Measurement of cytosolic free Ca2+ in individual pancreatic acini

The kinetics of changes in cytosolic free Ca2+ ([Ca2+]i) were determined in individual rat pancreatic acini by microfluorimetry. Three major findings are reported. First, at maximal stimulatory concentrations for amylase release, both caerulein and bombesin induced an initial rise in [Ca2+]i followed by prolonged secondary oscillations of smaller amplitude. The latter effect was not observed with supramaximal doses of caerulein. Second, these cyclic changes were dependent, at least in part, on extracellular Ca2+. Finally, comparison of the threshold doses for [Ca2+]i mobilization and enzyme discharge demonstrated that pathways independent of an elevation of [Ca2+]i control the secretory activity of pancreatic acini at low, picomolar agonist concentrations.     

Coordinated regulation of free Ca2+ by isolated organelles from a rat insulinoma

Experiments aimed at the partial reconstitution of the intracellular transport systems regulating the cytosolic free Ca2+ homeostasis are reported. Rat insulinoma subcellular fractions enriched in mitochondria, endoplasmic reticulum (microsomes), and secretory granules were studied. The ambient free Ca2+ concentration maintained by the separate or combined organelles was determined with a Ca2+-selective minielectrode. The data demonstrate that ambient [Ca2+] is established by the microsomes, not by the mitochondria or the secretory granules, in the range of resting cytosolic Ca2+ concentrations (0.1-0.2 microM Ca2+). Furthermore, the microsomes are able to deplete largely the mitochondria of their exchangeable calcium. Nonetheless, both mitochondria and microsomes, but not secretory granules, function as a coordinated unit to restore the previous ambient [Ca2+] following its perturbation. Thus, mitochondria play a major role in bringing down rapidly ambient [Ca2+] to the submicromolar range, whereas the endoplasmic reticulum acts as a relay in the transport mechanisms which lower [Ca2+] to the resting level.     

Similar hypotensive responses to resistance exercise with and without blood flow restriction

Low intensity resistance exercise (RE) with blood flow restriction (BFR) has gained attention in the literature due to the beneficial effects on functional and morphological variables, similar to those observed during traditional RE without BFR, while the effects of BFR on post-exercise hypotension remain unclear. The aim of the present study was to compare the blood pressure (BP) response of trained normotensive individuals to RE with and without BFR. In this cross-over randomized trial, eight male subjects (23.8 ± 4 years, 74 ± 3 kg, 174 ± 4 cm) completed two exercise protocols: traditional RE (3 x 10 repetitions at 70% one-repetition maximum [1-RM]) and low intensity RE (3 x 15 repetitions at 20% 1-RM) with BFR. Blood pressure measurements were performed after 15 min of seated rest (0), immediately after and 10 min, 20 min, 30 min, 40 min, 50 min and 60 min after the experimental sessions. Similar hypotensive effects for systolic BP (SBP) were observed for both protocols (P < 0.05) after exercise, with no differences between groups (P > 0.05) and no statistically significant difference for diastolic BP (P > 0.05). These results suggest that in normotensive trained individuals, both traditional RE and RE with BFR induce hypotension for SBP, which is important to prevent cardiovascular disturbances.     

Climate variability masks the impacts of land use change on nutrient export in a suburbanizing watershed

Suburbanization negatively impacts aquatic systems by altering hydrology and nutrient loading. These changes interact with climate and aquatic ecosystem processes to alter nutrient flux dynamics. We used a long term data set (1993–2009) to investigate the influence of suburbanization, climate, and in-stream processes on nitrogen and phosphorus export in rivers draining the Ipswich and Parker River watersheds in northeastern MA, USA. During this timeframe population density increased in these watersheds by 14 % while precipitation varied by 46 %. We compared nutrient export patterns from the two larger watersheds with those from two nested headwater catchments collected over a nine year period (2001–2009). The headwater catchments were of contrasting, but stable, land uses that dominate the larger watersheds (suburban and forested). Despite ongoing land use change and an increase in population density in the mainstem watersheds, we did not detect an increase in dissolved inorganic nitrogen (DIN) or PO₄ concentration or export over the 16-year time period. Inter-annual climate and associated runoff variability was the major control. Annual DIN and PO₄ export increased with greater annual precipitation in the Ipswich and the Parker River watersheds, as well as the forested headwater catchment. In contrast, annual DIN export fluxes from the suburban headwater catchment were less affected by precipitation variability, with inter-annual export fluxes negatively correlated with mean annual temperature. The larger watershed exports diverged from headwater exports, particularly during summer, low-flow periods, suggesting retention of DIN and PO₄. Our study shows suburban headwater exports respond to inter-annual variation in runoff and climate differently than forested headwater exports, but the impacts from headwater streams could be buffered by the river network. The net effect is that inter-annual variation and network buffering can mitigate higher nutrient exports from larger suburbanizing watersheds over decadal time periods.     

Mitochondrial matrix calcium is an activating signal for hormone secretion

Mitochondrial Ca(2+) signals have been proposed to accelerate oxidative metabolism and ATP production to match Ca(2+)-activated energy-consuming processes. Efforts to understand the signaling role of mitochondrial Ca(2+) have been hampered by the inability to manipulate matrix Ca(2+) without directly altering cytosolic Ca(2+). We were able to selectively buffer mitochondrial Ca(2+) rises by targeting the Ca(2+)-binding protein S100G to the matrix. We find that matrix Ca(2+) controls signal-dependent NAD(P)H formation, respiration, and ATP changes in intact cells. Furthermore, we demonstrate that matrix Ca(2+) increases are necessary for the amplification of sustained glucose-dependent insulin secretion in β cells. Through the regulation of NAD(P)H in adrenal glomerulosa cells, matrix Ca(2+) also acts as a positive signal in reductive biosynthesis, which stimulates aldosterone secretion. Our dissection of cytosolic and mitochondrial Ca(2+) signals reveals the physiological importance of matrix Ca(2+) in energy metabolism required for signal-dependent hormone secretion.