4.7 Article

Analgesic and anti-inflammatory effects and molecular mechanisms of Kadsura heteroclita stems, an anti-arthritic Chinese Tujia ethnomedicinal herb

期刊

JOURNAL OF ETHNOPHARMACOLOGY
卷 238, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2019.111902

关键词

Kadsura heteroclite; Tujia ethnomedicine; Anti-inflammation; Analgesia; Pro-inflammatory cytokines

资金

  1. National Natural Science Foundation of China [81874369, 81703819, 81704065, 81673579]
  2. Hunan Provincial Natural Science Foundation [2017JJ3239, 2018JJ2293]
  3. Hunan Education Department's Science & Research Project [17K069, 17A157]
  4. Hunan Provincial Science & Research Project of Chinese Medicine [201790, 201909]
  5. Hunan Provincial Innovation Project for Outstanding Postgraduate Students [CX2018B476]
  6. Open Foundation Project of Hunan Provincial Key Laboratory of Druggability and Preparation Modification for Chinese Medicine [201701]
  7. 121 Hunan Provincial Training Project for Innovative Talents of Hunan University of Chinese Medicine
  8. National First-class Disciple Construction Project of Chinese Medicine of Hunan University of Chinese Medicine
  9. 2015 Program for Innovative Research Team of Hunan University of Chinese Medicine

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Ethnopharmacological relevance: Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by failure of spontaneous resolution of inflammation. The stem of Kadsura heteroclite (KHS) is a well-known anti-arthritic Tujia ethnomedicinal plant, which named Xuetong in folk, has long been used for the prevention and treatment of rheumatic and arthritic diseases. Aim of the study: The analgesic and anti-inflammatory effects and the potential mechanisms behind such effects of KHS would be investigated by using different animal models. Materials and methods: The abdominal writhing episodes of mice induced by intraperitoneal injection of acetic acid and the tail-flick response induced by radiant heat stimulation were used to evaluate the analgesic effect of KHS. The number of abdominal writhing episodes of mice and the latency of tail-flick in rats were measured and recorded. In acute inflammatory models, the ear edema of mice was induced by applying xylene on the ear surface, while the paw edema of male and female rats was induced by subcutaneous injection of carrageenan into the right hind paws of animals. The carrageenan-induced paw swelling in rats were selected as an anti-acute inflammatory mechanism of KHS. Serum levels of interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), and tumor necrosis factor (TNF-alpha) were measured by ELISA, and protein expression of cyclooxygenase-1 (COX-1), cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) were detected by Western blot. Results: The maximal tolerated single dose of KHS was determined to be 26 g/kg in both sexes of mice. Pharmacological studies showed that KHS at the dose of 200 mg/kg significantly prolonged the reaction time of rats to radiant heat stimulation and suppressed abdominal writhing episodes of mice induced by intraperitoneal injection of acetic acid. KHS at the dose of 200, 400, and 800 mg/kg, showed dose-dependent inhibition of xylene-induced ear swelling in mice. KHS at the dose of 100, 200, 400, and 800 mg/kg demonstrated dose- and time-dependent suppression of paw edema induced by subcutaneous injection of carrageenan in both all rats. Mechanistic studies revealed that the anti-inflammatory effect of KHS was associated with inhibition of the production of pro-inflammatory cytokines IL-beta, and TNF-alpha and effectively decreased the expression of COX and iNOS proteins in the carrageenan-injected rat serum, paw tissues and inflammatory exudates. The positive reference drug, rotundine at a dosage of 100 mg/kg and indomethacin at a dosage of 10 mg/kg were used in both mice and rat models. Conclusion: These results suggested that KHS has significant effects on analgesia and anti-inflammation with decreasing the pro-inflammation cytokines of IL-1A, IL-6, and TNF-alpha and inhibiting the proteins expression of COX-2 and iNOS.

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