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. 2020 Mar 9;10:4362. doi: 10.1038/s41598-020-60947-x

Figure 2.

Figure 2

Implanted islet-seeded biomaterial into diabetic mice reduces glucose levels. Islet-seeded biomaterial or respective controls were injected intraperitoneal into both STZ-induced and NOD diabetic mice. STZ-induced diabetic mice were treated with biomaterial-only (n = 7), islets-only (n = 6) or islet-seeded biomaterial (n = 8). Days −25 through 0 designate pre-treatment period to identify baseline glucose levels. STZ was injected day −7 through day −3 (for a total of 5 days) to induce diabetes. (A) STZ-induced diabetic mice assessment of blood glucose levels recorded over the treatment time period. Dashed horizontal line represents 16.7 nmol/L marker for diabetes determination. (B) Glucose tolerance test (GTT) performed in STZ-induced diabetic mice on day 20 post-implantation treatment with islets-only, biomaterial-only or islet-seeded biomaterial. (C) Total blood insulin levels were measured 120 min after GTT performed in STZ-induced diabetic mice 20 days post-implantation treatment. (D) NOD diabetic groups were treated with biomaterial-only (n = 6), islet-only (n = 6) or islet-seeded biomaterial (n = 8). Blood glucose levels recorded over 30 days post-implantation. (E) GTT performed in NOD treated mice on day 20 post-implantation. (F) Total blood insulin levels measured after GTT performed in NOD treated groups on day 20 post-implantation. Paired student t test was utilized for statistical analysis. A p value < 0.05 was considered statistically significant; * is p < 0.05, ** is p <0.01 and ns = not significant. Error bars for all figures indicate standard errors of the mean (SEM).