Table 3.
PO | n | % MGAs | CV(n) ± SD | Conditions |
---|---|---|---|---|
Intact MGAs, sham-operated,in vivo | ||||
1 d | 16 | 88 | 14 (7) ± 3 | |
5 d | 15 | 87 | 11 (6) ± 4 | |
15 d | 16 | 94 | 15 (6) ± 3 | |
30 d | 20 | 95 | 13 (5) ± 4 | |
Intact MGAs, PEG hydrogel, in vivo | ||||
1 d | 24 | 92 | 11 (7) ± 4 | |
5 d | 24 | 96 | 12 (7) ± 5 | |
15 d | 21 | 81 | 13 (6) ± 3 | |
30 d | 15 | 87 | 14 (5) ± 4 | |
PEG-fused MGAs, in vitro | ||||
0.5–24 hr | 31 | 16 | ||
0.5–24 hr | 17 | 47 | PEG hydrogel | |
PEG-fused MGAs, in vivo | ||||
1 d | 99 | 27 | Anesthetic | |
1 d | 12 | 25 | PEG hydrogel | |
5–15 d | 11 | 27 | PEG hydrogel | |
20 d | 2 | 50 | PEG hydrogel |
PO, Postoperative time. n, Total number of MGAs tested. % MGAs, Number of MGAs tested that conducted an AP through the lesion site, site of sham operation, and/or site of hydrogel application, divided by the total number of MGA preparations tested (n), times 100%. CV(n) ± SD, Conduction velocity (m/sec) and SD of number (n) of MGA APs traveling in a rostral-to-caudal direction through the lesion site (APs are normally conducted rostrally-to-caudally in MGAs in the intact animal). PEG hydrogels were not applied, and earthworms were not anesthetized, unless explicitly stated. p > 0.10 (Student’st test) for any paired set of CVs from sham-operated versus hydrogel-treated MGAs.