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Interleukin-1 as a pharmacological target in acute brain injury
Interleukin-1 as a pharmacological target in acute brain injury
DOI: 10.1113/EP085135
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- This is an Accepted Article that has been peer-reviewed and approved for publication in the Experimental Physiology, but has yet to undergo copy-editing and proof correction. Please cite this article as an ‘Accepted Article’; doi: 10.1113/EP085135.
Acute
brain injury is one of the leading causes of mortality and disability
worldwide. Despite this, treatments for acute brain injuries are limited
and there remains a massive unmet clinical need. Inflammation has
emerged as a major contributor to non-communicable diseases and there is
now substantial and growing evidence that inflammation, driven by the
cytokine interleukin-1 (IL-1), worsens acute brain injury. IL-1 is
regulated by large multi-molecular complexes called inflammasomes. Here
we discuss the latest research on the regulation of inflammasomes and
IL-1 in the brain, pre-clinical efforts to establish the IL-1 system as a
therapeutic target, and the promise of recent and future clinical
studies of blocking IL-1 action for the treatment of brain injury.
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