Abstract:
OBJECTIVE To study anti-inflammatory effect of the metabolites of endophytes isolated from
Glycyrrhiza uralensis in vivo and
in vitro.
METHODS RAW264.7 cells were inoculated onto a 96-well plate. The model group was added with 1 mg·L
-1 LPS for culture, and each test drug group was added with
Glycyrrhiza water extracts or the fermentation products of endophytes (10, 20, 40 mg·L
-1) for 2 h of treatment, then LPS (1 mg·L
-1) was added for stimulation. The content of nitric oxide (NO), Interleukin-1β (IL-1β) and Prostaglandin E
2 (PGE
2) were measured. Ninety Wistar rats were randomly divided into 9 groups, and each group was given the corresponding drug by gavage administration once per day for 5 d. Except the blank group, the other groups were intravenously injected with LPS (1 mg·kg
-1) to establish an acute pneumonia model, while the blank group was injected with the same volume of normal saline. After 6 h, blood was collected from rat femoral artery to detect peripheral white blood cell counts and the contents of serum TNF-α, IL-6 and IL-10.
RESULTS Compared with LPS model group, when the mass concentration was maintained at 40 mg·L
-1, the contents of NO, PGE
2 and IL-1β were significantly reduced in extractum
Glycyrrhiza group and endophytes fermentation products groups(JTZB006, JTZB018, JTZB059, JTZB060, JTZB063)(
P<0.05 or
P<0.01). The contents of PGE
2 in JTZB006, JTZB060 were significantly lower than those of extractum
Glycyrrhiza group at 40 mg·L
-1. Compared with model group, the white blood cell counts and the contents of TNF-α and IL-6 were significantly reduced in positive control group,
Glycyrrhiza water decoction group, 3 groups of the fermentation products of endophytes. The contents of IL-10 in JTZB006, JTZB060 and JTZB063 significantly higher than those of
Glycyrrhiza water decoction group in rat serum (
P<0.05 or
P<0.01).
CONCLUSION JTZB006, JTZB060 and JTZB063 have anti-inflammatory effects in LPS induced inflammatory model.