Calcium Transient and Quantal Release in Mouse Neuromuscular Junction Under Extracellular Calcium Concentration Change

2018 ◽  
Vol 8 (4) ◽  
pp. 984-987
Author(s):  
Dmitry V. Samigullin ◽  
Nikita V. Zhilyakov ◽  
Eduard F. Khaziev ◽  
Ellya A. Bukharaeva ◽  
Eugeny E. Nikolsky
2017 ◽  
Vol 313 (3) ◽  
pp. R202-R210 ◽  
Author(s):  
Dengyun Ge ◽  
Nickolas Lavidis

Amphibian neuromuscular junctions (NMJs) are composed of hundreds of neurotransmitter release sites that exhibit nonuniform transmitter release probabilities and demonstrated seasonal modulation. We examined whether recruitment of release sites is variable when the extracellular calcium concentration ([Ca2+]o) is increased in the wet and dry seasons. The amount of transmitter released from the entire nerve terminal increases by approximately the fourth power as [Ca2+]o is increased. Toad ( Bufo marinus) NMJs were visualized using 3,3′-diethyloxardicarbocyanine iodide [DiOC2(5)] fluorescence, and focal loose patch extracellular recordings were used to record the end-plate currents (EPCs) from small groups of release sites. Quantal content ( m̄e), average probability of quantal release ( pe), and the number of active release sites ( ne) were determined for different [Ca2+]o. Our results indicated that the recruitment of quantal release sites with increasing [Ca2+]o differs spatially (between different groups of release sites) and also temporally (in different seasons). These differences were reflected by the nonuniform alterations in pe and ne. Most release site groups demonstrated an increase in both pe and ne when [Ca2+]o increased. In ~30% of release site groups examined, pe decreased while ne increased only during the active period (wet season). Although the dry season induced parallel right shift in the quantal release versus extracellular calcium concentration when compared with the wet season, the dependence of quantal content on [Ca2+]o was not changed. These results demonstrate the flexibility, reserve, and adaptive capacity of neuromuscular junctions in maintaining appropriate levels of neurotransmission.


Endocrine ◽  
2021 ◽  
Vol 71 (3) ◽  
pp. 611-617
Author(s):  
Judit Tőke ◽  
Gábor Czirják ◽  
Péter Enyedi ◽  
Miklós Tóth

AbstractThe calcium-sensing receptor (CaSR) provides the major mechanism for the detection of extracellular calcium concentration in several cell types, via the induction of G-protein-coupled signalling. Accordingly, CaSR plays a pivotal role in calcium homeostasis, and the CaSR gene defects are related to diseases characterized by serum calcium level changes. Activating mutations of the CaSR gene cause enhanced sensitivity to extracellular calcium concentration resulting in autosomal dominant hypocalcemia or Bartter-syndrome type V. Inactivating CaSR gene mutations lead to resistance to extracellular calcium. In these cases, familial hypocalciuric hypercalcaemia (FHH1) or neonatal severe hyperparathyroidism (NSHPT) can develop. FHH2 and FHH3 are associated with mutations of genes of partner proteins of calcium signal transduction. The common polymorphisms of the CaSR gene have been reported not to affect the calcium homeostasis itself; however, they may be associated with the increased risk of malignancies.


1978 ◽  
Vol 33 (7-8) ◽  
pp. 574-579 ◽  
Author(s):  
H. Stieve ◽  
M. Bruns

Abstract The membrane potential in the dark and the saturated response height of the ventral nerve photoreceptor of Limulus was measured by an intracellular electrode while the external concentration of calcium, magnesium and sodium ions was varied. Decreasing the extracellular calcium concentration from 10-2 mol/l causes a calcium-dependent lowering of the dark membrane potential and at very low concentrations (<10-8 mol/l a reversal to ca. +5 to +11 mV, if the external magnesium concentration is also low. Also, the light response diminishes with decreasing extracellular calcium concentration and disappears at a concentration of 10-9 mol/l. External magnesium can substitute for certain properties of extracellular calcium. Lowering the extracellular sodium concentration from 543 mmol/l to 30 - 50 mmol/1 reduces the dark membrane potential and the light responses at normal calcium concentration, whereas at low calcium concentration it causes a substantial rise of both. Interpretation: The results are in accordance with our working hypothesis that a strong reduction of the external calcium (and magnesium) concentration causes a calcium concentration dependent opening of “ light channels” in the dark. Additional lowering the extracellular sodium concentration counteracts this effect; opening and closing of light channels is controlled by negative binding sites on the cell membrane for which calcium and sodium ions compete with an antagonistic action.


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