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. Author manuscript; available in PMC: 2014 Nov 1.
Published in final edited form as: Obesity (Silver Spring). 2014 Mar 17;22(5):1212–1215. doi: 10.1002/oby.20691

Figure 2.

Figure 2

Plasma concentrations of alloisoleucine in Zucker and DIO rat models or obesity. Plasma alloisoleucine concentrations in (A) lean and obese Zucker rats fed a low fat (chow) diet or (B) lean and obese Sprague-Dawley DIO rats fed a HF diet as described in the Methods and Procedures. The results are mean ± SE, n=9–10, ** p=0.0051, ns indicates not significant. (C) Schematic summarizing previous findings in these two models related to branched chain amino acids. Zucker rats fed even a low fat diet and SD rats fed a high fat diet have increased caloric and BCAA intake and develop obesity associated with elevated BCAAs albeit BCAA elevations are greater in Zucker compared to DIO rats; both models exhibit impairments in adipose tissue BCAA metabolism that include BCKDC (see Results text statements and References 5, 7, 8). The combination of impaired BCKDC activity in fat 5,9 and along with ~50% decreased activity in multiple other peripheral tissues 8 of the obese Zucker rat is posited to explain the observed elevations in alloisoleucine (A). However in the DIO rat loss of BCKDC in fat 7, 9 is compensated for by >50% increase in BCKDC activity in liver as shown by Kadota et al.6. Thus no change in alloisoleucine was observed in DIO rats as S-KMV that is not metabolized in fat can circulate to the liver to be metabolized there.