Experimental conditions | Drugs in Vitro | n | Rm | gGl |
---|---|---|---|---|
Ω · cm 2 | μS/cm 2 | |||
Exer mdx EDL | 41 | 567 ± 33 | 1480 ± 76 | |
IGF-I 3.3 nM | 28 | 437 ± 203-150 | 1930 ± 803-150 | |
Exer mdx EDL, IGF-1-treated | 50 | 423 ± 17 | 2161 ± 75 | |
IGF-I 3.3 nM | 24 | 477 ± 25 | 1860 ± 77 | |
Exer mdx DIA | 16 | 595 ± 38 | 1344 ± 57 | |
IGF-I 3.3 nM | 12 | 497 ± 30 | 1651 ± 563-150 | |
Exer mdx DIA, IGF-1-treated | 16 | 484 ± 28 | 1760 ± 62 | |
IGF-1 3.3 nM | 12 | 549 ± 65 | 1652 ± 95 |
Each value is the mean ± S.E.M. for the n number of fibers sampled for 2 to 3 preparation. IGF-1 at 3.3 nM has been tested on Rm and gCl of EDL and DIA muscle fibers of both exercised mdx mice untreated (Exer mdx) and chronically treated with IGF-1 at the dose of 50 μg/kg (Exer mdx, IGF-1 treated).
↵3-150 Significantly different with respect to the relative control value in the absence of IGF-1 (p < 0.05 or less). Even if not indicated, according to what described in the text, the values of gCl of IGF-1-treated EDL and DIA muscle fibers were significantly higher with respect to those of untreated exercised counterparts.