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. Author manuscript; available in PMC: 2018 Sep 16.
Published in final edited form as: Burns. 2006 Jul 11;32(6):755–764. doi: 10.1016/j.burns.2006.01.011

Table 1.

Summary of experimental parameters

Common parameters
Pulse sequence
 12 constant-current pulses
 4 ms duration each
 Field strength of ~150 V/cm in hind limb
 10 s interval between pulses
Injection times
 Therapeutic agent: 10 min post-shock
 Radiotracer: 30 min post-shock
Radiotracer
99mTc pyrophosphate
 Nominal injected activity: 37 ± 7.4 MBq (1.0 ± 0.2 mCi)
Image acquisition
 2 min duration for each image
 New image starting every 2.4 min
 ~3.5 h (88–90 images)
Experimental group namea No. of rats Shocked? (current) Therapeutic agent

Type Amountb (blood concc)

0 A saline 4 No Saline
0 A 17 mg poloxamer-188 3 No Poloxamer-188 17 mg (1 mg/ml)
0.5 A saline 2 Yes (0.5 A) Saline
1.0 A saline 4 Yes (1.0 A) Saline
1.85 A saline 8 Yes (1.85 A) Saline
1.85 A 17 mg poloxamer-188 10 Yes (1.85 A) Poloxamer-188 17 mg (1 mg/ml)
1.85 A 68 mg poloxamer-188 4 Yes (1.85 A) Poloxamer-188 68 mg (4 mg/ml)
1.85 A 17 mg 10 kDa dextran 10 Yes (1.85 A) 10 kDa dextran 17 mg (1 mg/ml)
1.85 A 17 mg 40 kDa dextran 14 Yes (1.85 A) 40 kDa dextran 17 mg (1 mg/ml)
a

Designated by applied current and therapeutic agent.

b

Dissolved in 0.4 ml of saline.

c

Assuming an average blood volume of 17 ml.