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Hot infusion of Nyctanthes arbo-tristis Linn. (Oleaceae) flowers are used often by some elderly Sri Lankan Buddhist monks as a potential sedative. However, in Ayurvedic, traditional and folkloric medicine of Sri Lanka, no such implication has been made regarding therapeutic activity of these flowers. The aim of this study was to investigate the sedative potential of N. arbo-tristis flowers in rats using the hole-board technique. A hot flower infusion was made as used by the monks in different concentrations (3.7, 7.5, 12.5, or 18.7 mg=kg) and was orally administered. Sedative potential was assessed 2 h posttreatment. The infusion had a moderate dose-dependent conscious sedative activity in male but, surprisingly, not in female rats. The infusion was well tolerated (in terms of overt toxic signs, liver or kidney functions) even following subchronic treatments and also did not show any overt signs of dependence (classical signs of withdrawal reactions). Sedation appears to result mainly by antioxidant, membrane stabilizing, and by yet undiscovered mechanisms of sedative actions of anthocyanin, a flavonoid, in the flower.

According to Sri Lankan traditional medicine, a decoction made from stems and leaves of Anisomeles indica Kuntze (Lamiaceae) possesses analgesic activity. However, the validity of this claim has not been scientifically tested. The aim of this study was to investigate analgesic and antihyperalgesic activities of this plant using a water extract made from the leaves and stems. The water extracts were made from leaves and stems of both preflowering (E1) and flowering plants (E2). E1 showed a dose-dependent analgesic effect up to 6 h of treatment when tested in rats using the hot plate and the tail flick techniques. Further, the analgesic effect of E1 was not accompanied by toxic effects. This effect was neither gender dependent nor dependent on the stage of the estrous cycle. E1 also showed a dose-dependent antihyperalgesic activity in the hot plate test. In contrast, E2 did not show any analgesic effect (500 mg/kg). The analgesic effect produced by E1 was not abolished by naloxone. E1 dose-dependently retarded the amplitude of the spontaneous contractions of isolated dioestrous rat uterus. Further, E1 induced a dosedependent plasma membrane stabilisation effect on rat erythrocytes. Collectively, these observations suggest that the analgesic and antihyperalgesic effects of E1 are mediated from inhibition of COX-1, thus impairing the synthesis of prostaglandins. A change in chemical contents that accompanies flowering could be one possible reason for the inability of E2 to demonstrate analgesic effect.

Recently, sodium nitroprusside (SNP), a potent nitric oxide (NO) donor and a clinically used antihypertensive, has been introduced as a penile self-injection medical therapy for erectile dysfunction. However, it is known that many antihypertensives impairs sexual competence; NO regulates sexual competence and NO is cytostatic and cytotoxic for human sperm. Thus, a possibility exists that SNP may impair male reproductive competence. Testing this aspect is the aim of this study. This was assessed in male rats (using three I.P. doses: 60, 30 or 20 g/kg) using noncompetitive copulation tests. The results show that the highest dose of SNP was toxic and caused rapid mortality of treated rats (within 30 min). The mid and low doses of SNP reversibly impaired several parameters of sexual competence in a dose-related fashion: sexual arousability, libido and sexual vigour. Some parameters of sexual behaviour remained unaltered: sexual motivation and intromission ratio, whilst one parameter was improved: sexual performance. In complete contrast, the ejaculatory competence and fertility remained unchanged. The SNP-induced impairments in sexual competence may be attributable to lowered testosterone levels and sedation mediated via its specific action and/or side effect. Further, this impairment of sexual function was not due to general toxicity, inhibition of penile sensitivity, penile erection or analgesic activity. It is concluded that SNP impairs male sexual competence, at least, in rats although it promotes penile erection.