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NIS - libdoc.who.int - World Health Organization

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WHO monographs on medicinal plants commonly used in the Newly Independent States (<strong>NIS</strong>)<br />

than in the control rats (p < 0.01). Creatinine clearance in the treated<br />

diabetic rats was significantly lower than in the non-treated diabetic rats<br />

(p < 0.05). There was no significant difference in urinary albumin excretion<br />

between non-treated diabetic rats and treated diabetic rats. It was concluded<br />

that a water extract of the style of Zea mays prevented glomerular hyperfiltration<br />

and suppressed the progression of diabetic glomerular sclerosis in<br />

rats with streptozocin-induced diabetes (66).<br />

Haematological effects<br />

A methanol extract of dried styles expressed strong platelet aggregationinhibiting<br />

activity with a median inhibitory concentration (IC 50<br />

) of 0.3 µg/<br />

ml by adenosine diphosphate (ADP), collagen, and arachidonic acid-induced<br />

platelet aggregation. The ethyl acetate extract of dried styles inhibited<br />

platelet aggregation induced by arachidonic acid (IC 50<br />

= 0.2 mg/ml),<br />

collagen (IC 50<br />

= 0.2 mg/ml), ADP (IC 50<br />

= 0.5 mg/ml), and platelet aggregating<br />

factor (IC 50<br />

= 0.7 mg/ml) (67, 68). In cell culture, a chloroform extract<br />

of the dried stigmas of Zea mays inhibited the tumour necrosis factor-alpha<br />

(TNFα)-induced adhesion of endothelial cells to monocytic<br />

cells with a median effective dose (ED 50<br />

) of 70 µg/ml. Similar results were<br />

reported for bacterial lipopolysaccharide-induced cell adhesion with an<br />

ED 50<br />

of 82 µg/ml. The results obtained were significant at the p < 0.01 level.<br />

A 100% ethanol extract of the stigmas of Zea mays has also been reported<br />

to possess <strong>int</strong>ercellular cell adhesion molecule-1-inhibitory activity<br />

against bacterial lipopolysaccharide-induced <strong>int</strong>ercellular cell adhesion<br />

molecule-1-expression with an ED 50<br />

of 50 µg/ml. The same effect with an<br />

ED 50<br />

of 38 µg/ml was detected in an EAHY926 cell culture against TNFαinduced<br />

<strong>int</strong>ercellular cell adhesion molecule-1-expression (69).<br />

Haemodynamic effects<br />

A hot aqueous extract of fresh stigmas produced a negative chronotropic<br />

and hypotensive effect in dogs anaesthetized with pentobarbital for up to<br />

80 seconds by <strong>int</strong>ravenous injection at a dose of 1.37–22 mg/kg (70). An<br />

aqueous-ethanol (1:1) extract of fresh styles (five parts of fresh plant material<br />

in 100 parts of water/ethanol) administered by gastric <strong>int</strong>ubation to<br />

conscious rats at a dose of 40 ml/kg had a hypotensive effect (71).<br />

Antibacterial, anticrustacean and anti-complementary activity<br />

A 100% (non-diluted) ethanol extract of shade-dried stigmas of Zea mays<br />

(concentration 2.5 mg/disc) inhibited the growth of Staphylococcus aureus<br />

and Candida albicans in vitro, and exhibited an anticrustacean activity<br />

against Artemia salina (median lethal dose, 128 µg/ml) (72). A hot aque-<br />

430

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