GII showed a higher molecular organization in the d and p regions as detected by measuring optical retardation, a lower concentration of hydroxyproline in the i region and a significant decrease in noncollagenous proteins found in the three regions of the tendon. Regarding the glycosaminoglycans,

diminishing dermatan sulfate and the absence of chondroitin sulfate in the i region were observed in Selleckchem P5091 GII when compared to GI. However, in the same region of GIV, higher concentrations of chondroitin and dermatan sulfate were observed along with a strong metachromasy. An increase in hydroxyproline content in the i region and a higher molecular organization in the d and p regions were observed in GIV. Apparently, the active isoforms of metalloproteinase-2 also increased after stretching in all regions. https://www.selleckchem.com/products/dorsomorphin-2hcl.html These results suggest that stretching after immobilization contributed to the increase in molecular organization and to the synthesis

of extracellular matrix components.”
“Zn2+ is an essential ion that is stored in and co-released from glutamatergic synapses and it modulates neurotransmitter receptors involved in long-term potentiation (LTP). However, the mechanism(s) underlying Zn2+-induced modulation of LTP remain(s) unclear. As the purinergic P2X receptors are relevant targets for Zn2+ action, we have studied ERK screening their role in LTP modulation by Zn2+ in the CA1 region of rat hippocampal slices. Induction of LTP in the presence of Zn2+ revealed a biphasic effect – 5-50 mu m enhanced LTP induction, whereas 100-300 mu m Zn2+ inhibited LTP. The involvement of a purinergic mechanism is supported by the fact that application of the P2X receptor antagonists 2′,3′-O-(2,4,6-trinitrophenyl) ATP (TNP-ATP) and periodate-oxidized ATP fully abolished

the facilitatory effect of Zn2+. Notably, application of the P2X(7) receptor-specific antagonist Brilliant Blue G did not modify the Zn2+-dependent facilitation of LTP. Exogenous ATP also produced a biphasic effect – 0.1-1 mu m ATP facilitated LTP, whereas 5-10 mu m inhibited LTP. The facilitatory effect of ATP was abolished by the application of TNP-ATP and was modified in the presence of 5 mu m Zn2+, suggesting that P2X receptors are involved in LTP induction and that Zn2+ leads to an increase in the affinity of P2X receptors for ATP. The latter confirms our previous results from heterologous expression systems. Collectively, our results indicate that Zn2+ at low concentrations enhances LTP by modulating P2X receptors. Although it is not yet clear which purinergic receptor subtype(s) is responsible for these effects on LTP, the data presented here suggest that P2X(4) but not P2X(7) is involved.