BACKGROUND: The protozoancryptosporidiumisan important intestinal parasitic infection in domestic ruminants that has the potential for transmission between humans and livestock throughout the world and Iran. OBJECTIVES: The present study was undertaken to determine cryptosporidiuminfection in different age groupsof cattle and water buffaloesin farms of Mahabad suburb, Iran. METHODS: For this purpose, a total number of 248 fresh fecal samples were randomly collected from rectum of cattle and water buffaloesin farms of 4 villages from May2016 to May 2017. The fecal samples were subjected to floatation technique andcryptosporidiumoocysts were collected using Sucrose Gradient and Percole flotation technique and stained with modified Ziehl-Neelsen technique. RESULTS: Overall prevalence of cryptosporidiuminfection was 50% (124/248). The highest rate of infection was significant in female calves (30.65%) less than one year-old. The highest infection rate was significantly found in summer (20.16%). Cryptosporidium parvum and C. andersoni were identified in 40.32% (100/248) and 9.68% (24/248) of examined cattle, respectively. Mixed infection was 8.47%. CONCLUSIONS: The results of this study indicated that C.parvum was prevalent in cattle of the region, therefore, further molecular studies are recommended to determine the genotypes of the parasiteas a potential zoonotic agent.

The ameliorative effect of salts, ascorbic acid olyphosphate and zinc oxide supplementation on heat stress was studied in adult buffaloes of either sex which were randomly divided into two groups of four animals each. Group I served as control and Group II was supplemented with sodium bicarbonate, potassium carbonate, ascorbic acid polyphosphate and zinc oxide. All the animals were exposed to two conditions of temperature and humidity: hot-dry and hot-humid in psychrometric chamber for 4 hours daily for 10 days. Blood was collected on days 1, 5 and 10 of treatment. The activities of enzymes catalase, superoxide dismutase (SOD) and concentrations of reduced glutathione (GSH), hormone cortisol and thiobarbituric acid (TBA) binding substances (lipid peroxidation) were estimated in serum. Significant decreasewas observed in activities of serum catalase and SOD. Serum GSH concentration decreased while serum concentrations of TBA binding substances and cortisol significantly increased in both groups which were subjected to heat stress. Dietary supplementation of ascorbate, zinc and electrolytes resulted in further decrease in the enzymes' activities where as the serum GSH increased at par to normal values. Serum concentrations ofTBA binding substances and cortisol were comparatively lower in supplemented group in both types of stress. Thus, supplementation of ascorbate and zinc in addition to electrolytes relieved the animals of oxidative stress.

Different segments of oviduct (infundibulum, ampulla, isthmus and utero tubaljunction)of six buffaloes each during follicular and luteal phases of estrous cycle were studied. The samples were collected in 10% NBF processed for paraffin sectioning were stained with hematoxylin and eosin, Masson's trichrome, PetiodicAcid Schiff, alcian blue and PASalcian blue. The mucosa was found thrown into longitudinal folds having primary, secondary and tertiary branches. Branching was more pronounced in infundibulum and ampulla as well as during the follicular phase as compared to luteal phase. The different segments were lined with columnarto pseudostratifiedcolumnarepithelium.The cellswere ciliatedand non ciliated type. In follicular phase, the epithelium showed strong PASreaction which was con~entrated in the supranuclear zone while during the luteal phase the reaction was moderate. The reaction was granular in nature. The epithelium was also strongly positive for alcian blue and PASalcian blue during follicularphase. Thepropria submucosa, tunica muscularis and tunica serosa showed weak to mild reaction for PASand alcian blue.

The objective of this study was to evaluate cost-effective intervention for enhanced fertility in buffaloes, which could otherwise remain un-bred for variable long time. A total of 165 postpartum anestrus buffaloes were examined gynaeco-clinically at farmer's door. The animals identified with corpus luteum in either of the ovary, were treated with 500 £gg of Cloprostenol, single injection or double injection at 11 days interval (Gr. I). The remaining animals with smooth and inactive ovaries were randomly divided in three different groups. The group II animals were injected 100-150 mg progesterone for successive 5 days and single injection of 500 I.U. of PMSG on seventh day. The animals of group III were administered with 20 £gg of GnRH analogue and 7 days later, with 500 _Ýg of Cloprostenol. A second injection of 10 £gg GnRH analogue was given after 48 hrs of Cloprostenol injection. Group IV animals received 50 gm mineral mixture daily for 30 days along with 30 Nutrisacc boli (1 bolus b.i.d. for 15 days). The proportion of animals that exhibited estrus were 89.13, 86.84, 82.35 and 59.57% and the mean treatment-estrus intervals were 3.97¡Ó0.46, 4.38¡Ó0.49, 3.08¡Ó0.23 and 21.78¡Ó2.56 days in group I, II, III and IV, respectively. The animals detected in estrus were bred by natural service using fertile bulls and diagnosed for pregnancy per rectum 50 days post service. The first service conception rate was 46.34, 33.33, 53.57 and 28.57 % in-group I, II, III and IV, respectively, while the overall conception rate was significantly higher (78.57%) in GnRH-treated animals. The cost of treatment in different groups was Rs. 160 or 320, 220, 525 and 150, respectively. The results indicate that better fertility in postpartum anestrus buffaloes can be obtained by GnRH therapy though; the cost of intervention seems to be higher than other treatments.

The buffalo calves became ataxic at 6.16±1.07 minute of acepromazine administration. There was good sedation. The animals stood up with ataxia at 131.5±17.80 minute and complete recovery took 211.83±6.94 minutes. Significant hypotension and tachycardia were observed after acepromazine administration. Midazolam caused ataxia at 3.33±0.76 minute and animals went into sternal recumbency at 34.0±15.85 minute. There was good muscle relaxation. Complete recovery took 183.5±10.92 minutes. Significant increase in respiratory rate was observed at the its peak effect. A significant reduction in mean arterial pressure (MAP) was also seen at 30 minute of midazolam administration. Diazepam produced ataxia within one minute and animals went into sternal recumbency. It produced quick onset of action and delayed recovery. A significant hypotension was observed at 5 minute of diazepam with decreased pulse pressure. No change was observed in electrocardiograph on administration of acepromazine and diazepam but slight increase in the amplitude of primary T-wave was observed after midazolam administration.