Cellular mechanisms of cyclophosphamide-induced taste loss in mice

• Published in: PloS one 2017-09, Vol.12 (9), p.e0185473
• Main Authors: Mukherjee, Nabanita, Pal Choudhuri, Shreoshi, Delay, Rona J, Delay, Eugene R
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic Agents, Alkylating - adverse effects; Apoptosis; Appetite loss; Biology; Biology and Life Sciences; Cancer; Cancer therapies; Cell Death - drug effects; Cell growth; Cell Proliferation - drug effects; Chemotherapy; Cyclophosphamide; Cyclophosphamide - adverse effects; Cytochrome P-450; Cytotoxicity; Diet; Disturbance; Dosage and administration; Drugs; Epithelium; Histology; Life span; Lingual epithelium; Male; Malnutrition; Medicine and Health Sciences; Mice; Mice, Inbred C57BL; Peripheral neuropathy; Quality of life; Rodents; Senses; Side effects; Social Sciences; Sucrose; Sugar; Taste; Taste - drug effects; Taste buds; Taste Buds - cytology; Taste Buds - drug effects; Umami
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0185473

Many commonly prescribed chemotherapy drugs such as cyclophosphamide (CYP) have adverse side effects including disruptions in taste which can result in loss of appetite, malnutrition, poorer recovery and reduced quality of life. Previous studies in mice found evidence that CYP has a two-phase disturbance in taste behavior: a disturbance immediately following drug administration and a second which emerges several days later. In this study, we examined the processes by which CYP disturbs the taste system by examining the effects of the drug on taste buds and cells responsible for taste cell renewal using immunohistochemical assays. Data reported here suggest CYP has direct cytotoxic effects on lingual epithelium immediately following administration, causing an early loss of taste sensory cells. Types II and III cells in fungiform taste buds appear to be more susceptible to this effect than circumvallate cells. In addition, CYP disrupts the population of rapidly dividing cells in the basal layer of taste epithelium responsible for taste cell renewal, manifesting a disturbance days later. The loss of these cells temporarily retards the system's capacity to replace Type II and Type III taste sensory cells that survived the cytotoxic effects of CYP and died at the end of their natural lifespan. The timing of an immediate, direct loss of taste cells and a delayed, indirect loss without replacement of taste sensory cells are broadly congruent with previously published behavioral data reporting two periods of elevated detection thresholds for umami and sucrose stimuli. These findings suggest that chemotherapeutic disturbances in the peripheral mechanisms of the taste system may cause dietary challenges at a time when the cancer patient has significant need for well balanced, high energy nutritional intake.