The present study was performed to determine whether genistein could inhibi
t in vivo LPS-induced alveolar macrophage TNF alpha production and thus red
uce the alveolar neutrophil. influx following LPS. In vitro incubation with
genistein completely inhibited LPS-induced TNF alpha production by alveola
r macrophages (AM) from BALB/c mice. Subsequently mice were pretreated with
intraperitoneal genistein or vehicle, then received nasal LPS to induce an
alveolitis. Genistein was then administered every eight hours for five day
s following LPS. At 24 hours after LPS, the bronchoalveolar lavage (BAL) TN
F alpha and ex vivo TNF alpha production from AM, were lower in the geniste
in treated animals. As well, total BAL white blood cell (WBC) count was red
uced in the genistein as compared to the vehicle-only group. The percent ne
utrophils and the resolution of neutrophils were similar between genistein
and vehicle groups. Therefore, genistein was able to decrease AM TNF alpha
production, and was associated with a decrease in BAL WBC count post-LPS.