Effect of extremely low frequency Electromagnetic Fields (EMF) on Phospholipase activity in the cultured cells

Korean Journal of Physiology and Pharmacology

Volumn 14, Issue 6, 2010, Pages 427-433

  Song, Ho Sun ^a   Kim, Hee Rae ^a   Ko, Myoung Soo ^a   Jeong, Jae Min ^a   Kim, Yong Ho ^a   Kim, Myung Cheul ^a   Hwang, Yeon Hee ^a   Sohn, Uy Dong ^a   Gimm, Yoon Myoung ^b   Myung, Sung Ho ^c   Sim, Sang Soo ^a  

^a Chung Ang University   (South Korea)

^b Dankook University   (South Korea)

^c Korea Electrotechnology Research Institute (KERI)   (South Korea)

Author keywords

Arachidonic acid; EMF; Phospholipase A2; Phospholipase C; Phospholipase D

Indexed keywords

ARACHIDONIC ACID; PHOSPHOLIPASE A2; PHOSPHOLIPASE C; PHOSPHOLIPASE D;

ANIMAL CELL; ARTICLE; CELL LINE; CELL MEMBRANE; CONTROLLED STUDY; ELECTROMAGNETIC FIELD; ENZYME ACTIVITY; NONHUMAN; OCCUPATIONAL EXPOSURE; SIGNAL TRANSDUCTION;

EID: 79251519315     PISSN: 12264512     EISSN: None     Source Type: Journal    
DOI: 10.4196/kjpp.2010.14.6.427     Document Type: Article

References (29)

1. Wertheimer N, Leeper E. Electrical wiring configurations and childhood cancer. Am J Epidemiol. 1979;109:273-284.
2. Floderus B, Persson T, Stenlund C, Wennberg A, Ost A, Knave B. Occupational exposure to electromagnetic fields in relation to leukemia and brain tumors: a case-control study in Sweden. Cancer Causes Control. 1993;4:465-476.
3. Matanoski GM, Elliott EA, Breysse PN, Lynberg MC. Leukemia in telephone linemen. Am J Epidemiol. 1993;137:609-619.
4. 2 enzymes: selective inhibitors and their pharmacological potential. Adv Pharmacol. 1995;32:31-66.
5. Attur MG, Patel R, Thakker G, Vyas P, Levartovsky D, Patel P, Naqvi S, Raza R, Patel K, Abramson D, Bruno G, Abramson SB, Amin AR. Differential anti-inflammatory effects of immunosuppressive drugs: cyclosporin, rapamycin and FK-506 on inducible nitric oxide synthase, nitric oxide, cyclooxygenase-2 and PGE2 production. Inflamm Res. 2000;49:20-26.
6. Petrone WF, English DK, Wong K, McCord JM. Free radicals and inflammation: superoxide-dependent activation of a neutrophil chemotactic factor in plasma. Proc Natl Acad Sci U S A. 1980;77:1159-1163.
7. 3H]inositol phosphate formation in tracheal smooth muscle. Biochem J. 1989;262:739-746.
8. Claro E, Wallace MA, Lee HM, Fain JN. Carbachol in the presence of guanosine 5′-O-(3-thiotriphosphate) stimulates the breakdown of exogenous phosphatidylinositol 4,5-bisphosphate, phosphatidylinositol 4-phosphate, and phosphatidylinositol by rat brain membranes. J Biol Chem. 1989;264:18288-18295.
9. Berridge MJ, Irvine RF. Inositol trisphosphate, a novel second messenger in cellular signal transduction. Nature. 1984;312: 315-321.
10. Somlyo AV, Bond M, Somlyo AP, Scarpa A. Inositol trisphosphate-induced calcium release and contraction in vascular smooth muscle. Proc Natl Acad Sci U S A. 1985;82:5231-5235.
11. Exton JH. Signaling through phosphatidylcholine breakdown. J Biol Chem. 1990;265:1-4.
12. Billah MM, Anthes JC. The regulation and cellular functions of phosphatidylcholine hydrolysis. Biochem J. 1990;269:281-291.
13. Nishizuka Y. Intracellular signaling by hydrolysis of phospholipids and activation of protein kinase C. Science. 1992;258: 607-614.
14. 2+-dependent phospholipase A2 enzymes. Proc Natl Acad Sci U S A. 1994;91:11060-11064.
15. 2 on arachidonic acid release Induced by reactive oxygen species. Arch of Biochem and Biophys. 2001;392:257-262.
16. 2 by bromoenol lactone and trifluoromethyl ketones. J Biol Chem. 1995;270: 445-450.
17. 2 plays a role in arachidonic acid release and eicosanoid biosynthesis by mast cells. J Immunol. 1994;152:5438-5446.
18. Dole VP, Meinertz H. Microdetermination of long-chain fatty acids in plasma and tissues. J Biol Chem. 1960;235:2595-2599.
19. 2 using pyrene-labeled phospholipids in the presence of serum albumin. Anal Biochem. 1989;177:103-109.
20. Lee CW, Park DJ, Lee KH, Kim CG, Rhee SG. Purification, molecular cloning, and sequencing of phospholipase C-beta 4. J Biol Chem. 1993;268:21318-21327.
21. Schmidt M, HÜWe SM, Fasselt B, Homann D, RÜMenapp U, Sandmann J, Jakobs KH. Mechanisms of phospholipase D stimulation by m3 muscarinic acetylcholine receptors. Eur J Biochem. 1994;225:667-675.
22. Da Silva A, Amrani Y, Trifilieff A, Landry Y. Involvement of B2 receptors in the bradykinin-induced relaxation of guinea-pig isolated trachea. Br J Pharmacol. 1995;114:103-108.
23. Lusa S, Myllarniemi M, Volmonen K, Vauhkonen M, Somerharju P. Degradation of pyrene-labelled phospholipids by lysosomal phospholipases in vitro. Dependence of degradation on the length and position of the labelled and unlabelled acyl chains. Biochemical J. 1996;315:947-952.
24. Guidelines on limits of exposure to static magnetic fields. International Commission on Non-Ionizing Radiation Protection. Health Phys. 1994;66:100-106.
25. Song HS, Park TW, Sohn UD, Shin YK, Choi BC, Kim CJ, Sim SS. The effect of caffeic acid on wound healing in skin-incised mice. Korean J Physiol Pharmacol. 2008;12:343-347.
26. 2 by methyl arachidonyl fluorophosphonate. Biochim Biophys Acta. 1996; 1302:55-60.
27. 2. Korean J Physiol Pharmacol. 2010;14:163-167.
28. Patruno A, Amerio P, Pesce M, Vianale G, Di Luzio S, Tulli A, Franceschelli S, Grilli A, Muraro R, Reale M. Extremely low frequency electromagnetic fields modulate expression of inducible nitric oxide synthase, endothelial nitric oxide synthase and cyclooxygenase-2 in the human keratinocyte cell line HaCat: potential therapeutic effects in wound healing. Br J Dermatol. 2010;162:258-266.
29. Clejan S, Ide C, Walker C, Wolf E, Corb M, Beckman B. Electromagnetic field induced changes in lipid second messengers. J Lipid Mediat Cell Signal. 1996;13:301-324.