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1.
Clin. transl. oncol. (Print) ; 19(11): 1329-1336, nov. 2017. ilus, graf
Article in English | IBECS | ID: ibc-167114

ABSTRACT

Purpose. Radiation-induced oral mucositis is the most common side effect of radiotherapy in head and neck cancer; however, effective modalities for its prevention have not been established. In this study, we evaluated the effectiveness of Hangeshashinto (TJ-14), a Japanese herbal medicine, for preventing radiation-induced mucositis and elucidated its effect on inflammatory responses, including inflammatory cell chemotaxis and cyclooxygenase-2 (COX2) expression, in an animal model. Methods. Syrian hamsters, 8–9 weeks old, were enrolled in this study. Animals were irradiated with a single 40 Gy dose to the buccal mucosa. Hamsters freely received a treatment diet mixed with 2% TJ-14 or a normal diet daily. The therapeutic effect was determined based on the visual mucositis score, body weight, and histological examination of infiltrated neutrophils and COX2 expression. Results. TJ-14 significantly reduced the severity of mucositis. The percentage with severe mucositis (score ≥3) was 100% in the untreated group and 16.7% in the TJ-14 group (P < 0.05). There was no difference in body weight change between the groups; however, weight gain in the untreated group tended to be suppressed compared to that in the TJ-14 group during the peak period of mucositis. In addition, TJ-14 inhibited the infiltration of neutrophils and COX2 expression in irradiated mucosa (P < 0.05). Conclusions. TJ-14 reduced the severity of mucositis in an animal model by suppressing the inflammatory response. Because TJ-14 is inexpensive and its safety is established, it is a promising candidate for the standard treatment of radiation-induced mucositis in cancer patients (AU)


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Subject(s)
Animals , Mucositis/drug therapy , Mucositis/radiotherapy , Cyclooxygenase 2/analysis , Drugs, Chinese Herbal/administration & dosage , Drugs, Chinese Herbal/therapeutic use , Chemotaxis/radiation effects , Mucositis/veterinary , Models, Animal , Radiotherapy/adverse effects , Radiotherapy/veterinary , Inflammation/complications , Inflammation/veterinary
2.
Clin Transl Oncol ; 19(11): 1329-1336, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28516399

ABSTRACT

PURPOSE: Radiation-induced oral mucositis is the most common side effect of radiotherapy in head and neck cancer; however, effective modalities for its prevention have not been established. In this study, we evaluated the effectiveness of Hangeshashinto (TJ-14), a Japanese herbal medicine, for preventing radiation-induced mucositis and elucidated its effect on inflammatory responses, including inflammatory cell chemotaxis and cyclooxygenase-2 (COX2) expression, in an animal model. METHODS: Syrian hamsters, 8-9 weeks old, were enrolled in this study. Animals were irradiated with a single 40 Gy dose to the buccal mucosa. Hamsters freely received a treatment diet mixed with 2% TJ-14 or a normal diet daily. The therapeutic effect was determined based on the visual mucositis score, body weight, and histological examination of infiltrated neutrophils and COX2 expression. RESULTS: TJ-14 significantly reduced the severity of mucositis. The percentage with severe mucositis (score ≥3) was 100% in the untreated group and 16.7% in the TJ-14 group (P < 0.05). There was no difference in body weight change between the groups; however, weight gain in the untreated group tended to be suppressed compared to that in the TJ-14 group during the peak period of mucositis. In addition, TJ-14 inhibited the infiltration of neutrophils and COX2 expression in irradiated mucosa (P < 0.05). CONCLUSIONS: TJ-14 reduced the severity of mucositis in an animal model by suppressing the inflammatory response. Because TJ-14 is inexpensive and its safety is established, it is a promising candidate for the standard treatment of radiation-induced mucositis in cancer patients.


Subject(s)
Chemotaxis/drug effects , Cyclooxygenase 2/chemistry , Drugs, Chinese Herbal/therapeutic use , Gamma Rays/adverse effects , Inflammation/drug therapy , Mucositis/drug therapy , Radiation Injuries, Experimental/prevention & control , Animals , Cells, Cultured , Cricetinae , Disease Models, Animal , Female , Inflammation/etiology , Inflammation/pathology , Mesocricetus , Mouth Mucosa/metabolism , Mouth Mucosa/pathology , Mouth Mucosa/radiation effects , Mucositis/etiology , Mucositis/pathology
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