Dimethyl Cardamonin from Fruits of Campomanesia reitziana D. Legrand Promotes Gastroprotection and Gastric Healing Effects in Rodents

• Published in: Chemistry & biodiversity Vol. 19; no. 12; pp. e202200727 - n/a
• Main Authors: Cury, Benhur Judah, Boeing, Thaise, Somensi, Lincon Bordignon, Campos, Adriana, Cechinel‐Filho, Valdir, Souza, Priscila, Silva, Luisa Mota
• Format: Journal Article
• Language: English
• Published: Switzerland Wiley Subscription Services, Inc 01.12.2022
• Subjects: Acetic acid; Acidity; Adenocarcinoma; Adenosine Triphosphatases; Animal models; Animals; Anti-Ulcer Agents - chemistry; Anti-Ulcer Agents - pharmacology; Anti-Ulcer Agents - therapeutic use; Cancer; cardamonin; chalcone; Chalcones - pharmacology; Chalcones - therapeutic use; Cytotoxicity; Ethanol; Evaluation; Fibroblasts; Fruit; Fruits; Gastric mucosa; gastric secretion; gastric ulcer; Healing; Humans; Hydrogen; Indomethacin; Inflammation; Mice; Mode of action; Myrtaceae; Nitric oxide; Nitric-oxide synthase; Oxidative stress; Peroxidase; Plant Extracts - chemistry; Plant Extracts - pharmacology; Plant Extracts - therapeutic use; Potassium; Rabbits; Rats; Rats, Wistar; Rodentia; Rodents; Stomach Ulcer - chemically induced; Stomach Ulcer - drug therapy; Stomach Ulcer - pathology; Ulcer - drug therapy; Ulcers; Yohimbine; chalcone; cardamonin; fruits; gastric ulcer; gastric secretion
• ISSN: 1612-1872; 1612-1880
• DOI: 10.1002/cbdv.202200727

Campomanesia reitziana D. Legrand (Myrtaceae) displays antiulcer properties when given to rodents. The major active chemical components of C. reitziana are chalcones, including 4′,6′‐dihydroxy‐2′‐methoxy‐3′,5′‐dimethylchalcone or dimethyl cardamonin (DMC); therefore, we hypothesized that this compound could have antiulcer effects and the present study aimed to evaluate its gastroprotective and gastric healing properties. DMC was isolated from the fruits of C. reitziana, and its gastroprotective effect was evaluated by ethanol and indomethacin‐induced gastric ulcer models in mice (0.1 mg/kg, i.p. and 1 and 3 mg/kg, p.o.). Oxidative stress and inflammatory parameters were analyzed in the gastric tissue. Moreover, its gastric healing effect was evaluated in rats. In addition, the compound's mode of action was evaluated in vivo and in vitro by measuring H+‐K+‐ATPase activity. Finally, the cytotoxic potential of DMC was tested in fibroblasts and human gastric adenocarcinoma cells. The DMC reduced the ethanol‐induced gastric ulcer in mice by 77 %, increased the adhered mucus, and reduced lipoperoxides levels. The block of nonprotein sulfhydryls (NP‐SH) compounds by pretreatment with N‐ethylmaleimide (NEM), the inhibition of nitric oxide synthase with Nω‐nitro‐L‐arginine methyl ester hydrochloride (L‐NAME), or the antagonism of α2 receptor using yohimbine reversed the gastroprotective effects of DMC. Furthermore, DMC reduced the acidity of gastric content in pylorus‐ligated rats but did not change H+, K+‐ATPase (isolated from rabbit) activity in vitro. DMC reduced the lesion area in acetic acid‐induced ulcers and decreased myeloperoxidase activity. DMC did not change the viability of fibroblast cells (L929) but reduced the viability of human gastric adenocarcinoma cells (AGS). The results confirmed that DMC could significantly enhance the gastric healing process and prevent ulcers due to improving protective factors on the gastric mucosa and reducing gastric acid secretion.