Table 2.
Body weight (g) at 60-day interval | |||||
---|---|---|---|---|---|
Groups | Blood glucose (mmol/l) | Initial | Final | Instillation | Mean alveolar diameter (μm) |
Matching control (11) | 4.70 ± 0.17 | 221 ± 6 | 413 ± 15 | PPE | 59.65 ± 1.44‡ |
Saline | 51.50 ± 1.22 | ||||
Diabetic (7) | 28.73 ± 1.62* | 234 ± 5 | 230 ± 19* | PPE | 70.99 ± 2.34‡θδ |
Saline | 54.24 ± 1.43 | ||||
Diabetic + Insulin (7) | 19.50 ± 2.27*† | 229 ± 6 | 257 ± 4* | PPE | 61.41 ± 1.05γ |
Saline | 55.48 ± 1.59 |
Rats were rendered diabetic by the injection of alloxan (42 mg/kg, i.v.) 10 days before porcine pancreatic elastase (PPE, right lung) and saline (left lung) instillation. Diabetic rats were treated with 4 IU neutral protamine Hagedorn (NPH) insulin 2 h before instillation, followed by 2 IU/day NPH insulin for the next 50 days. Number of animals is indicated in parenthesis. Data are presented as means ± SEM and analysed by one-way anova followed by the Tukey–Kramer multiple comparisons test as follows
P < 0.001 compared with corresponding values in control group
P < 0.01 compared with values in diabetic group
P < 0.001
P < 0.01 compared with values in saline-treated lungs
P < 0.001 compared with PPE-treated lungs in control group
P < 0.01 compared with PPE-treated lungs in diabetic + insulin group.