The Stable Nitroxide Tempol Facilitates Salivary Gland Protection during Head and Neck Irradiation in a Mouse Model

Purpose: Radiotherapy is commonly used to treat a majority of patients with head and neck cancers. The long-term radiation-induced reduction of saliva output significantly contributes to the posttreatment morbidity experienced by these patients. The purpose of this study was to test the ability of the stable-free radical Tempol (4-hydroxy-2,2,6,6-tetramethylpiperidine-N-oxyl), an established radioprotector, to prevent radiation-induced salivary hypofunction in mice. Experimental Design: The heads of C3H mice were exposed to a range of single radiation doses with or without an i.p. injection of 275 mg/kg Tempol 10 min before treatment. Salivary gland output was assessed 8 weeks postirradiation. Results: Radiation caused a dose-dependent reduction in salivary flow in this model. Tempol treatment alone significantly reduced radiation-induced salivary hypofunction. The combination of Tempol with mouth/nose shielding showed essentially complete radiation protection at 15 Gy and ∼75% protection at 17.5 Gy. Conclusions: This study demonstrates for the first time that significant radioprotection of the salivary glands is possible with Tempol in C3H mice.

[1]  J. Greenberger,et al.  Mitochondrial Localization of Superoxide Dismutase is Required for Decreasing Radiation-Induced Cellular Damage , 2003, Radiation research.

[2]  L. Dawson,et al.  Salivary Gland Sparing and Improved Target Irradiation by Conformal and Intensity Modulated Irradiation of Head and Neck Cancer , 2003, World Journal of Surgery.

[3]  D. Brizel,et al.  Does amifostine have a role in chemoradiation treatment? , 2003, The Lancet. Oncology.

[4]  A. Vissink,et al.  Prevention and treatment of the consequences of head and neck radiotherapy. , 2003, Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists.

[5]  I. Saito,et al.  Possible Role of Nitric Oxide in Radiation-Induced Salivary Gland Dysfunction , 2003, Radiation research.

[6]  S. Terakawa,et al.  Secretion of Saliva in X-Irradiated Rat Submandibular Glands , 2003, Radiation research.

[7]  R. Nagler,et al.  Prophylactic treatment reduces the severity of xerostomia following radiation therapy for oral cavity cancer. , 2003, Archives of otolaryngology--head & neck surgery.

[8]  James B. Mitchell,et al.  Differential protection by nitroxides and hydroxylamines to radiation-induced and metal ion-catalyzed oxidative damage. , 2002, Biochimica et biophysica acta.

[9]  G. R. Davies,et al.  An investigation into the use of pilocarpine as a sialagogue in patients with radiation induced xerostomia. , 2002, Australian dental journal.

[10]  B. Baum,et al.  The use of gene transfer for the protection and repair of salivary glands. , 2002, Oral diseases.

[11]  M I Koukourakis,et al.  Amifostine in clinical oncology: current use and future applications , 2002, Anti-cancer drugs.

[12]  H. Sugiya,et al.  Understanding salivary fluid and protein secretion. , 2002, Oral diseases.

[13]  J. Ebersole,et al.  Measuring short-term gamma-irradiation effects on mouse salivary gland function using a new saliva collection device. , 2001, Archives of oral biology.

[14]  Zvi Fuks,et al.  Endothelial Apoptosis as the Primary Lesion Initiating Intestinal Radiation Damage in Mice , 2001, Science.

[15]  L. Dawson,et al.  Xerostomia and its predictors following parotid-sparing irradiation of head-and-neck cancer. , 2001, International journal of radiation oncology, biology, physics.

[16]  Taylor Murray,et al.  Cancer Statistics, 2001 , 2001, CA: a cancer journal for clinicians.

[17]  B. Vikram,et al.  Phase III randomized trial of amifostine as a radioprotector in head and neck cancer. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[18]  James B. Mitchell,et al.  Radiation, Radicals, and Images , 2000, Annals of the New York Academy of Sciences.

[19]  A. Vissink,et al.  Radiation induced cell loss in rat submandibular gland and its relation to gland function. , 2000, International journal of radiation biology.

[20]  S. Yamano,et al.  Salivary gland cytokine expression in NOD and normal BALB/c mice. , 1999, Clinical immunology.

[21]  I. Ambudkar,et al.  Radiation-induced progressive decrease in fluid secretion in rat submandibular glands is related to decreased acinar volume and not impaired calcium signaling. , 1999, Radiation research.

[22]  P. Fox,et al.  Long-term salivary effects of single-dose head and neck irradiation in the rat. , 1998, Archives of oral biology.

[23]  R. Coppes,et al.  Radiation-induced apoptosis in relation to acute impairment of rat salivary gland function. , 1998, International journal of radiation biology.

[24]  A. Vissink,et al.  Sialogogue-related radioprotection of salivary gland function: the degranulation concept revisited. , 1997, Radiation research.

[25]  J. C. Roberts,et al.  Radiation protection by alpha-methyl-homocysteine thiolactone in vitro. , 1997, Life sciences.

[26]  S. Hahn,et al.  Evaluation of tempol radioprotection in a murine tumor model. , 1997, Free radical biology & medicine.

[27]  D. Coffin,et al.  Protection from radiation-induced alopecia with topical application of nitroxides: fractionated studies. , 1996, The cancer journal from Scientific American.

[28]  P. Fox,et al.  A 2 week pair-fed study of early X-irradiation effects on rat major salivary gland function. , 1996, Archives of oral biology.

[29]  P. Fox,et al.  Effects of X irradiation on the function of rat salivary glands at 3 and 40 days. , 1993, Radiation research.

[30]  P. Fox,et al.  Acute effects of X irradiation on the function of rat salivary glands. , 1993, Radiation research.

[31]  D. Longo,et al.  Overexpression of mitochondrial manganese superoxide dismutase promotes the survival of tumor cells exposed to interleukin‐1, tumor necrosis factor, selected anticancer drugs, and ionizing radiation , 1993, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[32]  S. Hahn,et al.  Identification of nitroxide radioprotectors. , 1992, Radiation research.

[33]  D. Grahame,et al.  Oxoammonium cation intermediate in the nitroxide-catalyzed dismutation of superoxide. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[34]  S. Hahn,et al.  Tempol, a stable free radical, is a novel murine radiation protector. , 1992, Cancer research.

[35]  A. Vissink,et al.  Acute irradiation effects on morphology and function of rat submandibular glands. , 1991, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

[36]  S. Hahn,et al.  Inhibition of oxygen-dependent radiation-induced damage by the nitroxide superoxide dismutase mimic, tempol. , 1991, Archives of biochemistry and biophysics.

[37]  James B. Mitchell,et al.  Biologically active metal-independent superoxide dismutase mimics. , 1990, Biochemistry.

[38]  P. Riesz,et al.  A novel metal-free low molecular weight superoxide dismutase mimic. , 1988, The Journal of biological chemistry.

[39]  C. Sonntag,et al.  The chemical basis of radiation biology , 1987 .

[40]  T. Morton,et al.  Radioprotection by WR-2721 of gamma-irradiated rat parotid gland: effect on gland weight and secretion at 8-10 days post irradiation. , 1984, International journal of radiation oncology, biology, physics.

[41]  J. Yuhas Efficacy testing of WR-2721 in Great Britain everything is black and white at the gray lab. , 1983, International journal of radiation oncology, biology, physics.

[42]  A. Cairnie Adverse effects of radioprotector WR2721. , 1983, Radiation research.

[43]  F. Stewart,et al.  Radioprotection of two mouse tumors by WR-2721 in single and fractionated treatments. , 1983, International journal of radiation oncology, biology, physics.

[44]  J. Yuhas,et al.  The role of WR-2721 in radiotherapy and/or chemotherapy. , 1980, Cancer clinical trials.

[45]  A. D. Conger,et al.  Radioprotection by WR-2721 against long-term chronic damage to the rat parotid gland. , 1978, Radiation research.

[46]  A. D. Conger,et al.  Short-term radioprotective effects of WR-2721 on the rat parotid glands. , 1978, Radiation research.

[47]  J. Yuhas,et al.  Differential chemoprotection of normal and malignant tissues. , 1969, Journal of the National Cancer Institute.