Title : beta-Adrenergic blockade during systemic inflammation: impact on cellular immune functions and survival in a murine model of sepsis.

Pub. Date : 2007 Feb

PMID : 17118511






1 Functional Relationships(s)
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1 RESULTS: Administration of propranolol in septic mice increased the splenocyte apoptosis rate, reduced the proliferative capacity of splenocytes, and modulated cellular cytokine release (IL-6, IFN-gamma). Propranolol interleukin 6 Mus musculus