ReferenceID 6243

Stephalagine, an aporphinic alkaloid with therapeutic effects in acute gout arthritis in mice

J Ethnopharmacol

Ethnopharmacological relevance: Gout is an inflammatory disease characterized by the accumulation of monosodium urate crystals (MSU) in the joints, leading to severe pain and inflammation. Stephalagine is a Brazilian Sav

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Reference Id
6243
Evidence Id
22833
Core Evidence Id
22833
Source Reference Id
5764
Herb2 Reference Id
HBREF006561
Subject Paper Key
HBIN044790_35427727
Pubmed Id
35427727
Doi
10.1016/j.jep.2022.115291
Paper Title
Stephalagine, an aporphinic alkaloid with therapeutic effects in acute gout arthritis in mice
Paper Abstract
Ethnopharmacological relevance: Gout is an inflammatory disease characterized by the accumulation of monosodium urate crystals (MSU) in the joints, leading to severe pain and inflammation. Stephalagine is a Brazilian Savanna aporphine alkaloid isolated from Annona crassiflora Mart. Fruit peel, that has been popularly used to treat rheumatism and have been described with antinociceptive properties. However, no studies evaluated the possible therapeutic properties of stephalagine in arthritic pain. Aim of the study: To evaluate the possible antinociceptive and anti-inflammatory effects of stephalagine in an acute gout attack in mice. Materials and methods: Adult male wild type C57BL/6/J/UFU mice (20-25 g) were used (process number 018/17). The treated group received stephalagine (1 mg/kg, by gavage) and the vehicle group received saline (10 mL/kg, by gavage), both 1 h before the MSU crystals (100 μg/ankle joint) administration. All groups were analyzed for mechanical allodynia, thermal hyperalgesia, overt pain-like behaviors, and edema development at 2, 4, 6 and 24 h after injections. Synovial fluid and the ankle articulation from the injected joint were collected 4 h after administrations for myeloperoxidase enzyme activity, IL-1β measurement, and histological analysis. Results: Stephalagine had a significant antinociceptive effect on mechanical allodynia, when compared to vehicle group at 2-24 h after intra-articular injection of MSU and 2 h for spontaneous and cold thermal sensitivity. Stephalagine was also able to significantly reduce the articular edema (45 ± 1%), the activity of the myeloperoxidase enzyme (37 ± 6%), and IL-1β levels (43 ± 3%). The histological analysis confirms that stephalagine dramatically reduced the number of infiltrating inflammatory cells (75 ± 6%) in MSU injected animals. Also, stephalagine treatment did not alter the uric acid levels, xanthine oxidase activity, AST and ALT activities, urea and creatinine levels, neither cause any macroscopic changes in the mice's weight, deformations, changes in the coat, or feces. Conclusion: Stephalagine may be an alternative for the management of gout, once it was able to induce antinociceptive and anti-inflammatory effects without causing adverse effects on the evaluated parameters.
Journal
J Ethnopharmacol
Publish Year
2022
Experiment Subject
mouse
Experiment Type
Animal Experiment
Phenotype Related
Pain; Inflammation; Inflammatory Disease; Gout; Rheumatism; Articular Edema; Arthritic Pain
Paper Title Cn
Paper Title En
Stephalagine, an aporphinic alkaloid with therapeutic effects in acute gout arthritis in mice
Bilingual Status
semi_complete