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. 1999 Apr 1;19(7):2442–2454. doi: 10.1523/JNEUROSCI.19-07-02442.1999

Table 3.

Conduction of MGA APs in intact or PEG-fused MGAs versus postoperative time

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.