The possible effect of Croton zambesicus administration on vital organs has been less investigated despite its extensive traditional use in tropical Africa. We therefore aim at elucidating the effect of ethanolic extract on the testes. The aqueous fraction of ethanolic leaf extract of C. zambesicus (5 and 10 mg/Kg body weight) was administered to verify its effect on sperm concentration, sperm motility, sperm progessivity, malondialdehyde and catalase activities for a period of five consecutive days. The result showed that there is a significant increase in sperm production, sperm motility and sperm progressivity in the treated group when compared with the control; while there was a reduction in malondialdehyde and catalase activity in all the treated groups. The slight increase in the weight of the measured parameters also indicated the positive effect of the extract in the normal metabolic activities in the treated groups. This investigation has shown that the leaf extract possesses promising profertility property which can be exploited in fertility therapy.

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1. The effects of artemether (12.5, 25.0 and 50.0 mg/kg per day, i.m.), administered to different groups of Plasmodium berghei-infected and -uninfected adult Wistar rats for 1 week, were investigated. 2. The parameters evaluated were the feeding, drinking and urinating patterns of the rats and these were compared with those of rats that received normal saline. 3. Artemether caused a significant dose-dependent reduction in food consumption of both P. berghei-infected and -uninfected rats (P < 0.05). Food intake in infected rats was reduced by approximately 7 g/24 h. This reduction in food intake was further reduced during drug treatment with artemether. Artermether also reduced food intake in uninfected rats. The food consumption of rats that received 12.5 and 25.0 mg/kg artemether was restored after stopping treatment, in contrast with rats that received 50.0 mg/kg, in which the significant reduction in food consumption persisted 1 week after drug administration. 4. During treatment with artemether, the water intake of infected rats was significantly lower than that of uninfected rats in the 12.5 mg/kg artemether-treated group, but was significantly higher in infected rats than in uninfected rats dosed with 25.0 and 50.0 mg/kg artemether. 5. For all doses of artemether tested, a significant increase in urine output was observed in infected rats during treatment and 1 week after treatment, whereas in uninfected rats a significant increase in urine output was observed only following 25.0 and 50.0 mg/kg artemether 1 week after drug administration. 6. The present study confirms the anorexic activity of a high dose of artemether in both P. berghei-infected and -uninfected rats. It also indicates that high doses of the drug could cause impaired renal function in rats and that the significant increase in urine output could also be due to other effects of artemether, namely those on thirst, anti-diuretic hormone output and the osmotic pressure of the blood.

The consumption of Silkworm, Anaphe venata has been reported to be associated with a high incidence of seasonal ataxia in some parts of Nigeria. Injection of some doses of Aqueous Anaphe venata extract (AAV) by intraperitoneal route into mice has been reported to cause some behavioral changes associated with ataxia. We administered some doses of the extract (50-300 mg/kg) to mice orally in view of finding its effects on their fecal pellet output and elucidating the mechanism of action of the extract in the intestine of the mice. The extract caused a significant increase in fecal pellet weight and intestinal transit which was not dose-dependent. Doses of 200 and 300 mg/kg of the extract caused more significant reversal of loperamide-induced constipation than castor oil. Chlorpheniramine nifedipine and promethazine (1 mg/kg) blocked the increased fecal pellet output induced by the extract, while atropine and hexamethonium (1 mg/kg) did not block this effect of the extract. We concluded that AAV increased fecal pellet output of mice by increasing the peristaltic waves in their intestine via stimulation of H 1 receptors and opening of L-type calcium channels and not through the cholinergic receptors.

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