Serum TNF-alpha levels: potential use to indicate osteoarthritis progression in a mechanically induced model

Serum TNF-alpha levels: potential use to indicate osteoarthritis progression in a mechanically induced model

  • نوع فایل : کتاب
  • زبان : انگلیسی
  • مؤلف : Erdem Aktas Ertugrul Sener Ozlem Zengin Pinar Uyar Gocun Mehmet Ali Deveci
  • چاپ و سال / کشور: 2011

Description

To investigate plasma tumor necrosis factoralpha (TNF-a) levels as an indicator to reflect the magnitude of the destructive inflammatory phase and articular cartilage damage after a knee trauma. Eighteen mature Wistar Albino male rats were divided into two groups equal in number. Nine animals underwent anterior cruciate ligament transection (ACLT) of the right knees, while nine animals had a sham procedure. All animals were killed at the end of 8 weeks; serum TNF-a levels were analyzed with enzyme linked-immunosorbent assay, and the osteoarthritic changes of articular cartilage were evaluated by a histopathological method using OARSI (Osteoarthritis Research Society International) osteoarthritis cartilage histopathology assessment system score. Serum TNF-a levels and OARSI scores showed significant difference between two groups. Despite 8 weeks after the initial trauma, ACLT group still demonstrated elevated levels of plasma TNF-a indicating the ongoing inflammatory phase. Serum TNF-a levels were also found to be correlated with the OARSI osteoarthritis cartilage histopathology assessment system scores. Post-traumatic local TNF-a overproduction as a proinflammatory cytokine is known to have a major role in cartilage matrix degradation. In this study, elevated plasma TNF-a levels were considered as the consequence of the early local inflammatory response to altered knee biomechanics. Degree of articular cartilage damage found to be consistent with plasma TNF-a levels suggest that monitoring plasma TNF-a levels may be a simple and reliable method to reflect the magnitude of destruction during the ongoing inflammatory phase of OA.
Eur J Orthop Surg Traumatol DOI 10.1007/s00590-011-0803-0 Received: 29 January 2011 / Accepted: 22 March 2011
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