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1.
Indian J Med Sci ; 62(4): 141-8, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18445980

ABSTRACT

OBJECTIVES: The relationships between alpha-tocopherol, pro-oxidant and antioxidant enzyme status, and radiation toxicity were studied in stage II, III, and IVA oral squamous cell carcinoma patients. The low levels of malondialdehyde and increased activities of antioxidant enzymes were correlated with decreased oxidative stress by alpha-tocopherol in oral cancer patients treated with radiotherapy. The objective of the present study was to evaluate the effect of alpha-tocopherol on oxidant-antioxidant enzyme status in oral squamous cell carcinoma patients treated with radiotherapy. MATERIALS AND METHODS: The study included three groups with histologically confirmed oral squamous cell carcinoma patients (untreated), and they were further divided into two groups, viz., one consisting of patients who underwent radiotherapy alone (radiotherapy was given at the dosage of 6000 cGy in five fractions per week for a period of 6 weeks); and the other group treated with radiotherapy plus alpha-tocopherol supplementation (alpha-tocopherol was supplemented at a dosage of 400 IU/day) for the entire period of radiotherapy. RESULTS: A significant decrease ( P < 0.001) in malondialdehyde levels and increase in activities of antioxidant enzymes ( P < 0.001) in hemolysate were noticed in patients treated with radiotherapy and simultaneously supplemented with alpha-tocopherol when compared to radiation-treated patients. CONCLUSION: It was seen that alpha-tocopherol played a role in protecting against the damage caused by irradiation in oral squamous cell carcinoma patients treated with radiotherapy, by enhancing the antioxidant enzyme status and reducing the pro-oxidant status.


Subject(s)
Antioxidants/administration & dosage , Carcinoma, Squamous Cell/enzymology , Carcinoma, Squamous Cell/radiotherapy , Mouth Neoplasms/enzymology , Mouth Neoplasms/radiotherapy , alpha-Tocopherol/administration & dosage , Antioxidants/metabolism , Antioxidants/radiation effects , Carcinoma, Squamous Cell/drug therapy , Catalase/blood , Catalase/drug effects , Catalase/radiation effects , Female , Glucosephosphate Dehydrogenase/blood , Glucosephosphate Dehydrogenase/drug effects , Glucosephosphate Dehydrogenase/radiation effects , Glutathione Peroxidase/blood , Glutathione Peroxidase/drug effects , Glutathione Peroxidase/radiation effects , Glutathione Reductase/blood , Glutathione Reductase/drug effects , Glutathione Reductase/radiation effects , Glutathione Transferase/blood , Glutathione Transferase/drug effects , Glutathione Transferase/radiation effects , Humans , Male , Malondialdehyde/blood , Malondialdehyde/radiation effects , Middle Aged , Mouth Neoplasms/drug therapy , Reactive Oxygen Species/blood , Reactive Oxygen Species/radiation effects , Superoxide Dismutase/blood , Superoxide Dismutase/drug effects , Superoxide Dismutase/radiation effects
2.
Mol Cell Biochem ; 267(1-2): 167-76, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15663198

ABSTRACT

RP-1, a herbal preparation of Podophyllum hexandrum has already been reported to provide protection against whole body lethal gamma irradiation (10 Gy). It has also been reported to render radioprotection to germ cells during spermatogenesis. Present study was undertaken to unravel the cellular and molecular mechanism of action of RP-1 on testicular system in strain 'A' mice. Various antioxidant parameters such as thiol content, glutathione peroxidase (GPx), glutathione reductase (GR), glutathione-S-transferase (GST) enzyme activity, lipid peroxidation (LPO) and total protein levels were investigated. Thiol content was seen to increase significantly (p < 0.05) in both RP-1 alone and RP-1 pretreated irradiated groups over the irradiated groups at 8, 16 and 24 h. Irradiation (10 Gy) significantly decreased GPx, GST and GR activity in comparison to untreated control but RP-1 treatment before irradiation significantly (p < 0.05) countered radiation-induced decrease in the activity of these enzymes. Radiation-induced LPO was also found to be reduced at all time intervals by RP-1 treatment before irradiation. As compared to irradiated group the protein content in testicular tissue was increased in RP-1 pretreated irradiated group at 4 and 16 h significantly (p < 0.05). Comets revealed by single-cell gel electrophoresis were significantly longer (p < 0.001) in irradiated mice than in unirradiated control. RP-1 treatment before irradiation, however, rendered significant increase (p < 0.05) in comet length over the corresponding control and irradiated group initially at 4 h but at later time points, this was reduced significantly (p < 0.01) as compared to the irradiated group. RP-1 treatment alone rendered shorter comets at 8, 16 and 24 h than irradiated groups (p < 0.001). This study implies that RP-1 offers radioprotection at biochemical and cytogenetic level by protecting antioxidant enzymes, reducing LPO and increasing thiol content.


Subject(s)
Plant Extracts/pharmacology , Podophyllum , Radiation-Protective Agents/pharmacology , Spermatogenesis/radiation effects , Whole-Body Irradiation , Animals , Comet Assay , Gamma Rays , Glutathione Peroxidase/radiation effects , Glutathione Reductase/radiation effects , Glutathione Transferase/radiation effects , Lipid Peroxidation/radiation effects , Male , Mice , Mice, Inbred A , Phytotherapy , Plant Extracts/therapeutic use , Plants, Medicinal , Proteins/analysis , Proteins/radiation effects , Sulfhydryl Compounds/radiation effects , Time Factors
3.
J Formos Med Assoc ; 102(7): 486-91, 2003 Jul.
Article in English | MEDLINE | ID: mdl-14517587

ABSTRACT

BACKGROUND AND PURPOSE: Both infrared and low-power laser have been applied to improve circulation, wound repair, and pain control. Infrared and low-power laser therapies have the potential for stimulating enzyme activities which might contribute to increased glutathione (GSH) concentration and provide protection against oxidative damage. This study investigated cell viability, and GSH and its related enzyme activities in rat hepatocytes after irradiation. METHODS: Hepatocytes were isolated from 8-week-old male Sprague-Dawley rats and the cultures were divided into infrared, laser, and control groups. The cells were treated with infrared and low-power laser at a distance of 35 cm for 20 minutes. The cell morphology, lactate dehydrogenase (LDH) leakage, lipid peroxidation, GSH concentration, GSH peroxidase, GSH reductase (GRd), and GSH S-transferase activities were measured after irradiation. RESULTS: The morphology and LDH leakage of hepatocytes in the irradiation groups did not differ significantly from those of the control group. After infrared irradiation, a significant decrease in thiobarbituric acid-reactive substances and an increase in GSH concentration were found after 48 hours of incubation compared to the control group (p < 0.05). Furthermore, laser irradiation resulted in a significant increase in GRd activity after 48 hours of incubation compared to the control group (p < 0.05). A 48-hour incubation period produced greater GRd activity in all groups compared to a 24-hour period (p < 0.05). CONCLUSIONS: Irradiation did not damage rat hepatocytes in this study. Infrared was shown to stimulate GSH production, while laser irradiation increased GRd activity.


Subject(s)
Cell Survival/radiation effects , Glutathione/radiation effects , Infrared Rays , Liver/radiation effects , Low-Level Light Therapy , Analysis of Variance , Animals , Cells, Cultured , Glutathione/metabolism , Glutathione Peroxidase/metabolism , Glutathione Peroxidase/radiation effects , Glutathione Reductase/metabolism , Glutathione Reductase/radiation effects , Glutathione Transferase/metabolism , Glutathione Transferase/radiation effects , L-Lactate Dehydrogenase/metabolism , L-Lactate Dehydrogenase/radiation effects , Lipid Peroxidation , Liver/cytology , Liver/enzymology , Rats , Rats, Sprague-Dawley
4.
Arch. argent. dermatol ; 53(4): 147-157, jul.-ago. 2003. ilus
Article in Spanish | LILACS | ID: lil-383793

ABSTRACT

Las formulaciones disponibles actualmente para uso dermatológico, basadas en sustancias antioxidantes tales como vitaminas C y E, entre otras, abundan con promesas de revertir el envejecimiento cutáneo. En el presente trabajo se realiza una revisión de los sistemas antioxidantes cutáneos, de la relación entre envejecimiento y daño oxidativo, así como de la evidencia disponible en cuanto al tratamiento con antioxidantes. La intención de este artículo es que el dermatólogo comprenda las bases fisiológicas de acción de los antioxidantes, para poder juzgar su utilidad con una mirada crítica


Subject(s)
Humans , Animals , Ascorbic Acid/therapeutic use , Antioxidants , Reactive Oxygen Species , Skin , Skin Aging , Ultraviolet Rays , Vitamin E , Ascorbic Acid/pharmacology , Ascorbic Acid/physiology , Administration, Topical , Antioxidants , beta Carotene , Catalase , Clinical Trials as Topic , Cosmetics , Skin Physiological Phenomena , Glutathione Peroxidase/radiation effects , Glutathione Peroxidase/physiology , Glutathione Reductase/radiation effects , Glutathione Reductase/physiology , Glutathione Transferase/radiation effects , Glutathione Transferase/physiology , Interleukins , Ozone , Peroxidase , Skin , Sunlight , Superoxide Dismutase/radiation effects , Superoxide Dismutase/physiology , Ubiquinone , Vitamin E
5.
Arch. argent. dermatol ; 53(4): 147-157, jul.-ago. 2003. ilus
Article in Spanish | BINACIS | ID: bin-4186

ABSTRACT

Las formulaciones disponibles actualmente para uso dermatológico, basadas en sustancias antioxidantes tales como vitaminas C y E, entre otras, abundan con promesas de revertir el envejecimiento cutáneo. En el presente trabajo se realiza una revisión de los sistemas antioxidantes cutáneos, de la relación entre envejecimiento y daño oxidativo, así como de la evidencia disponible en cuanto al tratamiento con antioxidantes. La intención de este artículo es que el dermatólogo comprenda las bases fisiológicas de acción de los antioxidantes, para poder juzgar su utilidad con una mirada crítica (AU)


Subject(s)
Humans , Animals , Skin Aging , Antioxidants/physiology , Ascorbic Acid/therapeutic use , Vitamin E/therapeutic use , Skin/radiation effects , Reactive Oxygen Species , Ultraviolet Rays/adverse effects , Antioxidants/therapeutic use , Antioxidants/radiation effects , Ascorbic Acid/pharmacology , Ascorbic Acid/physiology , Vitamin E/pharmacology , Vitamin E/physiology , Skin/drug effects , Skin Physiological Phenomena , Superoxide Dismutase/physiology , Superoxide Dismutase/radiation effects , Catalase/physiology , Catalase/radiation effects , Peroxidase/physiology , Peroxidase/radiation effects , Glutathione Peroxidase/physiology , Glutathione Peroxidase/radiation effects , Glutathione Reductase/physiology , Glutathione Reductase/radiation effects , Glutathione Transferase/physiology , Glutathione Transferase/radiation effects , beta Carotene/physiology , beta Carotene/radiation effects , Ubiquinone/physiology , Ubiquinone/radiation effects , Ozone/adverse effects , Administration, Topical , Cosmetics , Clinical Trials as Topic , Interleukins/radiation effects , Sunlight/adverse effects
6.
J Photochem Photobiol B ; 55(2-3): 113-9, 2000.
Article in English | MEDLINE | ID: mdl-10942075

ABSTRACT

Supplementation of human mononuclear cells with 3 and 6 mM of lipoic acid produces an inhibition of the antioxidant adaptive response triggered by treatment with UV-B light (0.30 W/m2 for 15 min). Supplementation with 1.5 mM of lipoic acid gives no conclusive results. The adaptive response is characterized by an increase in the activities of superoxide dismutase, catalase, glutathione peroxidase and DT-diaphorase. Catalase (5.5 +/- 0.6 pmol/mg prot) increases its activity by up to 22 +/- 3 pmol/mg prot, after irradiation with UV-B. Supplementation with 3 and 6 mM of lipoic acid completely inhibits the adaptive response. The activities of the membrane-bound mitochondrial enzymes succinate dehydrogenase and cytochrome oxidase do not increase after UV-B exposure. Moreover, their activities are found to decrease and the addition of lipoic acid does not prevent this effect. The inhibition of the antioxidant response by lipoic acid in human cells appears as indirect evidence of the existence of oxidative stress in the development of this response. As lipoic acid behaves as an effective antioxidant, it seems that its action decreases the intracellular oxidative signals necessary to develop the adaptive response in human mononuclear cells.


Subject(s)
Catalase/blood , Glutathione Peroxidase/blood , Leukocytes, Mononuclear/drug effects , Leukocytes, Mononuclear/radiation effects , Superoxide Dismutase/blood , Thioctic Acid/pharmacology , Ultraviolet Rays , Adult , Catalase/radiation effects , Cell Survival/drug effects , Cell Survival/radiation effects , Dihydrolipoamide Dehydrogenase/blood , Dihydrolipoamide Dehydrogenase/radiation effects , Female , Glutathione Peroxidase/radiation effects , Humans , In Vitro Techniques , Leukocytes, Mononuclear/enzymology , Male , Superoxide Dismutase/radiation effects
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