Gastroprotective Effects of Curcuma zedoaria in Ethanol-Induced Gastric Ulcers of Experimental Rats

被引:0
作者
Sutardi, L. N. [1 ]
Mustika, A. A. [2 ]
Andriyanto
Handharyani, E. [3 ]
Winarto, A. [4 ]
Rahma, A. [1 ]
Nabilah, A. S. [5 ]
Rahman, F. A. [4 ]
机构
[1] IPB Univ, Sch Vet Med & Biomed Sci, Sub Div Pharm, Bogor 16680, Indonesia
[2] IPB Univ, Sch Vet Med & Biomed Sci, Div Pharmacol & Toxicol, Bogor 16680, Indonesia
[3] IPB Univ, Sch Vet Med & Biomed Sci, Div Pathol, Bogor 16680, Indonesia
[4] IPB Univ, Sch Vet Med & Biomed Sci, Div Anat Histol & Embryol, Bogor 16680, Indonesia
[5] IPB Univ, Sch Vet Med & Biomed Sci, Bogor 16680, Indonesia
关键词
Curcuma zedoaria; Gastritis; White Turmeric; SUPPRESSION; DAMAGE;
D O I
10.14334/jitv.v29i2.3183
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Gastritis is one of the most common health problems of humans in the world. Gastric ulcer is mostly characterized by inflammation of the epithelial cells lining the gastric mucosa. Stomach injury may occur due to excessive secretion of stomach acid, pepsin, Helicobacter pylori, , stress, smoking habit, alcohol consumption, irregular eating pattern, infection, and the use of non-steroidal anti-inflammatory drugs. This study aimed to explore the gastroprotective effects of Curcuma zedoaria infusion (CZI) on HCl/ethanol-induced gastric mucosal damage in rats. A total of 16 Sprague Dawley rats were randomly divided into 4 groups: negative control (without treatment), positive control (treated with omeprazole), P1 (CZI 30%), and P2 (CZI 60%). Several endpoints were evaluated, including gastric mucosal lesions, cellular degeneration, intracellular damage, and pH value. The gastric mucosal injury and ulcer score were determined by evaluating the inflamed gastric mucosa and by histopathological examination. After the treatment animal with CZI significantly (P<0.05) decreased the ulcer index by preventing gastric mucosal lesions, erosion, and cellular degeneration, and the value of pH value was increased (P<0.05). These results demonstrate that CZI has significant gastroprotective properties which support its use in traditional medicine.
引用
收藏
页码:97 / 102
页数:6
相关论文
共 26 条
  • [1] Afify Abd EL-Moneim M. R., 2012, Advances in Food Sciences, V34, P145
  • [2] Olive (Olea europaea) leaf methanolic extract prevents HCl/ethanol-induced gastritis in rats by attenuating inflammation and augmenting antioxidant enzyme activities
    Al-Quraishy, Saleh
    Othman, Mohamed S.
    Dkhil, Mohamed A.
    Moneim, Ahmed Esmat Abdel
    [J]. BIOMEDICINE & PHARMACOTHERAPY, 2017, 91 : 338 - 349
  • [3] Azam G, 2017, J Pharmacogn Phytochem., V6, P171
  • [4] Ameliorating and protective effects mesalazine on ethanol-induced gastric ulcers in experimental rats
    Beiranvand, Mohammad
    Bahramikia, Seifollah
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2020, 888
  • [5] Bujanda L, 2000, AM J GASTROENTEROL, V95, P3374, DOI 10.1111/j.1572-0241.2000.03347.x
  • [6] Protective effects of β-glucan isolated from highland barley on ethanol-induced gastric damage in rats and its benefits to mice gut conditions
    Chen, Haihong
    Nie, Qixing
    Xie, Min
    Yao, Haoyingye
    Zhang, Ke
    Yin, Junyi
    Nie, Shaoping
    [J]. FOOD RESEARCH INTERNATIONAL, 2019, 122 : 157 - 166
  • [7] Suppression of Growth Arrest and DNA Damage-Inducible 45α Expression Confers Resistance to Sulindac and Indomethacin-Induced Gastric Mucosal Injury
    Chiou, Shiun-Kwei
    Hodges, Amy
    Hoa, Neil
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2010, 334 (03) : 693 - 702
  • [8] Coșkun O., 2004, European Journal of General Medicine, V1, P37
  • [9] Mechanisms of curcumin-induced gastroprotection against ethanol-induced gastric mucosal lesions
    Czekaj, Renata
    Majka, Jolanta
    Magierowska, Katarzyna
    Sliwowski, Zbigniew
    Magierowski, Marcin
    Pajdo, Robert
    Ptak-Belowska, Agata
    Surmiak, Marcin
    Kwiecien, Slawomir
    Brzozowski, Tomasz
    [J]. JOURNAL OF GASTROENTEROLOGY, 2018, 53 (05) : 618 - 630
  • [10] Gozali K, 2022, Jambura J Heal Sci Res., V4, P648, DOI [10.35971/jjhsr.v4i3.13309, DOI 10.35971/JJHSR.V4I3.13309]