Penissi A B, Rudolph M I, Villar M, Coll R C, Fogal T H, Piezzi R S
Instituto de Histología y Embriología Dr. Mario H. Burgos (IHEM-CONICET), Facultad de Ciencias Médicas, Universidad Nacional de Cuyo, Casilla de Correo 56, (5500) Mendoza, Argentina.
Inflamm Res. 2003 May;52(5):199-205. doi: 10.1007/s000110300072.
DhL, a lactone isolated from Artemisia douglasiana, prevents gastrointestinal damage elicited by necrosis-inducing agents and exhibits antiinflammatory action. This work examines the effect of DhL on compound 48/80-induced histamine and serotonin release in the isolated mouse jejunum, to determine whether DhL inhibits mediator release from mast cells at the enteric level.
Thirty jejuna from male Balb-c mice were used for the studies.
Samples were incubated sequentially in 9 test tubes containing RBS or 10 microg/ml compound 48/80 or 1.6 mmol/l + 10 microg/ml compound 48/80 at 37 degrees C for 90 minutes (10 min per tube).
Histamine and serotonin release studies, quantification of granulated mast cells, and evaluation of mast cell ultrastructure were carried out. Differences between groups were determined using analysis of variance followed by Tukey-Kramer multiple comparisons test.
Compound 48/80 increased histamine and serotonin release by the tissue (141.95 +/- 62.58 pg/mg tissue vs basal 5.45 +/- 1.04, P<0.01 and 20.04 +/- 2.81 vs basal 9.24 +/- 1.56 ng/ mg tissue, P<0.01, respectively), decreased the number of granulated submucosal mast cells (0.077 +/- 0.0035 vs basal 0.14 +/- 0.015, P<0.05), and elicited evident granule ultrastructural changes. These effects were reduced by dehydroleucodine (19.51 +/- 7.88, P<0.01; 12.69 +/- 1, P<0.05 and 0.143 +/- 0.014, P<0.05, respectively).
The lactone inhibits compound 48/80-induced histamine and serotonin release from mast cells in the isolated mouse jejunum.
DhL是从道格拉斯蒿中分离出的一种内酯,可预防由坏死诱导剂引起的胃肠道损伤,并具有抗炎作用。本研究旨在考察DhL对化合物48/80诱导的离体小鼠空肠组胺和5-羟色胺释放的影响,以确定DhL是否在肠道水平抑制肥大细胞释放介质。
选用30段雄性Balb-c小鼠的空肠用于研究。
将样本依次置于9支试管中,在37℃下分别用RBS、10μg/ml化合物48/80或1.6mmol/L + 10μg/ml化合物48/80孵育90分钟(每管10分钟)。
进行组胺和5-羟色胺释放研究、颗粒化肥大细胞定量分析以及肥大细胞超微结构评估。组间差异采用方差分析及Tukey-Kramer多重比较检验确定。
化合物48/80使组织中组胺和5-羟色胺释放增加(分别为141.95±62.58pg/mg组织,而基础值为5.45±1.04,P<0.01;20.04±2.81 vs基础值9.24±1.56ng/mg组织,P<0.01),使黏膜下颗粒化肥大细胞数量减少(0.077±0.0035 vs基础值0.14±0.015,P<0.05),并引起明显的颗粒超微结构变化。脱氢亮氨酸可减轻这些作用(分别为19.51±7.88,P<0.01;12.69±1,P<0.05和0.143±0.014,P<0.05)。
该内酯可抑制化合物48/80诱导的离体小鼠空肠肥大细胞释放组胺和5-羟色胺。