Plant and family Plant part used Study design Experimental findings References
Aloe arborescens; Asphodelaceae AE of leaf gel Normal and alloxan-induced diabetic rats; 21 day treatment. • Decrease FBG in diabetic rats.
• Restore plasma insulin and TAG levels.
• Increase glucokinase activity. 
[56]
Brachylaena discolor; Astaraceae DCM:MeOH (1:1) extracts of roots, leaves and stem In vitro bioassay using cultured Chang liver, 3T3-L1 adipose and C2C12 muscle cells. • Increase glucose utilization in 3T3-L1 adipocytes, Chang liver and muscle cells.   [55]
Cissampeloscapensis;
Menispermaceae
AE of leaves In vitro bioassay using cultured Chang liver, 3T3-L1 adipose and C2C12 muscle cells. • Decrease FBG level.
• No toxic effects.
[55]
Clauseriaanisata(Wild)
Hook;
Rutaceae
Root extract. Normal and STZ rats. • Cause dose dependent reduction in FBG levels. [57]
Harpagophylumprocumbens DC;
Pedaliaceae
AE of roots Normal and STZ rats. • Cause dose dependent reduction in FBG levels. [58]
Hypoxishemerocallidea(African Potato); Hypoxydaeae MeOH extract of corm and
AE of roots.
Normal and STZ rats (AT). • Cause dose dependent reduction in FBG levels.
• Less effective than glibenclamide.
[59,60]
MomordicabalsaminaL.;
Cucurbitaceae
AE of stem and flower. In vitro bioassay using cultured Chang liver, 3T3-L1 adipose and C2C12 muscle cells. • Increase glucose utilization in 3T3-L1 adipocytes, Chang liver and muscle cells.   [55]
Sclerocaryabirrea [(A. Rich) Hochst]; Anacardiaceae AE of stem bark. Normal and STZ rats (AT). • Decrease FBG levels.
• Increase plasma insulin level.
[61]
Sclerocaryabirrea [(A. Rich) Hochst]; Anacardiaceae AE of stem bark. Normal and STZ rats (AT and for 21 days treatment). • Decrease FBG levels.
• No effect on plasma insulin level.
• Increase hepatic glycogen synthesis (AT).
• Decrease plasma urea and creatinine levels.
• Increase glomerular filtrate rate.
[26]
Sclerocaryabirrea [(A. Rich) Hochst]; Anacardiaceae DCM:MeOH (1:1) extracts of stem bark and roots. In vitro bioassay using cultured Chang liver, 3T3-L1 adipose and C2C12 muscle cells. • Increase glucose utilization in the liver and muscle.
• Toxic to the hepatocytes.
[55]
Securridacalangepedunculat;
Polygalaceae
Root-bark extract. Normal and STZ rats. • Decrease FBG levels in normal and STZ rats. [52]
Vernoniaamygdalina; Compositae AE of stem Normal and STZ rats. • Increase glucose uptake. [58]
Vernoniaamygdalina; Compositae AE of leaves. Glucose uptake in rats fed with high fat diet for 8 weeks. • Normalize insulin levels.
• Increase glucose uptake in muscle and adipose tissue.
• Decrease intestinal glucose uptake.
[62]
Gongronemalatifolium; Ascepiadaceae AE of leaves. Normal and STZ rats (for 28 days treatment). • Decrease FBG levels and increase hepatic glycogen. [51,63]
Azadirachtaindica; Meliaceae AE of leaves. Normal and STZ rats (AT). • Decrease FBG levels. [64]
Vinca major L.; Apocynaceae DCM:MeOH (1:1) extracts of roots and leaves. In vitro bioassay using cultured Chang liver, 3T3-L1 adipose and C2C12 muscle cells. • Increase glucose utilization in liver.
• Cytotoxic.
[55]
AE = aqueous extract; FBG = fasting blood glucose; TAG = triacylglycerol; MeOH = methanol; CH2Cl2 = methylene chloride; STZ = streptozotocin; DCM = dichloromethane; AT = acute treatment
Table 2: Nigerian indigenous anti-diabetic medicinal plants.