The Annals Behind The MCF2L Victory
62 Different exercise modes result in the activation of different fibre types and it should be noted that examination of whole muscle biopsies obtained from the vastus lateralis show a mixture of Type I and Type II fibres. In rodent skeletal muscle, no fibre type dependence on the expression of ��-calpain was seen.13 In contrast, there was approximately 1.9-fold more calpain-3 present in individual muscle fibre segments from EDL (exclusively fast-twitch fibres) compared with those obtained from soleus muscle (predominantly slow-twitch fibres); however, there was considerable overlap of values across the fibre populations from the two muscles.41 Nevertheless, this trend is the opposite to the approximate twofold increase in calpain-3 protein in fast-twitch compared with slow-twitch fibres http://www.selleckchem.com/products/Erlotinib-Hydrochloride.html in porcine skeletal muscle.63 It is not known whether there is a fibre type-dependent distribution of ��-calpain or calpain-3 in human skeletal muscle. Eccentric exercise represents the only physiological circumstance shown to result in the in vivo activation of calpain-3.62 There are two relevant mechanisms that could result in calpain-3 activation during and/or following an eccentric bout of exercise: (i) the muscle fibres are lengthened during muscle contraction; and (ii) the [Ca2+]i would be expected to remain slightly Ponatinib elevated above normal resting cytoplasmic levels for 24�C48?h following the exercise, as seen in rodent muscles.57 Either of these mechanisms may MCF2L feasibly be involved in the activation of calpain-3 following eccentric exercise. First, it has been suggested that calpain-3 becomes activated if its IS2 region is not bound to titin and so its activation may be sensitive to muscle fibre stretching. Second, although it was originally suggested that calpain-3 spontaneously autolysed in a Ca2+-independent manner,39 and recent literature continues to refer to such spontaneous activation of calpain-3,45,64 it has been clearly shown that both recombinantly expressed38,40 and endogenous calpain-3 in rat skeletal muscle17 are very stable at normal resting [Ca2+]; however, calpain-3 autolysis is very sensitive to even small changes in [Ca2+]. To understand potential mechanisms involved in calpain-3 activation following eccentric exercise, the direct effect of these two properties of calpain-3 were examined in individual skeletal muscle fibres. To investigate the effect of stretch per se, solutions containing very low [Ca2+] (