I think you're wrong. Not sports related but I did a study on NSAID and lymphedena. And yeah, it does have an effect on inflammation. Yeah, that's my research so I will stand by it.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2791214/?tool=pubmed
Congratulations on doing such fabulous work.
It is only with such investigations that more will be known about the potential effects of NSAIDs.
But such laboratory work is very specific to the animal model and specific type of injury sustained. So in your work:
"Creation of Experimental Lymphedema
Tail lymphedema was induced in female hairless, immunocompetent SKH-1 mice (Charles River Laboratories, Boston, MA) as described [5]. The mice were anesthetized with a solution of ketamine, xylazine, and saline (0.07 ml i.p.). The skin of the tail was circumferentially incised 16 mm distal to its base. The major lymphatic trunks were identified by subcutaneous injection of methylene blue distal to the incision and ablated by limited cautery. The mice were carefully monitored for any visceral signs of distress. Sham surgery controls were treated identically, but without lymphatic cautery. Normal controls did not undergo any surgical manipulation. All mice were sacrificed in accordance with American Veterinary Medical Association guidelines for rodent euthanasia after day 11 days of observation."
"Treatment Protocols
Beginning on day 3 after the surgical manipulation, mice with lymphedema received subcutaneous injections of NSAID (ketoprofen, 5 mg/kg; Sigma, St. Louis, MO) (n=12), sTNF-R1 (pegsunercept, 3 mg/kg; Amgen, Thousand Oaks, CA) (n=17), or phosphate-buffered saline (PBS) (n=16) every other day until the day of sacrifice. Sham surgery and normal controls were treated identically with the NSAID (n=8 per group), sTNF-R1 (n=11 per group), or PBS (n=11 normal controls, n=8 sham surgery controls)."
It is therefore hard to know how this type of injury corresponds to the type of injuries incurred by athletes to muscle, tendon, ligament and cartilage that are associated with overuse syndromes.
It is hard to extend data from observations that were terminated at day 11 as to what the final healing process would have looked like.
It is impossible to know if other NSAIDs taken orally would have the same effect as ketoprofen which was injected subcutaneously.
But I fully hope that this work is precisely a step in the direction you write about as follows:
"We propose that uncoupling the deleterious manifestations of inflammation from the desired pro-lymphangiogenic effects of endogenous repair mechanisms is a logical therapeutic strategy. The present study represents a novel and preliminary step toward the development of pharmacotherapeutics for the treatment of acquired lymphedema."
I fully hope that work such as this will one day revolutionize the entire fields of medicine and surgery by an ability to selectively down regulate deletarious inflammatory responses.
Again, thank you for your work, and thank you for taking the time to draw out attention to it by posting here.