Peer-reviewed veterinary case report
Protective Effects of(Borago) on Cold Restraint Stress-Induced Gastric Ulcers in Rats: A Pilot Study.
- Journal:
- Frontiers in veterinary science
- Year:
- 2020
- Authors:
- Di Cerbo, Alessandro et al.
- Affiliation:
- School of Biosciences and Veterinary Medicine · Italy
- Species:
- rodent
Abstract
Stress is a typical body's natural defense to a generic physical or psychic change. A specific linking mechanism between ulcer onset and psycho-physical stress prolonged exposure has been reported. We decided to investigate the possible effects ofL. (Borago) in preventing physical (stress)-induced gastric ulcers in a rat model. Eighty male Sprague-Dawley rats were randomly divided into 16 groups, pretreated with a control solution, omeprazole (20 mg/kg), Borago methanolic extract (25, 50, 100, 250, and 500 mg/kg), Borago organic extract (50, 100, 250, and 500 mg/kg), Borago aqueous extract (5, 10, 20, 30, and 40 mg/kg), and D(-)-2-Amino-5-phosphonovaleric acid (AP5) (25 mg/kg) and kept in stressful conditions such as water immersion and restraint-induced stress ulcers. The animals were sacrificed and their stomach scored for the severity and the number of gastric ulcers. Methanolic extract (500 mg/kg) significantly reduced both ulcer parameters (< 0.001 and< 0.01, respectively). Aqueous and organic extract significantly decreased severity score at 5 and 10 mg/kg (< 0.01 and< 0.001, respectively), and at 250 and 500 mg/kg (< 0.001), respectively, while gastric ulcers' resulted number significantly reduced only at 10 mg/kg (< 0.05) and at 500 mg/kg (< 0.01), respectively. On the other hand, aqueous extract significantly increased the mucosal gastric content of cAMP (< 0.05) and NR2A and NR2B subunits (< 0.05 and< 0.01, respectively) at 5 mg/kg. Organic extract showed also a significant cytotoxic effect at 500 and 1,000 mg/kg with a 3T3 cell viability reduction of 43.6% (< 0.01) and 92.1% (< 0.001), respectively. Borago aqueous extract at 10 mg/kg could be considered as a potential protective agent against stress-induced ulcers, and it is reasonable to possibly ascribe such protective activity to a modulation of the NR2A and NR2B subunit expression.
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Search related cases →Original publication: https://pubmed.ncbi.nlm.nih.gov/32984407/