{"title":"Pulmonary Protective and Vasodilator Effects of a StandardizedPanax GinsengPreparation Following Artificial Gastric Digestion","authors":"S. Rimar , M. Lee-Mengel , C.N. Gillis","doi":"10.1006/pulp.1996.0025","DOIUrl":null,"url":null,"abstract":"<div><p>We have previously demonstrated that purified ginsenosides produce pulmonary vasodilation and prevent effects of free radical injury on the lung. We examined the effect of artificially digested standardized ginseng preparation G115 in perfused rabbit lungs. G115 was incubated in artificial gastric juice (0.03 M NaCl+0.08 M HCl) 37°C for 1 h, and artificial intestinal juice (0.05 M KH<sub>2</sub>PO<sub>4</sub>+0.02 M NaOH) 37°C for 5 h, neutralized with NaOH and lyophilized. Pulmonary vasoconstriction was induced with U46619, and cumulative additions of G115 in undigested, gastric digested and gastric and intestinal digested forms were made to the perfusate. In separate experiments, oxygen free radical injury by electrolysis was produced in the presence of G115 in the perfusate and ACh-induced vasodilation assessed before and after injury. Undigested, gastric digested and combined gastric and intestinal digested G115 significantly dilated lungs (44%, undigested; 26%, gastric digested; 45%, gastric and intestinal digested). In addition, both undigested (−27±5% vs. −24±5%) as well as gastric and intestinal digested G115 (−23±3% vs. −16±2%) preserved ACh-induced vasodilation following injury. Artificially digested G115 is a pulmonary vasodilator which protects against free radical injury, suggesting that oral G115 has the same effects.</p></div>","PeriodicalId":74618,"journal":{"name":"Pulmonary pharmacology","volume":"9 4","pages":"Pages 205-209"},"PeriodicalIF":0.0000,"publicationDate":"1996-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/pulp.1996.0025","citationCount":"31","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pulmonary pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0952060096900253","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 31
Abstract
We have previously demonstrated that purified ginsenosides produce pulmonary vasodilation and prevent effects of free radical injury on the lung. We examined the effect of artificially digested standardized ginseng preparation G115 in perfused rabbit lungs. G115 was incubated in artificial gastric juice (0.03 M NaCl+0.08 M HCl) 37°C for 1 h, and artificial intestinal juice (0.05 M KH2PO4+0.02 M NaOH) 37°C for 5 h, neutralized with NaOH and lyophilized. Pulmonary vasoconstriction was induced with U46619, and cumulative additions of G115 in undigested, gastric digested and gastric and intestinal digested forms were made to the perfusate. In separate experiments, oxygen free radical injury by electrolysis was produced in the presence of G115 in the perfusate and ACh-induced vasodilation assessed before and after injury. Undigested, gastric digested and combined gastric and intestinal digested G115 significantly dilated lungs (44%, undigested; 26%, gastric digested; 45%, gastric and intestinal digested). In addition, both undigested (−27±5% vs. −24±5%) as well as gastric and intestinal digested G115 (−23±3% vs. −16±2%) preserved ACh-induced vasodilation following injury. Artificially digested G115 is a pulmonary vasodilator which protects against free radical injury, suggesting that oral G115 has the same effects.
我们以前已经证明,纯化人参皂苷产生肺血管舒张和防止自由基损伤对肺的影响。我们观察了人工消化标准人参制剂G115对兔肺灌注的影响。将G115在37℃的人工胃液(0.03 M NaCl+0.08 M HCl)和37℃的人工肠液(0.05 M KH2PO4+0.02 M NaOH)中孵育1 h,用NaOH中和并冻干。U46619诱导肺血管收缩,使未消化、胃消化和胃肠消化形式的G115累积添加到灌注液中。在单独的实验中,在灌注液中存在G115的情况下产生电解氧自由基损伤,并在损伤前后评估ach诱导的血管舒张。未消化、胃消化和胃肠联合消化的G115肺明显扩张(44%,未消化;26%,胃消化;45%,肠胃消化)。此外,未消化的(- 27±5% vs - 24±5%)和胃肠道消化的G115(- 23±3% vs - 16±2%)均保留了损伤后乙酰氨基酚诱导的血管舒张。人工消化的G115是一种肺血管扩张剂,可以防止自由基损伤,这表明口服G115具有相同的效果。