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. 1994 Dec 1;481(Pt 2):251–271. doi: 10.1113/jphysiol.1994.sp020436

Regulation of intracellular calcium and calcium buffering properties of rat isolated neurohypophysial nerve endings.

E L Stuenkel 1
PMCID: PMC1155926  PMID: 7738824

Abstract

1. Electrophysiological measurements of Ca2+ influx using patch clamp methodology were combined with fluorescent monitoring of the free intracellular calcium concentration ([Ca2+]i) to determine mechanisms of Ca2+ regulation in isolated nerve endings from the rat neurohypophysis. 2. Application of step depolarizations under voltage clamp resulted in voltage-dependent calcium influx (ICa) and increase in the [Ca2+]i. The increase in [Ca2+]i was proportional to the time-integrated ICa for low calcium loads but approached an asymptote of [Ca2+]i at large Ca2+ loads. These data indicate the presence of two distinct rapid Ca2+ buffering mechanisms. 3. Dialysis of fura-2, which competes for Ca2+ binding with the endogenous Ca2+ buffers, reduced the amplitude and increased the duration of the step depolarization-evoked Ca2+ transients. More than 99% of Ca2+ influx at low Ca2+ loads is immediately buffered by this endogenous buffer component, which probably consists of intracellular Ca2+ binding proteins. 4. The capacity of the endogenous buffer for binding Ca2+ remained stable during 300 s of dialysis of the nerve endings. These properties indicated that this Ca2+ buffer component was either immobile or of high molecular weight and slowly diffusible. 5. In the presence of large Ca2+ loads a second distinct Ca2+ buffer mechanism was resolved which limited increases in [Ca2+]i to approximately 600 nM. This Ca2+ buffer exhibited high capacity but low affinity for Ca2+ and its presence resulted in a loss of proportionality between the integrated ICa and the increase in [Ca2+]i. This buffering mechanism was sensitive to the mitochondrial Ca2+ uptake inhibitor Ruthenium Red. 6. Basal [Ca2+]i, depolarization-induced changes in [Ca2+]i and recovery of [Ca2+]i to resting levels following an induced increase in [Ca2+]i were unaffected by thapsigargin and cyclopiazonic acid, specific inhibitors of intracellular Ca(2+)-ATPases. Caffeine and ryanodine were also without effect on Ca2+ regulation. 7. Evoked increases in [Ca2+]i, as well as rates of recovery from a Ca2+ load, were unaffected by the extracellular [Na+], suggesting a minimal role for Na(+)-Ca2+ exchange in Ca2+ regulation in these nerve endings. 8. Application of repetitive step depolarizations for a constant period of stimulation resulted in a proportional frequency (up to 40 Hz)-dependent increase in [Ca2+]i. On the other hand, for a constant number of stimuli a reduction in the [Ca2+]i. On the other hand, for a constant number of stimuli a reduction in the [Ca2+]i increase per impulse was observed at higher frequencies.(ABSTRACT TRUNCATED AT 250 WORDS)

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Selected References

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  1. Ahmed Z., Connor J. A. Calcium regulation by and buffer capacity of molluscan neurons during calcium transients. Cell Calcium. 1988 Apr;9(2):57–69. doi: 10.1016/0143-4160(88)90025-5. [DOI] [PubMed] [Google Scholar]
  2. Artalejo C. R., Adams M. E., Fox A. P. Three types of Ca2+ channel trigger secretion with different efficacies in chromaffin cells. Nature. 1994 Jan 6;367(6458):72–76. doi: 10.1038/367072a0. [DOI] [PubMed] [Google Scholar]
  3. Augustine G. J., Charlton M. P., Smith S. J. Calcium action in synaptic transmitter release. Annu Rev Neurosci. 1987;10:633–693. doi: 10.1146/annurev.ne.10.030187.003221. [DOI] [PubMed] [Google Scholar]
  4. Augustine G. J., Neher E. Calcium requirements for secretion in bovine chromaffin cells. J Physiol. 1992 May;450:247–271. doi: 10.1113/jphysiol.1992.sp019126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Baker P. F., McNaughton P. A. Kinetics and energetics of calcium efflux from intact squid giant axons. J Physiol. 1976 Jul;259(1):103–144. doi: 10.1113/jphysiol.1976.sp011457. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Blaustein M. P., Ector A. C. Carrier-mediated sodium-dependent and calcium-dependent calcium efflux from pinched-off presynaptic nerve terminals (synaptosomes) in vitro. Biochim Biophys Acta. 1976 Jan 21;419(2):295–308. doi: 10.1016/0005-2736(76)90355-2. [DOI] [PubMed] [Google Scholar]
  7. Blaustein M. P., Ratzlaff R. W., Kendrick N. C., Schweitzer E. S. Calcium buffering in presynaptic nerve terminals. I. Evidence for involvement of a nonmitochondrial ATP-dependent sequestration mechanism. J Gen Physiol. 1978 Jul;72(1):15–41. doi: 10.1085/jgp.72.1.15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Blaustein M. P., Ratzlaff R. W., Schweitzer E. S. Calcium buffering in presynaptic nerve terminals. II. Kinetic properties of the nonmitochondrial Ca sequestration mechanism. J Gen Physiol. 1978 Jul;72(1):43–66. doi: 10.1085/jgp.72.1.43. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Bourque C. W. Intraterminal recordings from the rat neurohypophysis in vitro. J Physiol. 1990 Feb;421:247–262. doi: 10.1113/jphysiol.1990.sp017943. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Brethes D., Dayanithi G., Letellier L., Nordmann J. J. Depolarization-induced Ca2+ increase in isolated neurosecretory nerve terminals measured with fura-2. Proc Natl Acad Sci U S A. 1987 Mar;84(5):1439–1443. doi: 10.1073/pnas.84.5.1439. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Brinley F. J., Jr, Tiffert T., Scarpa A., Mullins L. J. Intracellular calcium buffering capacity in isolated squid axons. J Gen Physiol. 1977 Sep;70(3):355–384. doi: 10.1085/jgp.70.3.355. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Cazalis M., Dayanithi G., Nordmann J. J. Hormone release from isolated nerve endings of the rat neurohypophysis. J Physiol. 1987 Sep;390:55–70. doi: 10.1113/jphysiol.1987.sp016686. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Cazalis M., Dayanithi G., Nordmann J. J. The role of patterned burst and interburst interval on the excitation-coupling mechanism in the isolated rat neural lobe. J Physiol. 1985 Dec;369:45–60. doi: 10.1113/jphysiol.1985.sp015887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Dayanithi G., Martin-Moutot N., Barlier S., Colin D. A., Kretz-Zaepfel M., Couraud F., Nordmann J. J. The calcium channel antagonist omega-conotoxin inhibits secretion from peptidergic nerve terminals. Biochem Biophys Res Commun. 1988 Oct 14;156(1):255–262. doi: 10.1016/s0006-291x(88)80833-7. [DOI] [PubMed] [Google Scholar]
  15. Friel D. D., Tsien R. W. A caffeine- and ryanodine-sensitive Ca2+ store in bullfrog sympathetic neurones modulates effects of Ca2+ entry on [Ca2+]i. J Physiol. 1992 May;450:217–246. doi: 10.1113/jphysiol.1992.sp019125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Grynkiewicz G., Poenie M., Tsien R. Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem. 1985 Mar 25;260(6):3440–3450. [PubMed] [Google Scholar]
  17. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  18. Jackson M. B., Konnerth A., Augustine G. J. Action potential broadening and frequency-dependent facilitation of calcium signals in pituitary nerve terminals. Proc Natl Acad Sci U S A. 1991 Jan 15;88(2):380–384. doi: 10.1073/pnas.88.2.380. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Katz B., Miledi R. The timing of calcium action during neuromuscular transmission. J Physiol. 1967 Apr;189(3):535–544. doi: 10.1113/jphysiol.1967.sp008183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Kuba K., Nishi S. Rhythmic hyperpolarizations and depolarization of sympathetic ganglion cells induced by caffeine. J Neurophysiol. 1976 May;39(3):547–563. doi: 10.1152/jn.1976.39.3.547. [DOI] [PubMed] [Google Scholar]
  21. Lemos J. R., Nowycky M. C. Two types of calcium channels coexist in peptide-releasing vertebrate nerve terminals. Neuron. 1989 May;2(5):1419–1426. doi: 10.1016/0896-6273(89)90187-6. [DOI] [PubMed] [Google Scholar]
  22. Lim N. F., Nowycky M. C., Bookman R. J. Direct measurement of exocytosis and calcium currents in single vertebrate nerve terminals. Nature. 1990 Mar 29;344(6265):449–451. doi: 10.1038/344449a0. [DOI] [PubMed] [Google Scholar]
  23. Lindau M., Stuenkel E. L., Nordmann J. J. Depolarization, intracellular calcium and exocytosis in single vertebrate nerve endings. Biophys J. 1992 Jan;61(1):19–30. doi: 10.1016/S0006-3495(92)81812-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Lindgren C. A., Moore J. W. Calcium current in motor nerve endings of the lizard. Ann N Y Acad Sci. 1991;635:58–69. doi: 10.1111/j.1749-6632.1991.tb36481.x. [DOI] [PubMed] [Google Scholar]
  25. Llinás R., Steinberg I. Z., Walton K. Presynaptic calcium currents and their relation to synaptic transmission: voltage clamp study in squid giant synapse and theoretical model for the calcium gate. Proc Natl Acad Sci U S A. 1976 Aug;73(8):2918–2922. doi: 10.1073/pnas.73.8.2918. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Moore C. L. Specific inhibition of mitochondrial Ca++ transport by ruthenium red. Biochem Biophys Res Commun. 1971 Jan 22;42(2):298–305. doi: 10.1016/0006-291x(71)90102-1. [DOI] [PubMed] [Google Scholar]
  27. Nachshen D. A. Regulation of cytosolic calcium concentration in presynaptic nerve endings isolated from rat brain. J Physiol. 1985 Jun;363:87–101. doi: 10.1113/jphysiol.1985.sp015697. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Neher E., Augustine G. J. Calcium gradients and buffers in bovine chromaffin cells. J Physiol. 1992 May;450:273–301. doi: 10.1113/jphysiol.1992.sp019127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Nicaise G., Maggio K., Thirion S., Horoyan M., Keicher E. The calcium loading of secretory granules. A possible key event in stimulus-secretion coupling. Biol Cell. 1992;75(2):89–99. doi: 10.1016/0248-4900(92)90128-n. [DOI] [PubMed] [Google Scholar]
  30. Nicholls D. G. Regulation of calcium in isolated nerve terminals (synaptosomes): relationship to neurotransmitter release. Ann N Y Acad Sci. 1989;568:81–88. doi: 10.1111/j.1749-6632.1989.tb12493.x. [DOI] [PubMed] [Google Scholar]
  31. Nordmann J. J., Dayanithi G., Lemos J. R. Isolated neurosecretory nerve endings as a tool for studying the mechanism of stimulus-secretion coupling. Biosci Rep. 1987 May;7(5):411–426. doi: 10.1007/BF01362504. [DOI] [PubMed] [Google Scholar]
  32. Nordmann J. J., Stuenkel E. L. Electrical properties of axons and neurohypophysial nerve terminals and their relationship to secretion in the rat. J Physiol. 1986 Nov;380:521–539. doi: 10.1113/jphysiol.1986.sp016300. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Nordmann J. J. Ultrastructural morphometry of the rat neurohypophysis. J Anat. 1977 Feb;123(Pt 1):213–218. [PMC free article] [PubMed] [Google Scholar]
  34. Nordmann J. J., Zyzek E. Calcium efflux from the rat neurohypophysis. J Physiol. 1982 Apr;325:281–299. doi: 10.1113/jphysiol.1982.sp014150. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Obaid A. L., Flores R., Salzberg B. M. Calcium channels that are required for secretion from intact nerve terminals of vertebrates are sensitive to omega-conotoxin and relatively insensitive to dihydropyridines. Optical studies with and without voltage-sensitive dyes. J Gen Physiol. 1989 Apr;93(4):715–729. doi: 10.1085/jgp.93.4.715. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Onodera K. Effect of caffeine on the neuromuscular junction of the frog, and its relation to external calcium concentration. Jpn J Physiol. 1973 Dec;23(6):587–597. doi: 10.2170/jjphysiol.23.587. [DOI] [PubMed] [Google Scholar]
  37. Poulain D. A., Wakerley J. B. Electrophysiology of hypothalamic magnocellular neurones secreting oxytocin and vasopressin. Neuroscience. 1982 Apr;7(4):773–808. doi: 10.1016/0306-4522(82)90044-6. [DOI] [PubMed] [Google Scholar]
  38. Pusch M., Neher E. Rates of diffusional exchange between small cells and a measuring patch pipette. Pflugers Arch. 1988 Feb;411(2):204–211. doi: 10.1007/BF00582316. [DOI] [PubMed] [Google Scholar]
  39. Requena J., Mullins L. J. Calcium movement in nerve fibres. Q Rev Biophys. 1979 Aug;12(3):371–460. doi: 10.1017/s0033583500005473. [DOI] [PubMed] [Google Scholar]
  40. Stuenkel E. L. Effects of membrane depolarization on intracellular calcium in single nerve terminals. Brain Res. 1990 Oct 8;529(1-2):96–101. doi: 10.1016/0006-8993(90)90815-s. [DOI] [PubMed] [Google Scholar]
  41. Stuenkel E. L., Nordmann J. J. Intracellular calcium and vasopressin release of rat isolated neurohypophysial nerve endings. J Physiol. 1993 Aug;468:335–355. doi: 10.1113/jphysiol.1993.sp019775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Stuenkel E. L., Nordmann J. J. Sodium-evoked, calcium-independent vasopressin release from rat isolated neurohypophysial nerve endings. J Physiol. 1993 Aug;468:357–378. doi: 10.1113/jphysiol.1993.sp019776. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Thayer S. A., Miller R. J. Regulation of the intracellular free calcium concentration in single rat dorsal root ganglion neurones in vitro. J Physiol. 1990 Jun;425:85–115. doi: 10.1113/jphysiol.1990.sp018094. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Turner T. J., Adams M. E., Dunlap K. Calcium channels coupled to glutamate release identified by omega-Aga-IVA. Science. 1992 Oct 9;258(5080):310–313. doi: 10.1126/science.1357749. [DOI] [PubMed] [Google Scholar]
  45. Van Eldik L. J., Zendegui J. G., Marshak D. R., Watterson D. M. Calcium-binding proteins and the molecular basis of calcium action. Int Rev Cytol. 1982;77:1–61. doi: 10.1016/s0074-7696(08)62463-8. [DOI] [PubMed] [Google Scholar]
  46. Wilson D. F. Effects of caffeine on neuromuscular transmission in the rat. Am J Physiol. 1973 Oct;225(4):862–865. doi: 10.1152/ajplegacy.1973.225.4.862. [DOI] [PubMed] [Google Scholar]
  47. Zhou Z., Neher E. Mobile and immobile calcium buffers in bovine adrenal chromaffin cells. J Physiol. 1993 Sep;469:245–273. doi: 10.1113/jphysiol.1993.sp019813. [DOI] [PMC free article] [PubMed] [Google Scholar]

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