General clustering of the greatest signalling responses to insulin within the more insulin sensitive individuals (those with higher M values who tended to have lower BMIs) and conversely the lowest signalling responses occur in the more insulin resistant individuals (those with the lower M values who tended to have higher BMIs). However, defects in multiple signalling proteins often co-existed in the same individual but moreover no single signalling defect explained insulin resistance in all obese individuals.DiscussionThe main findings of the current study implicate, for the first time, attenuation of insulin stimulation of the p42/p44 MAP momelotinib cost kinase pathway as an early defect in obesity-induced IR in skeletalmuscle. We observed an impaired insulin-induced stimulation of skeletal muscle p42/p44 MAP kinase activity, in those individuals with higher BMI or lower whole body insulin sensitivity (M value) i.e. obese, IR individuals. Consistent with this finding, in the same individuals, we observed blunting of insulin-induced phosphorylation of p42/p44 MAP kinase at the regulatory residues (Tyr185, Thr183). Importantly, this signalling defect only became apparent when assessing the magnitude of response to insulin, and was not detectable by measuring p42/p44 MAP kinase activity or phosphorylation, in the post-absorptive state, without insulin stimulation. Our findings also suggest that multiple Conduritol B epoxide site molecular mechanisms may mediate skeletal muscle IR within different overweight or obese individuals. Although defective p42/p44 MAP kinase signalling was the most prevalent in the volunteers studied there was clear evidence of defects in other signalling proteins including IRS1 and PKB in several individuals. These observations are entirely consistent with previous analyses from this group demonstrating an association of p42/ p44 MAP kinase signalling with stimulation of muscle glucose transport [17] as well as a defective regulation of the p42/p44 MAP kinase pathway in different pathophysiological conditions associated with skeletal muscle IR and reduced glucose transport. First, in young women with PCOS, there was a severe attenuation of insulin stimulation of the p42/p44 MAP kinase pathway in muscle compared to controls (with p42/p44 MAP kinase activitySkeletal Muscle Signalling Defects in ObesityFigure 4. Relationship of ERK phosphorylation with 25331948 body mass index or M value. Relative ERK phosphorylation according to body mass index (A) or to M value (B) and fold increase in ERK phosphorylation by insulin according to body mass index (r = 0.4; p = 0.07) (C) or to M value (r = 0.59; p = 0.08) (D). doi:10.1371/journal.pone.0056928.gFigure 5. Fold activation of ERK by insulin according to body mass index or M value. (A) Body mass index (r = 0.73; p = 0.0009) or (B) M value (r = 0.52; p = 0.04). doi:10.1371/journal.pone.0056928.gactually reducing in response to insulin) although the group was too small to detect any correlation between BMI and the defective regulation of p42/p44 MAP kinase in the PCOS group [2]. Others have reported that the p42/p44 MAP kinase pathway is constitutively activated both in vitro and in vivo in the skeletal muscle of women with PCOS [18]. Similarly, in older healthy subjects and in patients with T2DM, in whom skeletal muscle uptake of 2-deoxyglucose was blunted compared with healthy young men, reduced stimulation of p42/44 MAP kinase phosphorylation was observed [14]. In contrast, Cusi et al reported that insulin stimulation o.General clustering of the greatest signalling responses to insulin within the more insulin sensitive individuals (those with higher M values who tended to have lower BMIs) and conversely the lowest signalling responses occur in the more insulin resistant individuals (those with the lower M values who tended to have higher BMIs). However, defects in multiple signalling proteins often co-existed in the same individual but moreover no single signalling defect explained insulin resistance in all obese individuals.DiscussionThe main findings of the current study implicate, for the first time, attenuation of insulin stimulation of the p42/p44 MAP kinase pathway as an early defect in obesity-induced IR in skeletalmuscle. We observed an impaired insulin-induced stimulation of skeletal muscle p42/p44 MAP kinase activity, in those individuals with higher BMI or lower whole body insulin sensitivity (M value) i.e. obese, IR individuals. Consistent with this finding, in the same individuals, we observed blunting of insulin-induced phosphorylation of p42/p44 MAP kinase at the regulatory residues (Tyr185, Thr183). Importantly, this signalling defect only became apparent when assessing the magnitude of response to insulin, and was not detectable by measuring p42/p44 MAP kinase activity or phosphorylation, in the post-absorptive state, without insulin stimulation. Our findings also suggest that multiple molecular mechanisms may mediate skeletal muscle IR within different overweight or obese individuals. Although defective p42/p44 MAP kinase signalling was the most prevalent in the volunteers studied there was clear evidence of defects in other signalling proteins including IRS1 and PKB in several individuals. These observations are entirely consistent with previous analyses from this group demonstrating an association of p42/ p44 MAP kinase signalling with stimulation of muscle glucose transport [17] as well as a defective regulation of the p42/p44 MAP kinase pathway in different pathophysiological conditions associated with skeletal muscle IR and reduced glucose transport. First, in young women with PCOS, there was a severe attenuation of insulin stimulation of the p42/p44 MAP kinase pathway in muscle compared to controls (with p42/p44 MAP kinase activitySkeletal Muscle Signalling Defects in ObesityFigure 4. Relationship of ERK phosphorylation with 25331948 body mass index or M value. Relative ERK phosphorylation according to body mass index (A) or to M value (B) and fold increase in ERK phosphorylation by insulin according to body mass index (r = 0.4; p = 0.07) (C) or to M value (r = 0.59; p = 0.08) (D). doi:10.1371/journal.pone.0056928.gFigure 5. Fold activation of ERK by insulin according to body mass index or M value. (A) Body mass index (r = 0.73; p = 0.0009) or (B) M value (r = 0.52; p = 0.04). doi:10.1371/journal.pone.0056928.gactually reducing in response to insulin) although the group was too small to detect any correlation between BMI and the defective regulation of p42/p44 MAP kinase in the PCOS group [2]. Others have reported that the p42/p44 MAP kinase pathway is constitutively activated both in vitro and in vivo in the skeletal muscle of women with PCOS [18]. Similarly, in older healthy subjects and in patients with T2DM, in whom skeletal muscle uptake of 2-deoxyglucose was blunted compared with healthy young men, reduced stimulation of p42/44 MAP kinase phosphorylation was observed [14]. In contrast, Cusi et al reported that insulin stimulation o.
