After 2 5 mg/kg MDMA, mean MDMA C-max was 164 +/- 47 1 ng/ml, HHM

After 2.5 mg/kg MDMA, mean MDMA C-max was 164 +/- 47.1 ng/ml, HHMA and HMMA were major metabolites, and smaller than 20% of MDMA was metabolized to MDA. After 5- and 10-mg/ kg doses, MDMA areas under the curve (AUCs) were 3- and 10-fold

greater GDC-0973 in vivo than those after 2.5 mg/kg; HHMA and HMMA AUC values were relatively constant across doses; and MDA AUC values were greater than dose-proportional. Our data provide decisive in vivo evidence that MDMA and MDA display nonlinear accumulation via metabolic autoinhibition in the rat. Importantly, 5-HT syndrome severity correlated with MDMA concentrations (r = 0.8083; P smaller than 0.0001) and core temperature correlated with MDA concentrations (r = 0.7595; P smaller than 0.0001), suggesting that MDMA’s behavioral and hyperthermic effects may involve distinct mechanisms. Given key similarities between MDMA pharmacokinetics in rats and humans, data from rats can

be useful when provided at clinically relevant doses.”
“Marine vegetated habitats, e.g. seagrass Vorinostat Epigenetics inhibitor meadows, deliver essential functions and services to coastal ecosystems and human welfare. Impacts induced by humans, however, have facilitated the replacement of seagrasses by alternative vegetation, e.g. green rhizophytic seaweeds. The implications of habitat shifts for ecosystem attributes and processes and the services they deliver remain poorly known. In this study, we compared ecosystem structure and function between Cymodocea nodosa seagrass meadows and bottoms dominated by Caulerpa prolifera, a green, native, rhizophytic seaweed, through 5 ecological proxies: (i) primary production buy CA4P (via

community metabolism), (ii) composition and abundance of epifauna (a proxy for provision of habitat for epifauna), composition and abundance of (iii) small-sized (juvenile) and (iv) large-sized (adult) fishes (proxies for provision of habitat for fishes), and (v) sediment retention (a proxy for sediment stabilization). Four of these proxies were greater in C nodosa seagrass meadows than in C. prolifera beds: gross primary productivity (similar to 1.4 times), the total abundance, species density and biomass of small-sized fishes (similar to 2.1, 13 and 1.3 times, respectively), the total abundance and species density of large-sized fishes (similar to 3.6 and 1.5 times, respectively), and sediment stabilization (similar to 1.4 times). In contrast, the total abundance and species density of epifauna was larger (similar to 3.1 and 1.7 times, respectively) in C prolifera than in C. nodosa seagrass beds. These results suggest that ecosystem structure and function may differ if seagrasses are replaced by green rhizophytic seaweeds. Importantly, ecosystem functions may not be appropriate surrogates for one another.

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