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AEA administration significantly reduced the nociceptive behavior in both phases of the formalin test (Fig. 1).
This finding is partially in agreement with the observations of Colucci et al. (2008) [59] who showed an increase in the nocifensive behavior in both phases of the formalin test when DMSO was applied subcutaneously in the mouse paw.
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Nociceptive behaviors in both phases of the formalin test were significantly decreased by ritanserin (4 and 8 μl/0.5 μl) and ritanserin had no effect at 2 μl/0.5 μl.
The chimpanzees were observed to probe more during the Control sessions compared to during Baseline sessions (T+ = 0.00, N = 7, P = 0.018), indicating comparably low levels of probing behaviors in both phases.
Importantly, GFP-RabA1d signal intensity exhibited an oscillatory behavior in-phase with tip growth.
AEA induced a significant decrease in the nociceptive behavior during both phases of the formalin test in the animals treated with vehicle; furthermore, AEA abolished NTG-induced hyperalgesia in phase II of formalin test.
AEA induced a significant decrease in the nociceptive behavior during both phases of the formalin test in the animals treated with vehicle, while it abolished NTG-induced hyperalgesia during the phase II.
In agreement with our previous findings [20, 21], NTG administration significantly increased nocifensive behavior in Phase II (hyperalgesic phase) of the orofacial formalin test, when compared to control group (CT) (Fig. 1a).
Twenty-four specimens were constructed with two annealed glass plies and transparent interlayer and were subjected to four point bending tests with the aim to study their structural behavior in both elastic and post-breaking phases.
This paper gives an overview of recent progress in experimental and theoretical studies of diffusion behavior in the phases of the Ti Al system.
Various studies in the literature attempted to study the drug solubilization behavior in different phases generated during lipid digestion using a combination of phase studies coupled with solubility studies 13, 14.
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