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Madani, G.

Publications and source records attributed to Madani, G..

2 recordsLinked to original sources

Its just a phase: moonlight and rainfall influence the activity of a threatened cave-roosting bat in the Pilbara

Wildlife monitoring in arid environments is complicated by substantial temporal and spatial variation in animal activity driven by unpredictable environmental conditions. For highly mobile species, movements across the landscape may further influence activity recorded at fixed monitoring locations, raising questions about whether short-term surveys adequately represent patterns of site use. We examined temporal variation in acoustic activity of the threatened Pilbara Leaf-nosed Bat (Rhinonicteris aurantia Pilbara form), a highly mobile, cave-roosting insectivorous bat inhabiting the arid Pilbara region of north-western Australia. Acoustic activity was monitored continuously at two permanent diurnal roosts for up to two years, comprising 1601 detector-nights across three detector locations. We tested relationships between nightly activity and environmental conditions, detector location and anthropogenic disturbance. Activity varied substantially through time and among detector locations. Moon illumination and cumulative rainfall were strongly associated with activity, but their interaction differed between roosts: activity was highest under low moon illumination and low cumulative rainfall at Chateau Cave, whereas activity at Daltons was highest under low moon illumination and higher cumulative rainfall. Activity also differed markedly between detector positions within Chateau Cave, and humidity, temperature and artificial light at night had additional location-specific effects. Other measures of anthropogenic disturbance, including cave entry, blasting and mining activity, had comparatively weak support. The contrasting environmental relationships among locations demonstrate that acoustic activity at permanent roosts is strongly context dependent. For a species capable of extensive movements among roosts, temporal variation in activity may reflect behavioural responses and redistribution of individuals across the landscape rather than rapid demographic change. We suggest that facultative nomadism may provide a useful hypothesis for understanding temporal variation in roost use by Pilbara Leaf-nosed Bat. More broadly, our results demonstrate that short-duration acoustic surveys of highly mobile species in arid environments may provide an incomplete representation of longer-term site use and should incorporate temporal replication and environmental context when used for conservation and impact assessment.

ecology↗

Antidepressants are complex regulators of lipoprotein(a) macropinocytosis

We recently found that plasminogen receptors regulate the plasma membrane binding and uptake of Lp(a) via macropinocytosis. In this study, we sought to further define lipoprotein(a) [Lp(a)] macropinocytosis, discovering an unexpected role for antidepressants and serotonin in the regulation of this process. We found that the tricyclic antidepressant imipramine enhanced Lp(a) uptake, in contradiction of its published role as a macropinocytosis inhibitor. Extending these experiments to the commonly used serotonin uptake inhibitors (SSRIs) citalopram and sertraline, we found that citalopram stimulated, while sertraline inhibited, Lp(a) uptake. Imipramine and citalopram enhanced cell surface binding of Lp(a) rather than upregulating macropinocytosis. Consistent with imipramine and citalopram boosting extracellular serotonin levels, serotonin itself also enhanced Lp(a) surface binding and uptake. Imipramine and serotonin increased expression of the plasminogen receptor with a C-terminal lysine (PlgRKT), a receptor known to enhance cell surface binding of Lp(a), likely accounting for their effects on Lp(a) uptake. Finally, imipramine and citalopram increased Lp(a) delivery into Rab11 recycling endosomes, but not degradative pathways in the cell. These findings indicate citalopram and imipramine may have utility as a potential Lp(a)-lowering therapeutic in people suffering from depression who often have elevated Lp(a) levels and an increased risk of cardiovascular disease.

cell biology↗