My study requires the induction of STZ in 30 Sprague-Dawley rats (either sex) to develop type 2 diabetes. My protocol was:

1) Fast the rats overnight.

2) Prepared STZ solution in ice-cold citrate buffer (0.1 M, pH 4.5) and injected i.p. within 5 minutes of dissolving it. Dose used was 50 mg/kg.

3) Fed them with 10% fructose water for 24 hours post injection and gave food ad libitum.

4) Checked for blood glucose levels (BGL) 4 days after injection. Rats were fasted for 24 hours before checking the blood glucose levels.

When compared to the normal BGL, some of my rats had their BGLs around the normal fasting BGL range (4.0 - 6.5 mmol/L) while some were above 11 mmol/L.

Could there be any explanation to this? I had my supervisor's help to inject the rats as he has mastered the i.p injection technique and thus, error in the technique could be ruled out.

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