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Literature DB >> 3924826

Arachidonic acid facilitates experimental chronic osteomyelitis in rats.

J P Rissing, T B Buxton, J Fisher, R Harris, R K Shockley.

Abstract

Arachidonic acid was used as a facilitating agent in experimental rat Staphylococcus aureus osteomyelitis and compared with the more commonly used agent, sodium morrhuate. The injection of arachidonic acid or sodium morrhuate and S. aureus into rat tibiae caused increased quantitative bacterial bone counts, gross bone pathology, roentgenographic changes, and weight loss. The doses required to produce these changes appeared to be lower for arachidonic acid.

Entities: Chemical Disease Species

Mesh：

Substances：

Year: 1985 PMID： 3924826 PMCID： PMC262070 DOI： 10.1128/iai.49.1.141-144.1985

Source DB: PubMed Journal: Infect Immun ISSN： 0019-9567 Impact factor: 3.441

12 in total

1. Acute hematogenous osteomyelitis: an experimental model.

Authors: M Deysine; E Rosario; H D Isenberg
Journal: Surgery Date: 1976-01 Impact factor: 3.982

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Authors: C W Norden
Journal: J Infect Dis Date: 1970-11 Impact factor: 5.226

3. Fluid spaces in normal and osteomyelitic canine bone.

Authors: W R Quinlan; B B Hall; R H Fitzgerald
Journal: J Lab Clin Med Date: 1983-07

4. Prostaglandins in orthopaedics.

Authors: A Bennett; W Harvey
Journal: J Bone Joint Surg Br Date: 1981-08

5. Role of prostaglandin-mediated vasodilatation in inflammation.

Authors: T J Williams; M J Peck
Journal: Nature Date: 1977-12-08 Impact factor: 49.962

6. Model of experimental chronic osteomyelitis in rats.

Authors: J P Rissing; T B Buxton; R S Weinstein; R K Shockley
Journal: Infect Immun Date: 1985-03 Impact factor: 3.441

Review 7. Prostaglandins, arachidonic acid, and inflammation.

Authors: F A Kuehl; R W Egan
Journal: Science Date: 1980-11-28 Impact factor: 47.728

8. The hyperalgesic effects of prostacyclin and prostaglandin E2.

Authors: S H Ferreira; M Nakamura; M S de Abreu Castro
Journal: Prostaglandins Date: 1978-07

9. The treatment of osteomyelitis of the tibia with sodium salicylate. An experimental study in rabbits.

Authors: S Dekel; M J Francis
Journal: J Bone Joint Surg Br Date: 1981-08

10. Differential sensitivity of osteoclasts and osteoblasts suggests that prostaglandin E1 effects on bone may be mediated primarily through the osteoclasts.

Authors: G L Wong; B A Kocour
Journal: Arch Biochem Biophys Date: 1983-07-01 Impact factor: 4.013

7 in total

1. Activity of Tedizolid in Methicillin-Resistant Staphylococcus epidermidis Experimental Foreign Body-Associated Osteomyelitis.

Authors: Kyung-Hwa Park; Kerryl E Greenwood-Quaintance; Audrey N Schuetz; Jayawant N Mandrekar; Robin Patel
Journal: Antimicrob Agents Chemother Date: 2017-01-24 Impact factor: 5.191

Arachidonic acid facilitates experimental chronic osteomyelitis in rats.

1. Acute hematogenous osteomyelitis: an experimental model.

2. Experimental osteomyelitis. I. A description of the model.

3. Fluid spaces in normal and osteomyelitic canine bone.

4. Prostaglandins in orthopaedics.

5. Role of prostaglandin-mediated vasodilatation in inflammation.

6. Model of experimental chronic osteomyelitis in rats.

Review 7. Prostaglandins, arachidonic acid, and inflammation.

8. The hyperalgesic effects of prostacyclin and prostaglandin E2.

9. The treatment of osteomyelitis of the tibia with sodium salicylate. An experimental study in rabbits.

10. Differential sensitivity of osteoclasts and osteoblasts suggests that prostaglandin E1 effects on bone may be mediated primarily through the osteoclasts.

1. Activity of Tedizolid in Methicillin-Resistant Staphylococcus epidermidis Experimental Foreign Body-Associated Osteomyelitis.

Review 2. Biomaterials approaches to treating implant-associated osteomyelitis.

Review 3. A Journey into Animal Models of Human Osteomyelitis: A Review.

4. A novel canine model of acute pyogenic spondylodiscitis.

5. Long Bone Osteomyelitis.

Review 6. A systematic review of animal models for Staphylococcus aureus osteomyelitis.

7. In vivo bactericidal efficacy of the Ti6Al4V surface after ultraviolet C treatment.