Anti-anaphylactic action of nordihydroguaiaretic acid in antigen sensitized guinea pigs

被引:1
|
作者
Bergren, Dale R. [1 ]
Valentine, Jimmie L. [2 ]
机构
[1] Creighton Univ, Sch Med, Dept Biomed Sci, 2500 Calif Plaza, Omaha, NE 68178 USA
[2] Univ Arkansas Med Sci, Sect Pediat Clin Pharmacol & Toxicol, Little Rock, AR 72205 USA
关键词
Nordihydroguaiaretic acid; Antigen; Airway responsiveness; Leukotrienes; Plethysmography; Guinea pigs; INDUCED BRONCHOSPASM; SRS-A; LIPOXYGENASE INHIBITORS; INDUCED CONTRACTION; BRONCHOCONSTRICTION; 5-LIPOXYGENASE; CONDUCTANCE; ANTAGONISTS; CHALLENGE; EXPOSURE;
D O I
10.1016/j.resp.2016.09.003
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Therapeutic natural products and medicinal herbs has gained popularity. The anti-antigenic action of the plant alkaloid nordihydroguaiaretic acid (NDGA) was studied in ovalbumin (OA)-sensitized guinea pigs. In one series of experiments conscious, non-sedated guinea pigs were challenged With OA aerosol. Specific airway resistance (SRAW) was monitored using a two-chambered whole-body plethysmograph. OA aerosol increased SRAW above that produced by vehicle administration. Prior NDGA administration by a 1 min 0.9% aerosol (w/vol) attenuated the increase in SRAW resulting from OA challenge. In the anesthetized guinea pig pretreated with indomethacin, pyrilamine and propranolol, intravenous OA injection increased intra-tracheal pressure above vehicle injection. Intravenous NDGA administration (5 mg/kg) reduced the intra-tracheal pressure increases. In a third series of experiments plasma leukotriene C-4 was measured by radio-immunoassay in 3 groups challenged with OA aerosol: vehicle-treated OA-sensitized, OA-sensitized receiving NDGA and vehicle treated guinea pigs. NDGA pretreatment reduced plasma LTC4 in response to OA challenge in OA sensitized guinea pigs. This study demonstrates that NDGA is an effective antigenic agent when given by aerosol or intravenous injection in either conscious or anesthetized guinea pigs, respectively. The mechanism of action of NDGA is presumed primarily be due to the blockage of 5-lipoxygenase and therefore the synthesis of leukotrienes. (C) 2016 Elsevier B.V. All rights reserved.
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页码:26 / 31
页数:6
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