Platelet aggregation and adenosine triphosphate (ATP) release were measured by use of the impedance method in blood samples obtained from 25 adult female Beagles before and after sedation with acepromazine (0.13 mg/kg of body weight) and atropine (0.05 mg/kg), and during general anesthesia. General anesthesia was induced by IV administration of thiamylal (average dosage, 2.1 mg/kg, range, 1.2 to 4.2 mg/kg) and was maintained with halothane in oxygen. Samples of jugular venous blood were obtained from each dog, using citrate as anticoagulant. Platelet count was done on each sample. Platelet aggregation and ATP released from the aggregating platelets were measured within 2.5 hours of sample collection, using a whole-blood aggregometer. Adenosine diphosphate (ADP) or collagen was used as aggregating agent. For each aggregating agent, platelet aggregation and ATP release were measured over 6 minutes. After sedation with acepromazine and atropine, significant (P < 0.01) reduction was observed in platelet count (from median values of 341,000 cells/microliter to 283,000 cells/microliter) and in the ability of platelets to aggregate in response to ADP (from 14.0 to 7.0 Ohms). During the same period, maximal release of ATP in response to collagen also was reduced (from 5.56 micromoles to 4.57 micromoles; P < 0.01); however, this difference ceased to be significant when ATP release was normalized for platelet count. During general anesthesia and surgery (200 minutes after sedation), platelet count and aggregation responses to ADP and collagen had returned to presedation values. None of the dogs in this study appeared to have hemostasis problems during surgery. In conclusion, sedation with acepromazine and atropine induces measurable inhibition of ADP-induced platelet aggregation that resolves during subsequent general anesthesia and surgery. Transient inhibition of platelet aggregation is not manifested by a change in gross hemostasis during surgery.

There is increasing alarm and awareness about the health dangerposed by the arthropod vector causing Onchocerciasis. This study was carried out with the aim to throw more light on the prevalence of the arthropod vector, Simulun damnosum. This research enabled us toproffer preventive advice to government and citizens. In carrying out this study, villages around flowing waters were used as sample sites. The method applied was direct observation, coupled with efficientrecording. Atmospheric temperature readings were periodically taken along with the density of the insect population observed under such temperature. The same was done for relative humidity (%), solar radiation (gm-ca/cm2, lum) and luminescence (cd/m2) in relation to the insect population of available FMH at every given period (fly per man hour). Our findings showed that climate conditions influence the reproductive level and numbers of the vector. The wet season is most conducive for the arthropod vector to reproduce and multiply. The humidity is high and temperature seems to be at the average. It is during this period that greater preventive measures need to beintentionally heightened to subdue the dangerous activities of the vector.