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dc.contributor.authorPündük, Zekine
dc.contributor.authorOral, Onur
dc.contributor.authorÖzkayın, Nadir
dc.contributor.authorRahman, Khalid
dc.date.accessioned2019-10-23T11:26:32Z
dc.date.available2019-10-23T11:26:32Z
dc.date.issued2014en_US
dc.identifier.issn23259671
dc.identifier.urihttps://hdl.handle.net/20.500.12462/9194
dc.descriptionPündük, Zekine (Balikesir Author)en_US
dc.description.abstractObjectives: Autologous Platelet Rich Plasma (PRP) therapy, is considered to be a promising solution in accelerating the healing process of injured skeletal muscle tissue. In addition to the release of growth factors, PRP also promotes concentrated anti-inflammatory signals, including interleukins. However, the impact of the intramuscular administration of the PRP on hematologic and biochemical responses has not been fully elucidated in exercise induced muscle damage. Methods: Twelve healthy moderately active male volunteers, without previous experience with eccentric/concentric elbow flexors exercise, participated in this study. They were divided into two groups: control group (CONTROL, n=6) and platelet rich plasma administration group (PRP, n=6) group. To induce muscle damage, subjects in both groups performed concentric/eccentric contractions with load of (80% 1RM) maximal voluntary contraction of the elbow flexors until point of exhaustion of the non-dominant arm. The non-dominant arms of the PRP group were treated with autologous PRP (Regen ACR-C, Regen Lab, Switzerland) post-24h exercise induced damage (DOMS). Subsequently, 4 ml PRP samples was injected using a 20-gauge needle into the region of the biceps brachii of the non-dominant arm under sterile aseptic conditions. Venous blood samples were collected pre-, and 4 days post-exercise, and analyzed for complete blood counts, serum ferritin, iron, iron binding capacity (IBC), creatinine kinase (CK), lactate dehydrogenase (LDH), aspartate aminotransferase (AST), alanine aminotransferase (ALT) as markers of muscle damage and inflammation. Results: We found that the baseline levels of iron, ferritin, IBC, CK, LDH, AST and ALT were similar in control and PRP groups. However, 24 h following exercise induced muscle damage a significant increase in these parameters was observed in both groups. Interestingly, PRP administration decreased plasma iron levels compared to the control group but this was only achieved on the second day of post-exercise induced muscle damage. In addition, the plasma IBC levels increased in PRP group from day 2 to 4 post exercise compared to control group. PRP administration had no effect on plasma ferritin, CK, LDH, AST, and LDH levels. Conclusion: Acute exhaustive exercise increased muscle damage markers, including plasma iron, IBC and ferritin levels, indicating metabolic stress due to exercise induced muscle damage. PRP administration decreased the iron levels post-exercise and may have a role to play in the recovery of exercise induced muscle damage.en_US
dc.language.isoengen_US
dc.publisherSAGE Publications Ltden_US
dc.relation.isversionof10.1177/2325967114S00193en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectInjectionsen_US
dc.subjectIronen_US
dc.subjectBQA trainingen_US
dc.titleSingle dose of intra-muscular platlet rich plasma reverses the increase in plasma iron levels in exercise induced muscle damage: A pilot studyen_US
dc.typeotheren_US
dc.relation.journalOrthopaedic Journal of Sports Medicineen_US
dc.contributor.departmentBeden Eğitimi ve Spor Yüksekokuluen_US
dc.identifier.volume2en_US
dc.identifier.issue11en_US
dc.identifier.startpage1en_US
dc.identifier.endpage6en_US
dc.relation.publicationcategoryDiğeren_US


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