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No evidence for release of superoxide into the interstitial space was found during reperfusion, although this was observed during electrically stimulated contractile activity of the rat limb muscle.
The investigation and quantification of viral load within the infected host could provide evidence for release of virus and methods of transmission.
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While direct evidence for PACAP release in the SCN is limited, local application of PACAP [66, 82] in-vitro was shown to phase advance SCN neurons during the subjective day via a PAC1 dependent mechanism, but not at night, suggesting a role for PACAP in daytime regulation of the circadian cycle.
Already in 1982, Theoharides et al. [32] found evidence for differential release of MC mediators from the secretory granules.
These results provide genetic evidence for receptor release of these regions of PA as being necessary for the protein rearrangements that accompany anthrax toxin pore formation.
Evidence for the release of exosomes by RPE and localization of αB crystallin within the exosomes was achieved by immunoblot, immunofluorescence, and electron microscopic analyses.
We found evidence for sperm release from the female reproductive tract that specifically affects SR males.
Taken together, we provide evidence for the release of mitochondria during necroptosis.
Evidence for multivesicular release is particularly strong for electrically non-excitable cells [ 6, 7, 12], but recent data indicate that it also occurs in intensely stimulated neurons [ 13].
Evidence for the release of cytokines from native host tissue is found in the presence of a persistent inflammatory response, mediated by T helper 1 (Th1) cells [ 55].
However, we did not find evidence for the release of free PUFAs out of N. limnetica after cell damage (G. Pohnert, unpubl. data).
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