 514-D, Colonia Arboledas, 75230 Querétaro, QRO, Mexico

3. Facultad de Medicina Veterinaria y Zootecnia (FMVZ), UNAM and Centro de Enseñanza, Investigación y Extensión en Producción Animal en el Altiplano (CEIEPAA), 76790 Tequisquiapan, QRO, Mexico

Abstract

The main adipogenic transcription factor PPARγpossesses high affinity to 2,4-TZD, a member of the Thiazolidinedione family of insulin-sensitizing compounds used as adipogenic agents. We evaluated 2,4-TZD’s effect on bovine growth and PPAR tissue expression. Seventeen Limousin bulls (18 month-old; 350 kg body weight (BW)) were assigned into 2 treatments: control and 2,4-TZD (8 mg/70 kg BW) and were fed until bulls reached 500 kg BW. They were weighed and their blood was sampled. DNA, RNA, and protein were determined in liver; skeletal muscle; subcutaneous (SC), omental, perirenal adipose tissues (AT) to determine protein synthesis rate and cellular size. Expression of PPAR mRNA was measured in liver and muscle (PPARα, -δ, and -γ) and SC adipose tissue (γ) by real-time PCR. No significant differences were found (P>0.1) in weight gain, days on feed, and carcass quality. Muscle synthesis was greater in controls (P<0.05); cell size was larger with 2,4-TZD (P<0.05). PPARα, -δ, and -γexpressions with 2,4-TZD in liver were lower (P<0.01) than in muscle. No differences were found for PPARγmRNA expression in SCAT. The results suggest the potential use of 2,4-TZD in beef cattle diets, because it improves AT differentiation, liver, and muscle fatty acid oxidation that, therefore, might improve energy efficiency.

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Hindawi Limited

Subject

Pharmacology (medical),Drug Discovery

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