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. Author manuscript; available in PMC: 2017 Oct 24.
Published in final edited form as: Arch Toxicol. 2016 Nov 8;91(5):2245–2261. doi: 10.1007/s00204-016-1885-6

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.