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. Author manuscript; available in PMC: 2020 Nov 22.
Published in final edited form as: Cell Rep. 2020 Nov 10;33(6):108374. doi: 10.1016/j.celrep.2020.108374

Figure 1. Skeletal-Muscle-Specific CPT2-Deficient Mice Accumulate LCACs.

Figure 1.

(A) mRNA and protein expression of Cpt2 in skeletal muscle of Cpt2Sk+/+ and Cpt2Sk−/− mice (n = 6).

(B–E) Complete and incomplete oxidation of 14C-palmitate, 14C-octanoate, and 14C-pyruvate in skeletal muscle homogenates of Cpt2Sk+/+ and Cpt2Sk−/− mice (n = 3).

(F) Acylcarnitine quantification in TA muscle and plasma of Cpt2Sk+/+ and Cpt2Sk−/− female mice (n = 6).

(G and H) Ion intensity per microgram of protein of LCACs and of medium- and short-chain ACs in skeletal muscle of Cpt2Sk+/+ and Cpt2Sk−/− female mice, 24 weeks of age (n = 6).

(I and J) Ion intensity per microliter of plasma of LCACs and of medium- and short-chain ACs in plasma of Cpt2Sk+/+ and Cpt2Sk−/− female mice, 24 weeks of age (n = 6).

(K) Body weight and length of Cpt2Sk+/+ and Cpt2Sk−/− male mice, 12 weeks of age (n = 7–12).

(L) Spontaneous, home-cage locomotor activity during light and dark cycles of male mice, 12 weeks of age (average of 2 recording days, n = 8).

(M) Voluntary wheel activity during light and dark cycles of male mice, 12 weeks of age (average of 2 recording days, n = 8).

Data are presented as mean ± SEM. *p < 0.05 determined by Student’s t test. See also Figure S1.