TABLE 1.
Effect of AMP-DNM on ceramide and glycosphingolipids in 3T3-L1 adipocytes
| Sphingolipid (pmol/well) | Ceramide | GM3 | GM2 |
|---|---|---|---|
| Without insulin | |||
| No addition | 957 ± 71 | 2,192 ± 144 | 335 ± 21 |
| With TNF | 1,328 ± 95 | 3,265 ± 225 | 442 ± 20 |
| With AMP-DNM | 970 ± 57 | 1,063 ± 65 | 170 ± 12 |
| With TNF + AMP-DNM | 1,241 ± 88 | 2,205 ± 138 | 267 ± 18 |
| With insulin | |||
| No addition | 955 ± 56 | 2,451 ± 184 | 382 ± 26 |
| With TNF | 1,492 ± 92 | 4,288 ± 321 | 619 ± 36 |
| With AMP-DNM | 1,096 ± 56 | 1,074 ± 87 | 175 ± 10 |
| With TNF + AMP-DNM | 1,241 ± 99 | 1,988 ± 169 | 267 ± 97 |
Data are means ± SE. Serum-starved 3T3-L1 adipocytes were treated with either vehicle/control, AMP-DNM (10 μmol/l), and/or TNF-α (0.6 nmol/l) for 24 h prior to stimulation with or without insulin (100 nmol/l for 5 min). Sphingolipid content was determined by HPLC-based procedures as described in research design and methods. Values represent means of four wells. Similar results were obtained in two independent experiments.