INT14384
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
These results suggest that P1 and P2 receptors are present in rat duodenum, but their activation is not responsible for the inhibitor effects due to the NANC nerves. | |||||||||||||||
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Final n's for each group were: sham P1 (n = 5), sham P3 (n = 6), sham P5 (n = 5), (total sham= 16); P1 lesion (n = 13); P3 lesion (n = 17); P5 lesion (n = 17).
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Final n's for each group were: sham P1 (n = 5), sham P3 (n = 6), sham P5 (n = 5), (total sham= 16); P1 lesion (n = 13); P3 lesion (n = 17); P5 lesion (n = 17).
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A univariate ANOVA was computed for corpus callosum volume, using Age at Treatment (3 levels; P1, 3, 5) and Treatment (2 levels; Sham, Lesion) as fixed factors (Figure 2). | |||||||||||||||
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In the anaesthetised subjects, only the P1 potential was present. | |||||||||||||||
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The parameters observed were F-VEP latency LP1 (P1 wave response time, ms) and amplitude AP1-N2 (delta between P1 wave trough and N2 wave peak, ? | |||||||||||||||
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Experimental allergic neuritis: cytolysin mRNA expression is upregulated in lymph node cells during convalescence. | |||||||||||||||
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Three patterns of cytokine mRNA expressing MNC in relation to clinical EAN could be distinguished: (i) IL-1beta mRNA expressing cells peaked already on day 3 post immunization (p.i.), and BPM- and P2-reactive TNF-alpha, and BPM-reactive IL-6 mRNA expressing cells were also detected already on day 7 p.i., i.e., before onset of clinical EAN; (ii) BPM- and P2-reactive TNF-alpha peaked together with P2-reactive TNF-beta, IL-6 and IL-12 mRNA expressing cells at height of clinical EAN, consistent with a disease-promoting role for these four cytokines; (iii) high levels of BPM- and P2-reactive IL-10 and cytolysin mRNA expressing cells were observed only during recovery (day 28 p.i.), consistent with a disease down-regulating role of IL-10 and cytolysin. | |||||||||||||||
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Contrary to occludin and claudin-1, the pore-forming TJ protein, claudin-2 [7], was only scarcely detectable in crypts of sham-operated animals, whereas rats from the AP group showed intense staining of claudin-2 both in crypt and surface epithelium (fig 3). | |||||||||||||||
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General Comments
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