Table 2. Panx1 glycosylation status after APAP overdosing.
Time point | Treatment | Total Panx1 normalized to 0 hour | Gly0 (%) | Gly1 (%) | Gly2 (%) |
---|---|---|---|---|---|
0 hour | / | 1.00 ± 0.14 | 49.5 ± 1.4 | 13.9 ± 1.9 | 36.6 ± 3.3 |
1 hour | SAL | 1.21 ± 0.10 | 58.6 ± 2.0 | 14.0 ± 1.9 | 27.3 ± 3.0 |
APAP | 0.85 ± 0.10 | 48.8 ± 3.5 | 5.2 ± 1.7*** | 46.0 ± 4.2** | |
6 hours | SAL | 1.18 ± 0.11 | 54.1 ± 1.6 | 10.4 ± 1.3 | 35.6 ± 2.4 |
APAP | 2.08 ± 0.27 | 11.4 ± 5.7**** | 4.0 ± 1.0* | 84.5 ± 6.6**** | |
24 hours | SAL | 1.96 ± 0.19 | 63.0 ± 1.8 | 18.1 ± 1.7 | 18.8 ± 0.7 |
APAP | 3.31 ± 0.20 | 5.7 ± 1.8**** | 3.8 ± 0.3**** | 90.5 ± 1.9**** |
Mice (n = 5) were injected 300 mg/kg APAP or saline (SAL) followed by sampling at different time points (0, 1, 6 and 24 hours). Hepatic protein levels of Panx1 were assessed by immunoblot analysis where Panx1 was detected as 3 signals, representing the non-glycosylated core (Gly0), the high-mannose (Gly1) and the complex glycosylated species (Gly2). Data were expressed as means ± SEM, with *p < 0.05, **p < 0.01, ***p < 0.001 and ****p < 0.0001 compared to vehicle control at indicated time points.