Soft tissue injuries are common, often debilitating, disorders. They most frequently affect young healthy individuals and are a leading cause of time lost from the work place and the sporting field. The long term objectives of this project are to improve and enhance the management of these injuries. Our previous in vitro investigations indicate that oxygen free radicals can modulate fibroblast proliferation and may provide a rapid, sensitive mechanism for inter-cellular communication, a mechanism that can be readily modulated by pharmacological means. The free radical milieu of healing tendon will be determined by measuring the potential for xanthine oxidase mediated free radical generation, lipid peroxidation, NADPH oxidase activity, and the expression of antioxidant enzymes. A series of in vitro experiments are planned to delineate the hormetic effects of oxygen free radicals on fibroblasts cultured from both human and rat Achilles tendon and skin.
We aim to gain a better understanding of the mechanisms whereby superoxide radicals are released in fibroblasts, how free radicals stimulate fibroblast proliferation and chemotaxis and the role of """"""""endogenous"""""""" free radicals in fibroblast proliferation and chemotaxis. Sensitive, reproducible methods will be developed to test the functional performance and the mechanical properties of injured rat Achilles tendons. These methods, along with biochemical and morphological assessments, will be utilized to test agents which modify the free radical environment of healing Achilles tendons in vivo. Tumor necrosis factor alpha (TNF-alpha), an agent which both increases free radical release and enhances the cells' defence against radical damage, has already shown promise as an agent which may enhance tendon healing. We anticipate that this project will provide new and clinically relevant information on the mechanisms of tendon healing and act as a forerunner for the clinical testing of agents that will enhance soft tissue healing.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
1R29AR042729-01
Application #
3457805
Study Section
Orthopedics and Musculoskeletal Study Section (ORTH)
Project Start
1993-08-10
Project End
1998-07-31
Budget Start
1993-08-10
Budget End
1994-07-31
Support Year
1
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Hospital for Special Surgery
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10021
Murrell, George A C (2007) Using nitric oxide to treat tendinopathy. Br J Sports Med 41:227-31
Wang, M X; Murrell, D F; Szabo, C et al. (2001) Nitric oxide in skeletal muscle: inhibition of nitric oxide synthase inhibits walking speed in rats. Nitric Oxide 5:219-32
Murrell, G A; Jang, D; Deng, X H et al. (1998) Effects of exercise on Achilles tendon healing in a rat model. Foot Ankle Int 19:598-603
Jang, D; Murrell, G A (1998) Nitric oxide in arthritis. Free Radic Biol Med 24:1511-9
Murrell, G A; Szabo, C; Hannafin, J A et al. (1997) Modulation of tendon healing by nitric oxide. Inflamm Res 46:19-27
Murrell, G A; Doland, M M; Jang, D et al. (1996) Nitric oxide: an important articular free radical. J Bone Joint Surg Am 78:265-74
Jang, D; Szabo, C; Murrell, G A (1996) S-substituted isothioureas are potent inhibitors of nitric oxide biosynthesis in cartilage. Eur J Pharmacol 312:341-7
Manfield, L; Jang, D; Murrell, G A (1996) Nitric oxide enhances cyclooxygenase activity in articular cartilage. Inflamm Res 45:254-8
Murrell, G A; Jang, D; Williams, R J (1995) Nitric oxide activates metalloprotease enzymes in articular cartilage. Biochem Biophys Res Commun 206:15-21
Murrell, G A; Lilly 3rd, E G; Goldner, R D et al. (1994) Effects of immobilization on Achilles tendon healing in a rat model. J Orthop Res 12:582-91