Fractionated Irradiation and Early Changes in Noradrenaline Induced Potassium Efflux (⁸⁶Rb⁺) in Rat Parotid Gland

References

• Altman K L, Gerber G B, Okada S. Interphase death: Radiation induced death. Radiation biochemistry, G B Gerber, S Okada. Academic Press Inc., New York 1970; 246–60
   Google Scholar
• Stephens L C, Ang K K, Schultheiss T E, King G K, Brock W A, Peters L J. Target cell and mode radiation injury in Rhesus salivary glands. Radiother Oncol 1986; 7: 165–74
   PubMed Web of Science ®Google Scholar
• Stephens L C, King G K, Peters L J, Ang K K, Schultheiss T E, Jardine J H. Acute and late radiation injury in Rhesus monkey parotid glands. Evidence of interphase cell death. Am J Pathol 1986; 124: 469–78
   PubMed Web of Science ®Google Scholar
• Andersson M, Henriksson R, Domellof L, Sundstrom S. Neither 5-fluorouracil nor 5′-deoxy-5-fluorouridine involves direct interaction with neuroregulated processes. Cancer Ther Control 1989; 1: 67–73
   Google Scholar
• Danielsson Å, Henriksson R, Sundström S, Wester P. Dopamine actions in vitro on enzyme and electrolyte secretion from normal and sympathetomized rat parotid glands. J Physiol 1988; 404: 145–56
   PubMed Web of Science ®Google Scholar
• Alper T. The role of membrane damage in radiation induced cell death. Adv Exp Med Biol 1977; 84: 139–65
   PubMedGoogle Scholar
• Henriksson R. β1- and β2-adrenoceptor agonists have different effects on rat parotid cells. Am J Physiol 1982; 242: G481–5
   Google Scholar
• Östman M, Sundström S, Reiz S, Henriksson R. Isoflurane — A study of its adrenoreceptor interaction in the isolated rat parotid gland. Anesthesiology 1986; 64: 734–8
   PubMed Web of Science ®Google Scholar
• Emellin N. Nervous control of mammalian salvary glands. Philos Trans R Soc Lond ‘Biol’ 1981; 296: 27–35
   PubMed Web of Science ®Google Scholar
• Butcher F R, Putney J W. Regulation of parotid gland function by cyclic nucleotides and calcium. Adv Cyclic Nucleotide Res 1980; 13: 15–249
   Google Scholar
• Butcher F R, Goldman J A, Nemerovski M. Effect of adrenergic agents on amylase release and adenosine-3′,5′-monophosphate accumulation in rat parotid slices. Biochem Biophys Acta 1975; 392: 82–94
   PubMed Web of Science ®Google Scholar
• Carlsöö B, Danielsson Å, Henriksson R, Idahl L Å. Characterization of the rat parotid β-adrenoceptor. Br J Pharmacol 1981; 72: 271–6
   PubMed Web of Science ®Google Scholar
• Sundström S, Danielsson Å, Henriksson R, Lindström P. Characterization of dopamine-induced potassium efflux in rat parotid acinar cells. Eur J Pharmacol 1988; 145: 123–31
   PubMed Web of Science ®Google Scholar
• Sundström S, Henriksson R, Lindström P. Dopamine increases potassium efflux in rat parotid gland by stimulating noradrenaline release from sympathetic nerve endings. Brain Res 1985; 337: 155–8
   PubMed Web of Science ®Google Scholar
• Lange C S, Gilbert C W. Studies on the cellular basis of radiation lethality. III. The measurement of stem-cell repopulation probability. Int J Radiat Biol 1968; 4: 373–88
   Google Scholar
• Moore J V, Hendry J H, Hunter R D. Dose-incidence curves for tumor control and normal tissue injury, in relation to response of clonogenic cells. Radiother Oncol 1983; 1: 143–57
   PubMedGoogle Scholar
• Thames H D, Hendry J H. Fractionation in radiotherapy. Taylor Francis. 1987; 53–59; 166–9
   Google Scholar
• Desai I D, Sawant P L, Tappel A L. Peroxidative and radiation damage to isolated lysosomes. Biochem Biophys Acta 1964; 86: 277–85
   PubMed Web of Science ®Google Scholar
• Wills E D, Wilkinson A E. Release of enzymes from lysosomes by irradiation and the realtion of lipid peroxide formation to enzyme release. Biochem J 1966; 99: 657–66
   PubMed Web of Science ®Google Scholar
• Putney J W. Biphasic modulation of potassium release in rat parotid gland by carbachol and phenylephrine. J Pharmacol Exp Ther 1976; 198: 375–84
   PubMed Web of Science ®Google Scholar
• Petersen O H. Calcium-activated potassium channels and fluid secretion by exocrine glands. Am J Physiol 1986; 251: G1–13
   Google Scholar
• Merrick T P, Bruce A K. Radiation response of potassium efflux. In: Micrococcus radiodurans and sacrina lutea. Radiat Res 1965; 24: 612–8
   PubMed Web of Science ®Google Scholar
• Shapiro B, Kollman G, Asnen J. Mechanism of the effect of ionizing radiation on sodium uptake by human erythrocytes. Radiat Res 1966; 27: 139–58
   Web of Science ®Google Scholar
• Sutherland R M, Stannard J N, Weed R I. Involvement of sulphi groups in radiation damage to the human erythrocyte membrane. Int J Radiat Biol 1967; 12: 551–64
   Web of Science ®Google Scholar
• Dowben R M, Zuckerman L. Alterations in skeletal muscle after X-irradiation and their similarity to changes in muscular dystrophy. Nature 1963; 197: 400–1
   Web of Science ®Google Scholar
• Henriksson R, Bjermer L, von Shoultz E, Grankvist K. The effects of estramustine cytotoxicity on microtubuli is different from the effects of free oxygen radicals on DNA and cell membrane. Anticancer Res 1990; 10: 303–10
   PubMed Web of Science ®Google Scholar
• Farber J L, El Mofty S K. The biochemical pathology of liver cell neurosis. Am J Pathol 1975; 81: 237–50
   PubMed Web of Science ®Google Scholar
• El Mofty S K, Kahn S K, Kahn A J. Early membrane injury in lethaly irradiated salivary gland cells. Int J Radiat Biol 1981; 39: 55–62
   Web of Science ®Google Scholar
• Hicks M, Gebicki J M. A quantitative relationship between permeability and the degree of peroxidation in ufasome membranes. Biochem Biophys Res commun 1978; 80: 704–8
   PubMed Web of Science ®Google Scholar
• Casarett A P. Chap 8, 9. Radiation biology. Prentise Hall Inc, Englewood Cliffs, New Jersey 1968
   Google Scholar
• Putney J W. Muscarinic, alpha-adrenergic and peptide receptors regulate the same calcium influx sites in the parotid gland. J Physiol 1977; 268: 139–49
   PubMed Web of Science ®Google Scholar
• Eidus L K, Korystov N, Dobrovinskaya O R, Shaposhnikova. The mechanism of radiation-induced interphase death of lymphoid cells: A new hypothesis. Radiat Res 1991; 123: 17–21
   Web of Science ®Google Scholar
• Broval Ch, Schacter B. Radiation sensitivity of human natural killer cell activity: Control by X-linked genes. J. Immunol. 1981; 126: 2236–9
   PubMed Web of Science ®Google Scholar