Abstract
Many survivors of childhood cancer experience significant side effects leading to inferior quality of life like chemotherapy-induced cognitive impairment (CICI). A growing body of literature implies that the gut-brain axis modulates neurological and inflammatory physiology. Cancer therapy may alter the gut microbiome in ways that modify the risk of CICI. We utilized a commonly used pediatric cancer chemotherapy drug, doxorubicin (DOXO), in our juvenile rat model, including both male and female rats. At 5 weeks of age, Long Evans rats were treated with weekly intraperitoneal DOXO (2 mg/kg/dose for 4 weeks). Compared to PBS-treated rats, DOXO treatment caused impairment of visual memory among female rats and spatial memory among male rats, when tested 3-4 weeks after DOXO exposure. In both sexes, DOXO-induced cognitive deficits do not persist among the surviving animals. Microbiome analyses were conducted in fecal samples collected 48 hours following the final DOXO injection. Compared to PBS-treated rats, female DOXO-treated rats had significant differences in beta diversity. Significant changes in the abundances of specific species, genera, and phyla were observed. These experimental results set the stage for further investigations of how chemotherapy-induced changes in gut microbiome might contribute to CICI, and point toward therapeutic interventions.