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Table 1 Comparison of the chemical structure, mechanism of action, advantages and disadvantages between STZ- and alloxan-induced model

From: Diabetic retinopathy: a comprehensive update on in vivo, in vitro and ex vivo experimental models

 

Streptozotocin(STZ)

Alloxan

Source

Glucosamine–nitrosourea compound derived from Streptomyces achromogenes

Synthesised from uric acid oxidation

Mechanism of Action

Selective pancreatic β-cell uptake via GLUT2

Generates ROS

Causes DNA fragmentation

Acts as a NO donor

Generates Adenosine triphosphate (ATP) de-phosphorylation

β-cell necrotic death

Selective pancreatic β-cell uptake via the GLUT2

Inhibit glucokinase

Generates ROS

β-cell necrotic death

Advantages

Rapid simulation of natural T2DM disease progression

Induced diabetes remains longer

Cost-effective

Easy handling (stable at 37 °C within one hour)

High selective loss of pancreatic β-cell due to its inhibitory effect on glucokinase

Disadvantages

Poor standardisation

Carcinogenic to human

Can be toxic to liver and kidney cells

May cause spontaneous regeneration of β-cells

Less stable in water at room and body temperature

High variability

High mortality