0000000001033257
AUTHOR
J. Komulainen
The disruption of myofibre structures in skeletal muscle after forced lengthening contractions
Specific antibodies against structural proteins (actin, desmin, dystrophin, fibronectin) of muscle fibres were used to study the effect of forced lengthening contractions on muscle microarchitecture. Tibialis anterior (TA) muscle of male Wistar rats were subjected to 240 forced lengthening contractions. At consecutive time points (0, and 6 h, 2, 4, and 7 days) after stimulation, the TA muscle was excised for biochemical and histological assays. β-Glucuronidase activity, a quantitative indicator of muscle damage, showed increased values 2–7 days after the lengthening, peaking on day 4 (11.7-fold increase). A typical course of histopathological changes (myofibre swelling, necrosis and regener…
CCDC 192292: Experimental Crystal Structure Determination
Related Article: M.S.Hannu-Kuure, J.Komulainen, R.Oilunkaniemi, R.S.Laitinen, R.Suontamo, M.Ahlgren|2003|J.Organomet.Chem.|666|111|doi:10.1016/S0022-328X(02)02108-3
CCDC 192291: Experimental Crystal Structure Determination
Related Article: M.S.Hannu-Kuure, J.Komulainen, R.Oilunkaniemi, R.S.Laitinen, R.Suontamo, M.Ahlgren|2003|J.Organomet.Chem.|666|111|doi:10.1016/S0022-328X(02)02108-3
CCDC 192290: Experimental Crystal Structure Determination
Related Article: M.S.Hannu-Kuure, J.Komulainen, R.Oilunkaniemi, R.S.Laitinen, R.Suontamo, M.Ahlgren|2003|J.Organomet.Chem.|666|111|doi:10.1016/S0022-328X(02)02108-3