Electrical Fields: Their Nature and Influence on Biological Systems

Advanced Semiconductor and Organic Nano-Techniques

Volumn , Issue , 2003, Pages 319-346

  Colello, R J ^a   Alexander, J K ^a  

^a VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33645519876     PISSN: None     EISSN: None     Source Type: Journal    
DOI: 10.1016/B978-012507060-7/50027-1     Document Type: Article

References (88)

1. Borgens R.B., Vanable J.W., Jaffe L.F. Bioelectricity and regeneration: large currents leave the stumps of regenerating newt limbs. Proc. Natl. Acad. Sci. USA 1977, 74(10):4528.
2. Borgens R.B., Vanable J.W., Jaffe L.F. Reduction of sodium dependent stump currents disturbs urodele limb regeneration. J. Exp. Zool. 1979, 209(3):377.
3. Borgens R.B., Jaffe L.F., Cohen M.J. Large and persistent electrical currents enter the transected lamprey spinal cord. Proc. Natl. Acad. Sci. USA 1980, 77(2):1209.
4. Borgens R.B., Roederer E., Cohen M.J. Enhanced spinal cord regeneration in lamprey by applied electric fields. Science 1981, 213(4508):611.
5. Borgens R.B., McGinnis M.E., Vanable J.W., Miles E.S. Stump currents in regenerating salamanders and newts. J. Exp. Zool. 1984, 231(2):249.
6. Borgens R.B., Blight A.R., Murphy D.J., Stewart L. Transected dorsal column axons within the guinea pig spinal cord regenerate in the presence of an applied electric field. J. Comp. Neurol. 1986, 250(2):168.
7. Borgens R.B., Blight A.R., McGinnis M.E. Behavioral recovery induced by applied electric fields after spinal cord hemisection in guinea pig. Science 1987, 238(4825):366.
8. Borgens R.B., Blight A.R., McGinnis M.E. Functional recovery after spinal cord hemisection in guinea pigs: the effects of applied electric fileds. J. Comp. Neurol. 1990, 296(4):634.
9. Borgens R.B., Shi R., Mohr T.J., Jaeger C.B. Mammalian cortical astrocyte align themselves in a physiological voltage gradient. Exp. Neurol. 1994, 128:41.
10. Borgens R.B., Toombs J.P., Breur G., Widmer W.r., Waters D., Harbath A.M., March P., Adams L.G. An imposed oscillating electrical field improves the recovery of function in neurologically complete paraplegic dogs. J. Neurotrauma 1999, 16(7):639.
11. Brighton C.t., Okereke E., Pollack S.R., Clark C.C. In vitro bone-cell response to a capacitivity coupled electrical field. The role of field strength, pulse pattern, and duty cycle. Clin. Orthop. 1992, 285:255.
12. Brosenitsch T.A., Katz D.M. Physiological patterns of electrical stimulation can induce neuronal gene expression by activating N-type calcium channels. J. Neurosci. 2001, 21(8):2571.
13. Chao P.H., Roy R., Mauck R.L., Liu W., Valhmu W.B., Hung C.T. Chondrocyte translocation response to direct current electric fields. J. Biomech. Eng. 2000, 122(3):261.
14. Chen M.S., Huber A.B., van der Haar M.E., Frank M., Schnell L., Spillmann A.A., Christ F., Schwab M.E. Nogo-A is a myelin-associated neurite outgrowth inhibitor and an antigen for monoclonal antibody IN-1. Nature 2000, 403(6768):434.
15. Chenn A., McConnell S.K. Cleavage orientation and the asymmetric inheritance of Notchl immunoreactivity in mammalian neurogenesis. Cell 1995, 82(4):631.
16. Cooper M.S., Schliwa M. Electrical and ionic controls of tissue cell locomotion in DC electric fields. J. Neurosci. Res. 1985, 13(223).
17. Cork R.J., McGinnis M.E., Tsai J., Robinson K.R. The growth of PC12 neurites is biased towards the anode of an applied electrical field. J. Neurobiol. 1994, 25:1509.
18. Davies S.J., Silver J. Adult axon regeneration in adult CNS white matter. Trends Neurosci. 1998, 21(12):515.
19. Erickson C.A., Nuccitelli R. Embryonic fibroblast motility and orientation can be influenced by physiological electric fields. J. Cell Biol. 1984, 98:296.
20. Erskine L., McCaig C.D. Integrated interactions between chondroitin sulphate proteoglycans and weak dc electric field regulate nerve growth cone guidance in vitro. J. Cell. Sci. 1997, 110(Pt 16):1957.
21. Farboud B., Nuccitelli R., Schwab I.R., Isseroff R.R. DC electric fields induce rapid directional migration in cultured human corneal epithelial cells. Exp. Eye Res. 2000, 70:667.
22. Gimenez Y., Ribotta M., Privat A. biological interventions for spinal cord injury. Curr. Opin. Neurol. 1998, 11(6):647.
23. Goldman R., Pollack S. Electric fields and proliferation in a chronic wound model. bioelectromagnetics 1996, 17(6):450.
24. Grimnes s., Martinsen O.G. Bioimpedance and Bioelectricity Basics 2000, Academic Press, San Diego, CA.
25. Gruler H., Nuccitelli R. Neural crest cell galvanotaxis: new data and a novel approach to the analysis of both galvanotaxis and chemotaxis. Cell. Motil. Cytoskeleton 1991, 19(2):121.
26. Guttmann F., Keyzer H. Modern Biochemistry 1986, Plenum Press, New York.
27. Hinkle L., McCaig C.D., Robinson K.R. The direction of growth of differentiating neurones and myoblasts from frog embryos in an applied electric field. J. Physiol. 1981, 314:121.
28. Huang R., Peng L., Hertz L. Effects of a low-voltage static electric field on energy metabolism in astrocytes. Bioelectromagnetics 1997, 18(1):77.
29. Illingworth C.M. Trapped fingers and amputated finger tips in children. J. Pediatr. Surg. 1974, 9(6):853.
30. Ingvar S. Reactions of cells to the galvanic current in tissue culture. Proc. Soc. Exp. Biol. Med. 1920, 17:198.
31. Ingvar D. Experiments on the influence of electric current upon growing nerve cell processes in vitro. Acta. Physiol. Scand. 1947, 13:150.
32. Jaffe L.F. Electrical currents through the developing fucus egg. Proc. Natl. Acad. Sci. USA 1966, 56(4):1102.
33. Jaffe L.F. The role of ionic currents in establishing developmental pattern. Philos. Trans. R. Soc. Lond. B. Biol. Sci. 1981, 295(1078):553.
34. Jaffe L.F., Nuccitelli R. An ultrasensitive vibrating probe for measuring steady extracellular currents. J. Cell Biol. 1974, 63(2 Pt 1):614.
35. Jaffe L.F., Poo M.M. Neurites grow faster towards the cathode than the anode in a steady field. J. Exp. Zool. 1979, 209(1):115.
36. Jaffe L.F., Stern C.D. Strong electrical currents leave the primitive streak of chick embryos. Science 1979, 206(4418):569.
37. Jefferys J.G. Nonsynaptic modulation of neuronal activity in the brain: electric currents and extracellular ions. Physiol. Rev. 1995, 75(4):689.
38. Jenkins L.S., Duerstock B.S., Borgens R.B. Reduction of the current of injury leaving the amputation inhibits limb regeneration in the red spotted newt. Dev. Biol. 1996, 178(2):251.
39. Koryta J. Ions, Electrodes, and Membranes 1991, John Wiley and Sons, Inc., New York. 2nd edn.
40. Marsh G., Beams H.W. In vitro control of growing chick nerve fibers by applied electric currents. J. Cell. Comp. Physiol. 1946, 27:139.
41. McCaig C.D. Dynamic aspects of amphibian neurite growth and the effects of an applied electric field. J. Physiol. 1986, 375:55.
42. McCaig C.D. Electric fields, contact guidance and the direction of nerve growth. J. Embryol Exp. Morphol. 1986, 94:245.
43. McCaig C.D. Spinal neurite reabsorption and regrowth in vitro depend on the polarity of an applied electric field. Development 1987, 100(1):31.
44. McCaig C.D. Nerve guidance: a role for bio-electric fields?. Prog. Neurobiol. 1988, 30(6):449.
45. McCaig C.D. Nerve branching is induced and oriented by a small applied electric field. J. Cell Sci. 1990, 95(Pt 4):605.
46. McCaig C.D., Rajnicek A.M. Electrical fields, nerve growth and nerve regeneration. Exp. Physiol. 1991, 76(3):473.
47. McCaig C.D., Zhao M. Physiological electrical fields modify cell behaviour. BioEssay 1997, 19(9):819.
48. McCaig C.D., Sangster L., Stewart R. Neurotrophins enhance electric field-directed growth cone guidance and directed nerve branching. Dev. Dyn. 2000, 217(3):299.
49. McDevitt L., Fortner P., Pomeranz B. Application of weak electric field to the hindpaw enhances sciatic motor nerve regeneration in the adult rat. Brain Res. 1987, 416(2):308.
50. Mescher A.L. Effects on adult newt limb regeneration of partial and complete skin flaps over the amputation surface. J. Exp. Zool. 1976, 195(1):117.
51. Nuccitelli R. Endogenous ionic currents and DC electric fields in multicellular animal tissues. Bioelectromagnetics 1992, (Suppl 1):147.
52. Nuccitelli R., Jaffe L.F. Spontaneous current pulses through developing fucoid eggss. Proc. Natl. Acad. Sci. USA 1974, 71(12):4855.
53. Nuccitelli R., Smart T., Ferguson J. Protein kinases are required for embryonic neural crest cell galvanotaxis. Cell. Motil. Cytoskeleton 1993, 24(1):54.
54. Patel N., Poo M.M. Orientation of neurite growth by extracellular electric fields. J. Neurosci. 1982, 2(4):483.
55. Patel N.B., Poo M.M. Perturbation of the direction of neurite growth by pulsed and focal electric fields. J. Neurosci. 1984, 4(12):2939.
56. Peng H.B., Jaffe L.F. Polarization of fucoid eggs by steady electrical fields. Dev. Biol. 1976, 53(2):277.
57. Politis M.J., Zanakis M.F. Short term efficacy of applied electric fields in the repair of the damaged rodent spinal cord: behavioral and morphological results. Neurosurgery 1988, 23(5):582.
58. Politis M.J., Zanakis M.F. Treatment of the damaged rat hippocampus with a locally applied electric field. Exp. Brain Res. 1988, 71(1):223.
59. Politis M.J., Zanakis M.F., Albala B.J. Mammalian optic nerve regeneration following the application of electric fields. J. Trauma 1988, 28(11):1548.
60. Politis M.J., Zanakis M.F., Albala B.J. Facilitated regeneration in the rat peripheral nervous system using applied electric fields. J. Trauma 1988, 28(9):1375.
61. Pomeranz B., Campbell J.J. Weak electric current accelerates motoneuron regeneration in the sciatic nerve of ten-month-old rats. Brain Res. 1993, 603(2):271.
62. Pomeranz B., Mullen M., Markus H. Effect of applied electrical fields on sprouting of intact saphenous nerve in adult rat. Brain Res. 1984, 303(2):331.
63. Purves D., Lichtman J.W. Principles of Neural Development 1985, Sinauer Associates Inc. Publishers, Sunderland, MA.
64. Rajnicek A.M., Gow N.A., McCaig C.D. Electric field-induced orientation of rat hippocampal neurones in vitro. Exp. Physiol. 1992, 77(1):229.
65. Rajnicek A.M., Robinson K.R., McCaig C.D. The direction of neurite growth in a weak DC electric field depends on the substratum: contribution of adhesivity and net surface charge. Dev. Biol. 1998, 203:412.
66. Robinson K.R. Endogenous electrical current leaves the limb and prelimb region of the Xenopus embryo. Dev. Biol. 1983, 97(1):203.
67. Robinson K.R. The responses of cells to electrical fields: a review. J. Cell. Biol. 1985, 101(6):2023.
68. Robinson K.R., Stump R.F. Self-generated electrical currents through Xenopus neurulae. J. Physiol. 1984, 352:339.
69. Rosenspire A.J., Kindzelskii A.L., Petty H.R. Pulsed DC electric fields couple to natural NAD(P)H oscillations in HT-1080 fibrosarcoma cells. J. Cell Sci. 2001, 114(Pt 8):1515.
70. Rosenthal L.J., Reiner M.A., Bleicher M.A. Nonoperative management of distal fingertip amputations in children. Pediatrics 1979, 64(1):1.
71. Ryaby J.T. Clinical effects of electromagnetic and electric fields on fracture healing. Clin. Orthop. 1998, 355(Suppl):205.
72. Sauer H., Rahimi G., Hescheler J., Wartenberg M. Effects of electrical fields on cardiomyocyte differentiation of embryonic stem cells. J. Cell. Biochem. 1999, 75:710.
73. Schwab M.E. Regenerative nerve fiber growth in the adult central nervous system. News Physiol. Sci. 1998, 13:294.
74. Sheridan D.M., Isseroff R.R., Nuccitelli R. Imposition of a physiologic DC electric field alters the migratory response of human keratinocytes on extracellular matrix molecules. J. Invest. Dermatol. 1996, 106(4):642.
75. Silver J. Pharmacological therapy of spinal cord injury during the acute phase. Spinal Cord 2000, 38(8):505.
76. Smart I.H. Variation in the plane of cell cleavage during the process of stratification in the mouse epidermis. Br. J. Dermatol. 1970, 82(3):276.
77. Spallanzani L. Prodromo sa un Opera da Imprimersi sopra le Ripoduzion Animali. Modena 1768, 7.
78. Stewart R., Erskine L., McCaig C.D. Calcium channel subtypes and intracellular calcium stores modulate electric field-stimulated and-oriented nerve growth. Dev. Biol. 1995, 171(2):340.
79. Strome S. Determination of cleavage planes. Cell 1993, 72(1):3.
80. Wang E., Zhao M., Forrester J.V., McCaig C.D. Re-orientation and faster, directed migration of lens epithelial cells in a physiological electric field. Exp. Eye Res. 2000, 71:91.
81. Weiss P. In vitro experiments on the factors determining the course of the outgrowing nerve fiber. J. Exp. Zool. 1934, 68:393.
82. Williams S.C. A study of the reactions of growing embryonic nerve fibers to the passage of direct current through the surrouding medium. Anat. Rec. 1936, 64(Suppl 3):56.
83. Zanakis M.F. Differential effects of various electrical parameters on peripheral and central nerve regeneration. Acupunct. Electrother. Res. 1990, 15(3/4):185.
84. Zhao M., Agius-Fernandez A., Forrester J.V., McCaig C.D. Orientation and directed migration of cultured corneal epithelial cells in small electric fields are serum dependent. J. Cell Sci. 1996, 109(Pt 6):1405.
85. Zhao M., McCaig C.D., Agius-Fernandez A., Forrester J.V., Araki-Sasaki K. Human corneal epithelial cells reorient and migrate cathodally in a small applied electric field. Curr. Eye Res. 1997, 16:973.
86. Zhao M., Dick A., Forrester J.V., McCaig C.D. Electric field-directed cell motility involves up-regulated expression and asymmetric redistribution of the epidermal growth factor receptors and is enhanced by fibronectin and laminin. Mol. Biol. Cell 1999, 10(4):1259.
87. Zhao M., Forrester J.V., McCaig C.D. A small, physiological electric field orients cell division. Proc. Natl. Acad. Sci. USA 1999, 96(9):4942.
88. Zhuang H., Wang W., Seldes R.M., Tahernia A.D., Fan H., Brighton C.T. Electrical stimulation induces the level of TGF-betal mRNA in osteoblastic cells by a mechanism involving calcium/calmodulin pathway. Biochem. Biophys. Res. Commun. 1997, 237(2):225.