Arthropod diversity in two Historic Gardens in the Azores, Portugal.

The aim of our study was to characterise and compare the richness and composition of endemic, native (non-endemic) and introduced arthropod assemblages of two Azorean Historic Gardens with contrasting plant species composition. We hypothesised that Faial Botanic Garden would hold higher arthropod diversity and abundance of native and endemic arthropod species due to its larger native plant community. Species were collected using several arthropod standardised techniques between April 2017 and June 2018. We used the alpha diversity metrics (Hill series) and the partitioning of total beta diversity (ßtotal) into its replacement (ßrepl) and richness (ßrich) components, to analyse the adult and total arthropod community. The orders Araneae, Coleoptera and Hemiptera were also studied separately. Our results show that the number of exotic arthropod species exceeds the number of native and/or the endemic species in both gardens, but the arthropod community of Faial Botanic Garden exhibited a higher density of endemic and native species. Despite some minor exceptions, the geographic origins of plant communities largely influenced the arthropod species sampled in each garden. This study improves our knowledge about urban arthropod diversity in the Azores and shows how well-designed urban garden management and planning contribute to the conservation of native and endemic Azorean species.

Albuterol isomers modulate platelet-activating factor synthesis and receptor signaling in human bronchial smooth muscle cells.

BACKGROUND: Racemic albuterol is a 50:50 mixture of the (R)- and (S)-enantiomers of albuterol. Its clinical efficacy resides in the (R)-enantiomer (levalbuterol). Studies have shown that (S)-albuterol induces human bronchial smooth muscle cell (HBSMC) proliferation via a pathway linked to platelet-activating factor (PAF), but the underlying mechanism by which (S)-albuterol augments PAF effects is not clear. In this study, we compared effect of levalbuterol and (S)-albuterol on PAF receptor (PAFr)-mediated signaling and PAF metabolism by HBSMCs after incubation with the albuterol isomers. METHODS: PAF binding and inositol phosphate (IP(3)) release were studied on adherent cultured cells. PAFr protein expression was measured by Western blotting, PAF synthesis and catabolism were measured in membrane and cytosolic proteins of cells incubated with albuterol isomers. RESULTS: Compared to control conditions, (S)-albuterol increased PAF binding by 70% after 30 min of preincubation and by 150% after 24 h of preincubation. Levalbuterol had no effect on PAF binding under both conditions. (S)-albuterol also augmented PAF stimulation of IP(3) release, while levalbuterol and the racemic mixture had no effect. WEB 2170, a PAFr antagonist, inhibited the ability of (S)-albuterol to increase PAF binding or stimulate IP(3) release. (S)-albuterol stimulated PAFr protein expression. With PAF metabolism, (S)-albuterol treatment augmented PAF synthesis, but significantly inhibited PAF catabolism. CONCLUSIONS: Our data suggest that one mechanism by which (S)-albuterol stimulates HBSMC proliferation involves upregulation of PAFr-mediated effects including increased PAF synthesis and decreased PAF catabolism.