The L.arginine-Nitric oxide pathway has shown a role in pain felling which is a mediator with modulation effect in dorsal root of ganglionic neurons of spinal cord. The presented study goal was to clarify the influence of sex on the effects of L.arginine mediated nitric oxide on pain arbitration in both sexes of mice. The response time of hot plat test and latency period of tail flick were recorded the pain perception. The results of both groups of control and treated with L.arginine showed decrease of time response of hot plat in male than female and the same result in tail flick latency period of control group. Where as amplify of hot plat response time of male than female in L.NAME (nitric oxide synthase inhibitor) treated group. Morphine treated group were increase in all groups as compared with control. These findings might be attributed to that pain felling is intercede through diverse mediators in different sexes of mice male and female, this may possible involves sex hormone. In addition, from the result of L.NAME on pain sensation, it may be recommended that L.arginine-nitric oxide pathway is extra vital in male in comparison with female in pain sensation.

ABSTRACT 210 one day old broiler chicks were used in this study. They were divided in to two groups. The first kept on commercial diet as (control); the second group was given thiamin (vit. Bl) in dose 10 mg /bird was added to same commercial diet. Glucose concentrations, total cholesterol, total protein and the activity of the blood enzymes were determined. Results revealed a significant (p0.05) for this vitamin on the blood enzymes activity. The physiological impact of these changes were discussed.

The objective of this study was to assess the host status of the three largest southern African wild ruminants, namely giraffes, Giraffa camelopardalis, African buffaloes, Syncerus caffer, and eland, Taurotragus oryx for ixodid ticks. To this end recently acquired unpublished data are added here to already published findings on the tick burdens of these animals, and the total numbers and species of ticks recorded on 12 giraffes, 18 buffaloes and 36 eland are summarized and discussed. Twenty-eight ixodid tick species were recovered. All stages of development of ten species, namely Amblyomma hebraeum, Rhipicephalus (Boophilus) decoloratus, Haemaphysalis silacea, Ixodes pilosus group, Margaropus winthemi, Rhipicephalus appendiculatus, Rhipicephalus evertsi evertsi, Rhipicephalus glabroscutatum, Rhipicephalus maculates and Rhipicephalus muehlensi were collected. The adults of 13 species, of which the immature stages use small mammals as hosts, namely Haemaphysalis aciculifer, Hyalomma glabrum, Hyalomma marginatum rufipes, Hyalomma truncatum, Ixodes rubicundus, Rhipicephalus capensis, Rhipicephalus exophthalmos, Rhipicephalus follis, Rhipicephalus gertrudae, Rhipicephalus lounsburyi, Rhipicephalus lunulatus, Rhipicephalus pravus group and Rhipicephalus simus, were also collected.

Stabilates of Theileria parva sporozoites are mostly delivered in liquid nitrogen tanks to the East Coast fever immunization points. Using an in vitro titration model, we assessed the loss of infectivity of several stabilates when they are stored in ice baths for up to 24 h. Comparisons, with respect to rates of loss of infectivity, were made between T. parva stocks (Chitongo and Katete), cryoprotectants (sucrose and glycerol) and method of assessment (in vivo and in vitro techniques). Chitongo and Katete stabilates showed similar loss dynamics. The losses were 1-4 % (depending on parasite stock) and 3 % per hour of storage for glycerol and sucrose stabilates respectively, and the loss rates were not significantly different. The results suggest that Chitongo stabilates and sucrose cryoprotected suspensions can be delivered on ice as is done for Katete. A graphical relationship of in vitro effective dose at 50 % infectivity (ED50) and in vivo protection rate was made. The relationship showed a 35 % loss of protection for a relatively low corresponding increase of ED50 from 0.006 to 0.007 tick equivalent.

The phenogenetic and phylogenetic relationships among 7 identified strains of C. pseudotuberculosis isolated from sheep were checked by PCR specific primers demonstrated with random amplified polymorphic DNA – polymerase chain reaction (RAPD – PCR) by using five arbitrarily primers. C pseudotuberculosis isolates were distinguished according to the banding patterns of their amplified DNA on agarose gel. The variation can be used for diagnostic differentiation among C. pseudotuberculosis strains. Differences were observed in RAPD patterns between the 7 isolates and this may be due to the presence of novel serovars of this microorganism.

A cross-sectional survey of ticks infesting sheep was conducted in Sennar State, Sudan. A total body collection of ticks was carried out at five localities Sennar town, Singa, Dinder, Abu Naama and Um Banein on two types of Desert sheep (Watish and Ashgar) on two farms at each locality at two monthly intervals for one year starting July 2002 to May 2003. Four tick genera and eight species were identified. They were Amblyomma lepidum, Hyalomma anatolicum anatolicum, Hyalomma truncatum, Rhipicephalus (Boophilus) decoloratus, Rhipicephalus camicasi, Rhipicephalus evertsi evertsi, Rhipicephalus guilhoni and Rhipicephalus muhsamae. A significant (P < 0.05) seasonal pattern of activity was observed for A. lepidum and R. guilhoni with peak activity occurring during rainy seasons. The highest mean number of ticks (7.26 + 0.58) was recorded at Abu Naama, while the lowest mean (3.61 + 0.31) was recorded in Sennar. Watish type sheep carried significantly (P < 0.05) more ticks than Ashgar type.

The aim of this study was to determine withdrawal periods (WP) and tissue irritation after administration of three intramammary antibiotics [Curaclox LC (Norbrook (ARK AH)], Spectrazol Milking Cow (Schering-Plough AH) and Rilexine 200 LC [Logos Agvet (Virbac)] in goats with clinical mastitis. Withdrawal periods in goats with clinical mastitis treated with Curaclox LC, were not significantly different from those recommended for use in cows (72 h) with (67 h) or without (48 h) the 24 h mandatory safety margin while Spectrazol caused a significantly longer withdrawal period (122 h) than that recommended for use in cattle with (60 h) and without (36 h) the 24h safety margin. The withdrawal period of clinical mastitis cases treated with Rilexine 200 LC was 48 h compared to the 96 h recommended for use in cows. A linear model of regression with factors influencing the WP in goats with clinical mastitis was as follows : WP = 30.21 + 4.692 (sampling time) + 22.11 (udder pathology) - 13.6 (floccules) - 0.00649 (milk yield). Somatic Cell Counts (SCC) of milk from udder halves with clinical mastitis ranged from 7 053 x 103 to 7 948 x 103 cells per mℓ without isolations of bacteria and between 6 476 x 103 and 8 479 x 103 cells per mℓ with isolations of bacteria. Most of the variation in SCC could not be explained and the California Milk Cell Test (CMCT) and SCC on their own were not reliable methods for mastitis diagnosis. However, CMCT and SCC were indicators of udder irritation. In goats without clinical mastitis, Spectrazol Milking Cow caused the least tissue irritation followed by Rilexine 200 LC and Curaclox LC. For goats with clinical mastitis, Rilexine 200 LC caused the least irritation, followed by Curaclox LC while Spectrazol Milking Cow caused the most irritation.

Contagious bovine pleuropneumonia (CBPP), caused by Mycoplasma mycoides var. mycoides small colony (MmmSC), is one of the most important diseases of cattle in Africa. The role of innate or acquired cell mediated and humoral immunity in conferring protection against MmmSC infection has not yet been elucidated. On the other hand, the pathological lesions caused by the aetiological agent have been considered indicative of an immunopathological process. In this study ten naïve cattle were exposed to in-contact infection with animals infected by intubation with a strain of MmmSC. Clinical signs, antibody response, IFNg release and pathological changes at necropsy were analysed and compared with the events following in-contact infection of an equal number of animals kept under daily treatment with cyclosporine for the entire observation period of 84 days. Cyclosporine is a suppressor of the immune response related to the T-cell system. Under the conditions of the experiment, cyclosporine appeared to condition the pathogenesis of CBPP by delaying the events that follow infection, bringing further support to the possibility that the immune response may have an impact on the disease outcome.

A total number of 80 nasal swabs collected from apparently normal cattle slaughtered in Basateen abattoir were screened for the presence of infectious bovine rhinotracheitis virus. Among 80 examined samples, 4 samples found positive after the 3rd passage on MDBK cell line with appearance of the specific cytopathic effect (grape like clusters). The isolated virus titers were 103.9, 104.2, 105, 105.6 TCID50 / 0.1 ml. The four positive isolates were identified by agar gel precipitation test (AGPT), virus neutralization test (VNT) and gave the intracytoplasmic granules by indirect fluorescent antibody technique (IFAT). Electrophoretic profile of IBR in sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) was described and visualized by Coomassie blue stain. The mobilities of electrophoretic bands were determined with molecular weight marker at approximate range from 206.39 to 22.14 kDa.

The present study was carried out in dairy farms experiencing low reproductive efficiency. Blood samples were collected from 84 cattle and 16 buffaloes suffered from infertility problems for detection and titration of leptospiral antibodies using the microscopic agglutination test (MAT). Eleven standardized leptospira serovars were used as living antigens for this purpose. Sixteen (19.05%) and 2 (12.5%) samples were found positive for L. interrogans serovar Icterohaemorrhagiae for cattle and buffaloes respectively, with titers ≥1:200. Antibodies against L. interrogans serovar Pomona were detected in 8 (9.52%) and 2 (12.5%) in cattle and buffaloes respectively with titers ≥1:400. Two cattle (2.38%) and two buffalo (12.5%) samples were positive for L. interrogans serovar Djasiman. On the other hand, two cattle samples were positive for both L. interrogans serovar Icterohaemorrhagiae and L. interrogans serovar Pomona. Second serum samples were rechecked for seroconversion from each positively reacted animal with 3-4 weeks interval.