Nerve growth factor and brain-derived neurotrophic factor attenuate angiotensin-II-induced facilitation of calcium channels in acutely dissociated nucleus tractus solitarii neurons of the rat

Archives of Oral Biology

Volumn 53, Issue 12, 2008, Pages 1192-1201

  Endoh, Takayuki ^a   Sato, Daisuke ^a   Wada, Yoshiyuki ^a   Ishihara, Kazuyuki ^a   Hashimoto, Sadamitsu ^a   Yoshinari, Masao ^a   Matsuzaka, Kenichi ^a   Tazaki, Masakazu ^a   Inoue, Takashi ^a  

^a TOKYO DENTAL COLLEGE   (Japan)

Author keywords

Angiotensin II; Brain derived neurotrophic factor; Nerve growth factor; Voltage dependent Ca2+ channel current

Indexed keywords

ANGIOTENSIN II; BRAIN DERIVED NEUROTROPHIC FACTOR; CALCIUM CHANNEL; NERVE GROWTH FACTOR; VASOCONSTRICTOR AGENT;

ANIMAL; ARTICLE; CALCIUM SIGNALING; DRUG EFFECT; PATCH CLAMP; PHYSIOLOGY; RAT; SOLITARY TRACT NUCLEUS; WISTAR RAT;

ANGIOTENSIN II; ANIMALS; BRAIN-DERIVED NEUROTROPHIC FACTOR; CALCIUM CHANNELS; CALCIUM SIGNALING; NERVE GROWTH FACTOR; PATCH-CLAMP TECHNIQUES; RATS; RATS, WISTAR; SOLITARY NUCLEUS; VASOCONSTRICTOR AGENTS;

RATTUS;

EID: 53549126967     PISSN: 00039969     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.archoralbio.2008.07.006     Document Type: Article

References (59)

1. Levi-Montalcini R., and Angeletti P.U. Nerve growth factor. Physiol Rev 48 (1968) 534-569
2. Thoenen H., Bandtlow C., and Heumann R. The physiological function of nerve growth factor in the central nervous system: comparison with the periphery. Rev Physiol Biochem Pharmacol 109 (1987) 145-178
3. Davies A.M. The neurotrophic hypothesis: where does it stand?. Phil Trans R Soc Lond B Biol Sci 351 (1996) 389-394
4. Stoll M., Stechelings U.M., Paul M., Bottari S.P., Metzger R., and Unger T. The angiotensin AT2-receptor mediates inhibition of cell proliferation in coronary endothelial cells. J Clin Invest 95 (1995) 651-657
5. Tsuzuki S., Eguchi S., and Inagami T. Inhibition of cell proliferation and activation of protein tyrosine phosphatase mediated by angiotensin II type 2 (AT2) receptor in R3T3 cells. Biochem Biophys Res Commun 228 (1996) 825-830
6. Laflamme L., Gasparo M., Gallo J.M., Payet M.D., and Gallo-Payet N. Angiotensin II induction of neurite outgrowth by AT2 receptors in NG108-15 cells. Effect counteracted by the AT1 receptors. J Biol Chem 271 (1996) 22729-22735
7. Meffert S., Stoll M., Steckelings U.M., Bottari S.P., and Unger T. The angiotensin II AT2 receptor inhibits proliferation and promotes differentiation in PC12W cells. Mol Cell Endocrinol 122 (1996) 59-67
8. Tsien R.W., Lipscombe D., Madison D.V., Bley K.R., and Fox A.P. Multiple types of neuronal calcium channels and their selective modulation. Trends Neurosci 11 (1988) 431-438
9. Sheng M., and Greenberg M.E. The regulation and function of c-fos and other immediate early genes in the nervous system. Neuron 4 (1990) 477-485
10. Spitzer N.C., Gu X., and Olson E. Action potentials, calcium transients and the control of differentiation of excitable cells. Curr Opin Neurobiol 4 (1994) 70-77
11. 2+-dependent regulation in neuronal gene expression. Curr Opin Neurobiol 7 (1997) 419-429
12. Nicotera P., and Orrenius S. The role of calcium in apoptosis. Cell Calcium 23 (1998) 173-180
13. Marshall J., Dolan B.M., Garcia E.P., Sathe S., Tang X., Mao Z., and Blair L.A. Calcium channel and NMDA receptor activities differentially regulate nuclear C/EBPβ levels to control neuronal survival. Neuron 39 (2003) 625-639
14. Weick J.P., Groth R.D., Isaksen A.L., and Mermelstein P.G. Interaction with PDZ proteins are required for L-type calcium channels to activate cAMP response element-binding protein-dependent gene expression. J Neurosci 23 (2003) 3446-3456
15. 2+ channels and their role in modulation of neuroendocrine cell proliferation and death. Cell Calcium 35 (2004) 307-315
16. 2+ regulation and gene expression in normal brain aging. Trends Neurosci 27 (2004) 614-620
17. Jean A. Brain stem control of swallowing: neuronal network and cellular mechanisms. Physiol Rev 81 (2001) 929-969
18. Lawrence A., and Jarrott B. Neurochemical modulation of cardiovascular control in the nucleus tractus solitarius. Prog Neurobiol 48 (1996) 21-53
19. Paton J.F.R. The Sharpey-Schafer prize lecture. Nucleus tractus solitarii: integrating structures. Exp Physiol 84 (1999) 815-833
20. Wang G., Anrather J., Huang J., Speth R.C., Pickel V.M., and Iadecola C. NADPH oxidase contributes to angiotensin II signaling in the nucleus tractus solitarius. J Neurosci 24 (2004) 5516-5524
21. 2+, and protein kinase C play a role in angiotensin II-induced free radical production in nucleus tractus solitarius. Hypertension 48 (2006) 482-489
22. Endoh T. Involvement of src tyrosine kinase and mitogen-activated protein kinase in the facilitation of calcium channels in rat nucleus of the tractus solitarius by angiotensin II. J Physiol 568 (2005) 851-865
23. Rhim H., and Miller R. Opioid receptors modulate diverse types of calcium channels in the nucleus tractus solitarius of the rat. J Neurosci 14 (1994) 7608-7615
24. Hamill O.P., Marty A., Neher E., Sakmann B., and Sigworth F.J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch 391 (1981) 85-100
25. Endoh T. Modulation of voltage-dependent calcium channels by neurotransmitters and neuropeptides in parasympathetic submandibular ganglion neurons. Arch Oral Biol 49 (2004) 539-557
26. Casaccia-Bonnefil P., Gu C., Khursigara G., and Chao M.V. p75 neurotrophin receptor as a modulator of survival and death decisions. Microsc Res Tech 45 (1999) 217-224
27. Barbacid M. The Trk family of neurotrophin receptors. J Neurobiol 25 (1994) 1386-1403
28. Berg M.M., Sternberg D.W., Parada L.F., and Chao M.V. K-252a inhibits nerve growth factor-induced trk proto-oncogene tyrosine phosphorylation and kinase activity. J Biol Chem 267 (1992) 13-16
29. Endoh T. Pharmacological characterization of inhibitory effects of postsynaptic opioid- and cannabinoid-receptors on calcium currents in neonatal rat nucleus tractus solitarius. Br J Pharmacol 147 (2006) 391-401
30. Rogers M., and Hendry I. Involvement of dihydropyridine-sensitive calcium channels in nerve growth factor-dependent neurite outgrowth by sympathetic neurons. J Neurosci Res 26 (1990) 447-454
31. Cheng B., McMahon D.G., and Mattson M.P. Modulation of calcium current, intracellular calcium levels and cell survival by glucose deprivation and growth factors in hippocampal neurons. Brain Res 607 (1993) 275-285
32. Piiper A., and Zeuzem S. Receptor tyrosine kinases are signaling intermediates of G protein-coupled receptors. Curr Pharm Des 10 (2004) 3539-3545
33. Arthur D.B., Akassoglou K., and Insel P.A. P2Y2 and TrkA receptors interact with Src family kinase for neuronal differentiation. Biochem Biophys Res Commun 347 (2006) 678-682
34. Ehlers M.D., Kaplan D.R., Price D.L., and Koliatsos V.E. NGF-stimulated retrograde transport of trkA in the mammalian nervous system. J Cell Biol 130 (1995) 149-156
35. Tsui-Pierchala B.A., and Ginty D.D. Characterization of an NGF-P-TrkA retrograde-signaling complex and age-dependent regulation of TrkA phosphorylation in sympathetic neurons. J Neurosci 19 (1999) 8207-8218
36. Delcroix J.D., Valletta J.S., Wu C., Hunt S.J., Kowal A.S., and Mobley W.C. NGF signaling in sensory neurons: evidence that endosomes carry NGF retrograde signals. Neuron 39 (2003) 69-84
37. Ye H., Kuruvilla R., Zweifel L.S., and Ginty D.D. Evidence in support of signaling endosome-based retrograde survival of sympathetic neurons. Neuron 39 (2003) 57-68
38. Gomez-Pinilla F., Ying Z., Roy R.R., Molteni R., and Edgerton V.R. Voluntary exercise induces a BDNF-mediated mechanism that promotes neuroplasticity. J Neurophysiol 88 (2002) 2187-2195
39. 1 receptor: gain-of-function study using gene transfer. Proc Natl Acad Sci USA 92 (1995) 10663-10667
40. Yamada T., Horiuchi M., and Dzau V. Angiotensin II type 2 receptor mediates programmed cell death. Proc Natl Acad Sci USA 93 (1996) 156-160
41. Kumar S., Boehm J., and Lee J.C. p38 MAP kinases: key signaling molecules as therapeutic targets for inflammatory diseases. Nat Rev Drug Discov 2 (2003) 717-726
42. Ji R.R. Peripheral and central mechanisms of inflammatory pain, with emphasis on MAP kinases. Curr Drug Targets Inflamm Allergy 3 (2004) 299-303
43. Saklatvala J. The p38 MAP kinases pathway as a therapeutic target in inflammatory disease. Curr Opin Pharmacol 4 (2004) 372-377
44. + channels in hippocampus involves a mitogen-activated protein kinase pathway. J Neurosci 22 (2006) 4860-4868
45. Sweatt J.D. Mitogen-activated protein kinases in synaptic plasticity and memory. Curr Opin Neurobiol 14 (2004) 311-317
46. Endoh T. Characterization of modulatory effects of postsynaptic metabotropic glutamate receptors on calcium currents in rat nucleus tractus solitarius. Brain Res 1024 (2004) 212-224
47. Chao M.V. Neurotrophins and their receptors: a convergence point for many signaling pathways. Nat Rev Neurosci 4 (2003) 299-309
48. Kalb R. The protean of neurotrophins and their receptors on the life and death of neurons. Trends Neurosci 28 (2005) 5-11
49. Hefti F., Hartikka J., Eckenstein F., Gnahn H., Heumann R., and Schwab M. Nerve growth factor increases choline acetyltransferase but not survival or fiber outgrowth of cultured fetal septal cholinergic neurons. Neuroscience 14 (1985) 55-68
50. Hefti F. Nerve growth factor promotes survival of septal cholinergic neurons after fimbrial transactions. J Neurosci 6 (1986) 2155-2162
51. Friedman W.J., Ibanez C.F., Hallbook F., Persson H., Cain L.D., Dreyfus C.F., et al. Differential actions of neurotrophins in the locus coeruleus and basal forebrain. Exp Neurol 119 (1993) 72-78
52. Impey S., Obrietan K., and Storm D.R. Making new connections: role of ERK/MAP kinase signaling in neuronal plasticity. Neuron 23 (1999) 11-14
53. Culmsee C., Gerling N., Lehmann M., Nikolova-karakashian M., Prehn J.H.M., Mattson M.P., et al. Nerve growth factor survival signaling in cultured hippocampal neurons is mediated through TrkA and requires the common neurotrophin receptor p75. Neuroscience 115 (2002) 1089-1108
54. Shen K.F., and Crain S.M. Nerve growth factor rapidly prolongs the action potential of mature sensory ganglion neurons in culture, and this effect requires activation of Gs-coupled excitatory kappa-opioid receptors on these cells. J Neurosci 14 (1994) 5570-5579
55. Kafitz K.W., Rose C.R., Thoenen H., and Konnerth A. Neurotrophin-evoked rapid excitation through Trk-B receptors. Nature 401 (1999) 918-921
56. Levine E.S., Dreyfus C.F., Black I.B., and Plummer M.R. Differential effects of NGF and BDNF on voltage-gated calcium currents in embryonic basal forebrain neurons. J Neurosci 15 (1995) 3084-3091
57. 2+ spikes and waves in embryonic neurons: signaling systems for differentiation. Trend Neurosci 17 (1994) 115-118
58. 2+ channels can transiently potentiate excitatory synaptic transmission in the hippocampus. Neuron 9 (1992) 1175-1183
59. Bading H., Ginty D.D., and Greenberg M.E. Regulation of gene expression in hipocampal neurons by distinct calcium signaling pathways. Science 260 (1993) 181-186