Social Enterprise in Spain: A Diversity of Roots and a Proposal of Models

The term “social enterprise” was first used, at the end of the 1980s, by organisations that promoted the social and labour integration of persons at risk of social and labour exclusion and other similar social activities. The social economy sector has since slowly introduced this term to describe its entities in order to gain recognition by society, and it is working to promote a generally accepted definition of social enterprise’s behaviour based on the principles and values of the social economy (participation, general interest...). According to Article 5 of Spanish Law 5/2011 on the Social Economy, work integration social enterprises and so-called “special employment centres” are part of the social economy, and so are all firms and entities carrying out activities following the values and principles of the social economy sector. In this context, organisations of the social economy sector also are beginning to use the “social enterprise” concept. In Spain, a debate still exists regarding its exact definition. A mix of perspectives on this concept, with different nuances, can be observed. Besides, the current context of reduced governmental budgets and social services in Spain causes social organisations to adopt new approaches to this term of social enterprise, as this type of organisation is more likely to receive funds from the European Union. This paper’s objective is to analyse all perspectives on the concept of social enterprise as well as the various social enterprise models existing in Spain. The document structure is organized as follow. In the first section, we present the context and the main concepts related to social enterprises in this country. In the second section, we provide an analysis of changes in the evolution of social enterprise criteria to identify established models and emerging patterns. In the third section, we put forward another typology, based on institutionalisation stages. Finally, we conclude by recommending an approach to future work and provide a basic bibliography on the subject

Leucine-enriched protein feeding does not impair exercise-induced free fatty acid availability and lipid oxidation: beneficial implications for training in carbohydrate-restricted states

Given that the enhanced oxidative adaptations observed when training in carbohydrate (CHO) restricted states are potentially regulated through free fatty acid (FFA) mediated signalling and that leucine rich protein elevates muscle protein synthesis, the present study aimed to test the hypothesis that leucine enriched protein feeding enhances circulating leucine concentration but does not impair FFA availability nor whole body lipid oxidation 56 during exercise. Nine males cycled for 2 h at 70% VO2peak when fasted (PLACEBO) or having consumed a whey protein solution (WHEY) or a leucine enriched whey protein gel (GEL), administered as 22 g 1 hour pre-exercise, 11 g/h during and 22 g thirty minutes post-exercise. Total leucine administration was 14.4 g and 6.3 in GEL and WHEY, respectively. Mean plasma leucine concentrations were elevated in GEL (P= 0.001) compared 60 with WHEY and PLACEBO (375 ± 100, 272 ± 51, 146 ± 14 μmol.L-1 respectively). No differences (P= 0.153) in plasma FFA (WHEY 0.53 ± 0.30, GEL 0.45 ± 0.25, PLACEBO 0.65 ± 0.30, mmol.L-1) or whole body lipid oxidation during exercise (WHEY 0.37 ± 0.26, GEL 0.36 ± 0.24, PLACEBO 0.34 ± 0.24 g/min) were apparent between trials, despite elevated (P= 0.001) insulin in WHEY and GEL compared with PLACEBO (38 ± 16, 35 ± 16, 22 ± 11 pmol.L-1 respectively). We conclude that leucine enriched protein feeding does not impair FFA availability nor whole body lipid oxidation during exercise, thus having practical applications for athletes who deliberately train in CHO restricted states to promote skeletal muscle adaptations

Postexercise High-Fat Feeding Supresses p70S6K1 Activity in Human Skeletal Muscle.

PURPOSE: To examine the effects of reduced CHO but high post-exercise fat availability on cell signalling and expression of genes with putative roles in regulation of mitochondrial biogenesis, lipid metabolism and muscle protein synthesis (MPS). METHODS: Ten males completed a twice per day exercise model (3.5 h between sessions) comprising morning high-intensity interval (HIT) (8 x 5-min at 85% VO2peak) and afternoon steady-state (SS) running (60 min at 70% VO2peak). In a repeated measures design, runners exercised under different isoenergetic dietary conditions consisting of high CHO (HCHO: 10 CHO, 2.5 Protein and 0.8 Fat g.kg per whole trial period) or reduced CHO but high fat availability in the post-exercise recovery periods (HFAT: 2.5 CHO, 2.5 Protein and 3.5 Fat g.kg per whole trial period). RESULTS: Muscle glycogen was lower (P<0.05) at 3 (251 vs 301 mmol.kgdw) and 15 h (182 vs 312 mmol.kgdw) post-SS exercise in HFAT compared to HCHO. AMPK-α2 activity was not increased post-SS in either condition (P=0.41) though comparable increases (all P<0.05) in PGC-1α, p53, CS, Tfam, PPAR and ERRα mRNA were observed in HCHO and HFAT. In contrast, PDK4 (P=0.003), CD36 (P=0.05) and CPT1 (P=0.03) mRNA were greater in HFAT in the recovery period from SS exercise compared with HCHO. p70S6K activity was higher (P=0.08) at 3 h post-SS exercise in HCHO versus HFAT (72.7 ± 51.9 vs 44.7 ± 27 fmol.min mg). CONCLUSION: Post-exercise high fat feeding does not augment mRNA expression of genes associated with regulatory roles in mitochondrial biogenesis though it does increase lipid gene expression. However, post-exercise p70S6K1 activity is reduced under conditions of high fat feeding thus potentially impairing skeletal muscle remodelling processes

Differences in salivary hormones and perception of exertion in elite women and men volleyball players during tournament.

BACKGROUND: Sports tournaments induce both psychological and physiological stress, which seems to be different between men and women. Competition induces anticipatory rises in testosterone and cortisol levels, which may affect performance and physical exertion during tournaments. The aim of this study was to compare the changes in salivary cortisol and testosterone concentrations between men and women during an official volleyball tournament and to test potential correlations between changes in these hormones and perceived exertion after match. METHODS: Three matches of each team were assessed in the group stage of the Men and Women South American Volleyball Championship. Salivary cortisol and testosterone levels were measured in the fasting state, before and after each match. The rate of perceived exertion (RPE) was assessed after each match. RESULTS: Fasting cortisol concentrations were higher in women than men (~25%, P<0.001) while fasting testosterone was higher in men than women (~46%, P<0.001). Cortisol concentration increased only after the second match in men (+53.7%, P<0.001). Testosterone concentration was low before and after the third match in men (P<0.001) while it was elevated after the third match in women (P=0.003). The rate of perceived exertion was correlated with the change in testosterone levels due to the matches in both women (r=0.33; P=0.04) and men (r=0.44; P=0.02), which was not observed for cortisol concentrations. CONCLUSIONS: These results indicate that women have higher fasting cortisol, but lower fasting testosterone concentrations than men during a volleyball tournament. Thus, hormonal responses of women and men are different and related to their effort during the matches

A mutation in desmin makes skeletal muscle less vulnerable to acute muscle damage after eccentric loading in rats.

Desminopathy is the most common intermediate filament disease in humans. The most frequent mutation causing desminopathy in patients is a R350P DES missense mutation. We have developed a rat model with an analogous mutation in R349P Des. To investigate the role of R349P Des in mechanical loading, we stimulated the sciatic nerve of wild-type littermates (WT) (n&nbsp;=&nbsp;6) and animals carrying the mutation (MUT) (n&nbsp;=&nbsp;6) causing a lengthening contraction of the dorsi flexor muscles. MUT animals showed signs of ongoing regeneration at baseline as indicated by a higher number of central nuclei (genotype: P&nbsp;&lt;&nbsp;.0001). While stimulation did not impact central nuclei, we found an increased number of IgG positive fibers (membrane damage indicator) after eccentric contractions with both genotypes (stimulation: P&nbsp;&lt;&nbsp;.01). Interestingly, WT animals displayed a more pronounced increase in IgG positive fibers with stimulation compared to MUT (interaction: P&nbsp;&lt;&nbsp;.05). In addition to altered histology, molecular signaling on the protein level differed between WT and MUT. The membrane repair protein dysferlin decreased with eccentric loading in WT but increased in MUT (interaction: P&nbsp;&lt;&nbsp;.05). The autophagic substrate p62 was increased in both genotypes with loading (stimulation: P&nbsp;&lt;&nbsp;.05) but tended to be more elevated in WT (interaction: P&nbsp;=&nbsp;.05). Caspase 3 levels, a central regulator of apoptotic cell death, was increased with stimulation in both genotypes (stimulation: P&nbsp;&lt;&nbsp;.01) but more so in WT animals (interaction: P&nbsp;&lt;&nbsp;.0001). Overall, our data indicate that R349P Des rats have a lower susceptibility to structural muscle damage of the cytoskeleton and sarcolemma with acute eccentric loading

Programmed death ligand-1 expression on donor T cells drives graft-versus-host disease lethality.

Programmed death ligand-1 (PD-L1) interaction with PD-1 induces T cell exhaustion and is a therapeutic target to enhance immune responses against cancer and chronic infections. In murine bone marrow transplant models, PD-L1 expression on host target tissues reduces the incidence of graft-versus-host disease (GVHD). PD-L1 is also expressed on T cells; however, it is unclear whether PD-L1 on this population influences immune function. Here, we examined the effects of PD-L1 modulation of T cell function in GVHD. In patients with severe GVHD, PD-L1 expression was increased on donor T cells. Compared with mice that received WT T cells, GVHD was reduced in animals that received T cells from Pdl1-/- donors. PD-L1–deficient T cells had reduced expression of gut homing receptors, diminished production of inflammatory cytokines, and enhanced rates of apoptosis. Moreover, multiple bioenergetic pathways, including aerobic glycolysis, oxidative phosphorylation, and fatty acid metabolism, were also reduced in T cells lacking PD-L1. Finally, the reduction of acute GVHD lethality in mice that received Pdl1-/- donor cells did not affect graft-versus-leukemia responses. These data demonstrate that PD-L1 selectively enhances T cell–mediated immune responses, suggesting a context-dependent function of the PD-1/PD-L1 axis, and suggest selective inhibition of PD-L1 on donor T cells as a potential strategy to prevent or ameliorate GVHD