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In contrast, there was a tendency toward an increase in vRBC following injection of 20 ml normal saline (P 0.0512).
Hypertonic saline caused significantly higher VAS scores and more extended pain referral than isotonic saline (P < 0.001).
There was no significant change in CPP post-bolus (mannitol p = 0.8 and hypertonic saline p = 0.4).
There was also a tendency toward a difference in the time course of changes in vRBC following injection of iobitridol compared to normal saline (P 0.0607).
Mice treated with χ4550pIL2 or χ4550 had fewer liver tumors and increased populations of hepatic and circulating NK1.1+CD3− lymphocytes compared to mice treated with saline (P < 0.01).
These revealed that TENS maintained its analgesic properties following the injection of saline (p < .001) and the injection of a low dose of naloxone (p < .05).05
PPTs at the injection site and lateral to S2 were significantly reduced after hypertonic saline compared with baseline and isotonic saline (P < 0.002).
IL-1β immunoreactivity was significantly decreased in the repeated treatment KYNA group compared to control groups treated with saline (p < 0.001).
There was no significant difference for T/L (B/A) between the groups receiving 1 mg of AGuIX and normal saline (p = 0.83, independent sample test) (Fig. 5).
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Middle panel Brain PO2 decreased from baseline following hemodilution with both HES and saline (*p < 0.001 vs. baseline).
28.3 ± 1.6 27.8 ± 2.0 3.9 ± 1.1*§ 5.5 ± 1.7°^ * P < 0.01 vs. the corresponding saline/saline ° P < 0.01 vs. the corresponding PTX/saline §P < 0.01 vs. Saline/Indomethacin or saline/prochlorperazine or saline/caffeine or saline/sumatriptan ^ P < 0.01 vs. PTX/indomethacin or PTX/prochlorperazine or PTX/caffeine or PTX/sumatriptan ANOVA.
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