본문 바로가기
KERD
논문KCI 등재

Ganoderma Lucidum Pharmacopuncture for Teating Ethanol-induced Chronic Gastric Ulcers in Rats

2

조회

0

다운로드

1

인용

0

참고문헌

키워드

주제분류한의학

초록

Objectives: The stomach is a sensitive digestive organ that is susceptible to exogenous pathogens from the diet. In response to such pathogens, the stomach induces oxidative stress, which might be related to the development of both gastric organic disorders such as gastritis, gastric ulcers, and gastric cancer, and functional disorders such as functional dyspepsia. This study was accomplished to investigate the effect of Ganoderma lucidum pharmacopuncture (GLP) on chronic gastric ulcers in rats. Methods: The rats were divided into 4 groups of 8 animals each: the normal, the control, the normal saline (NP) and the GLP groups. In this study, the modified ethanol gastritis model was used. The rats were administrated 56% ethanol orally every other day. The dose of ethanol was 8 g/kg body weight. The normal group received the same amount of normal saline instead of ethanol. The NP and the GLP groups were treated with injection of saline and GLP respectively. The control group received no treatment. Two local acupoints CV12 (中脘) and ST36 (足三里) were used. All laboratory rats underwent treatment for 15 days. On last day, the rats were sacrificed and their stomachs were immediately excised. Results: Ulcers of the gastric mucosa appeared as elongated bands of hemorrhagic lesions parallel to the long axis of the stomach. In the NP and GLP groups, the injuries to the gastric mucosal injuries were not as severe as they were in the control group. Wound healings of the chronic gastric ulcers was promoted by using GLP and significant alterations of the indices in the gastric mucosa were observed. Such protection was demonstrated by gross appearance, histology and immunehistochemistry staining for Bcl-2-associated X (BAX), B-cell lymphoma 2 (Bcl-2) and Transforming growth factor-beta 1 (TGF-β1). Conclusion: These results suggest that GLP at CV12 and ST36 can provide significant protection to the gastric mucosa against an ethanol induced chronic gastric ulcer.

Abstract

Objectives: The stomach is a sensitive digestive organ that is susceptible to exogenous pathogens from the diet. In response to such pathogens, the stomach induces oxidative stress, which might be related to the development of both gastric organic disorders such as gastritis, gastric ulcers, and gastric cancer, and functional disorders such as functional dyspepsia. This study was accomplished to investigate the effect of Ganoderma lucidum pharmacopuncture (GLP) on chronic gastric ulcers in rats. Methods: The rats were divided into 4 groups of 8 animals each: the normal, the control, the normal saline (NP) and the GLP groups. In this study, the modified ethanol gastritis model was used. The rats were administrated 56% ethanol orally every other day. The dose of ethanol was 8 g/kg body weight. The normal group received the same amount of normal saline instead of ethanol. The NP and the GLP groups were treated with injection of saline and GLP respectively. The control group received no treatment. Two local acupoints CV12 (中脘) and ST36 (足三里) were used. All laboratory rats underwent treatment for 15 days. On last day, the rats were sacrificed and their stomachs were immediately excised. Results: Ulcers of the gastric mucosa appeared as elongated bands of hemorrhagic lesions parallel to the long axis of the stomach. In the NP and GLP groups, the injuries to the gastric mucosal injuries were not as severe as they were in the control group. Wound healings of the chronic gastric ulcers was promoted by using GLP and significant alterations of the indices in the gastric mucosa were observed. Such protection was demonstrated by gross appearance, histology and immunehistochemistry staining for Bcl-2-associated X (BAX), B-cell lymphoma 2 (Bcl-2) and Transforming growth factor-beta 1 (TGF-β1). Conclusion: These results suggest that GLP at CV12 and ST36 can provide significant protection to the gastric mucosa against an ethanol induced chronic gastric ulcer.

참고문헌 (16)

  1. Nayeb-Hashemi H, "Gastroduodenal mucosal defense", Curr Opin Gastroenterol, 25(6), pp.537~543 (2009)
  2. Palileo C, "Gastrointestinal defense mechanisms", Curr Opin Gastroenterol, 27(6), pp.543~548 (2011)
  3. Holle GE, "Pathophysiology and modern treatment of ulcer disease", Int J Mol Med, 25(4), pp.483~491 (2010)
  4. Naito Y, "Molecular and cellular mechanisms involved in helicobacter pylori-induced inflammation and oxidative stress", Free Radic Biol Med, 33(3), pp.323~336 (2002)
  5. Repetto MG, "Bioactivity of sesquiterpenes: compounds that protect from alcohol-induced gastric mucosal lesions and oxidative damage", Mini Rev Med Chem, 10(7), pp.615~623 (2010)
  6. Anand BS, "Ulcer and gastritis", Endoscopy, 31(2), pp.215~225 (1999)
  7. Zayachkivska OS, "Influence of plant-originated gastroproteciive and antiulcer substances on gastric mucosal repair", Fiziol Zh, 50(6), pp.118~127 (2004)
  8. Sakat SS, "Gastroprotective effect of oxalis corniculata(whole plant)on experimentally induced gastric ulceration in wistar rats", Indian J Pharm Sci, 74(1), pp.48~53 (2012)
  9. Weng CJ, "The in vitro and in vivo experimental evidences disclose the chemopreventive effects of Ganoderma lucidum on cancer invasion and metastasis", Clin Exp Metastasis, 27(5), pp.361~369 (2010)
  10. 김정대, "A Descriptive Statistical Approach to the Korean Pharmacopuncture Therapy", Journal of Acupuncture & Meridian Studies, 3(3), pp.141~149 (2010), 사단법인약침학회
  11. Owu DU, "Effect of gongronema latifolium ethanol leaf extract on gastric acid secretion and cytoprotection in streptozotocin-induced diabetic rats", West Indian Med J, 61(9), pp.853~860 (2012)
  12. Arumugam S, "Evaluation of anti-ulcer activity of Samanea saman(jacq)merr bark on ethanol and stress induced gastric lesions in albino rats", Indian J Pharmacol, 43(5), pp.586~590 (2011)
  13. McCord JM, "The biology and pathology of oxygen radicals", Ann Intern Med, 89(1), pp.122~127 (1978)
  14. Franke A, "Alcohol-related diseases of the esophagus and stomach", Dig Dis, 23(3-4), pp.204~213 (2005)
  15. Westphal D, "Molecular biology of bax and bak activation and action", Biochim Biophys Acta, 1813(4), pp.521~531 (2011)
  16. Polonikov AV, "Analysis of common transforming growth factor beta-1 gene polymorphisms in gastric and duodenal ulcer disease: pilot study", J Gastroenterol Hepatol, 22(4), pp.555~564 (2007)

관련 논문AI추천

이 간행물의 다른 논문 (8건)