Haematology and serum chemistry was studied in young (5-6 months) and adult (2-2½ years) changthangi goats (Capra hircus) to investigate the age associated changes in blood constituents. Significant difference was recorded in most of the haematological and biochemical indices between two age groups. Higher values were recorded for total erythrocytes (16.63 ± 0.61 and 12.79 ± 0.56 x 106 / cumm) in young and adult respectively when compared to reference values for goats which speaks of its adaptation to high altitude hypoxic conditions. The total leukocyte count (9.99 ± 0.72 x 103/ cumm) in young was significantly (P0.01) higher as compared to the adults (6.38 ± 0.65 x 103/ cumm). Present study has shown significant (P0.01) age related difference in differential leukocyte count, with neutrophils high in young and lymphocytes in adults. Biochemical studies revealed age associated difference with total proteins (7.48 ± 0.08 g/ dl), cholesterol (108.40 ± 6.26 mg/ dl), triglycerides (99.20 ± 7.79 mg/dl), LDL (20. 20 ± 2.01mg/dl), HDL (68.14 ± 3.65mg/ dl) and creatinine (0.92 ± 0.04 mg/ dl) higher in adults and enzymes like ALP (151.31 ± 10.26 u/l) and AST (165.43 ± 4.7 u/l) higher in young. The study indicated that age be considered while interpreting the clinical and experimental data.

This study aimed to evaluate a system that identifies cartilage turn over and/or degradation through measurement of a new keratan sulfate (KS) epitope concentration in equine sera. Blood samples were collected from 30 horses, 1 (n=15) and 2 year-olds (n=15). Serum samples were analyzed for an epitope of keratan sulfate by 1/20/5D4 (KS5D4) and new epitopes of keratan sulfate using high sensitive keratan sulfate (HSKS), measured by two respective enzyme-linked immunosorbant assays (ELISAs). There was no correlation in serum concentration of KS evaluated using 5D4 and HSKS. Age had no significant effect on concentrations of KS measured with KS5D4 while 1 year-old horses showed significantly higher amounts than 2 year-olds with HSKS. Results suggest that HSKS could detect early signs of cartilage metabolic changes.

Bone marrow derived mesenchymal stem cells (MSCs) can be used to repair articular cartilage defects, these cells should be properly stimulated so that they could differentiate morphologically and hold cellular synthetic features closer to maturely differentiated chondrocytes. It is well known that tissue specific environment plays an important role in cell fate determination. Once improved isolation, proliferation and differentiation protocols have been developed, the likelihood of spontaneous differentiation of MSCs into divergent lineages will be reduced, thus increasing their value for cartilage repair. The purpose of this study was to improve chondrogenic differentiation of equine MSCs using coculture with mature equine articular chondrocytes (ACs), along with the determination of the effect of adding transforming growth factor (TGF) beta1 in the pellet culture system. Following confirmation of multilineage (adipogenic, osteogenic and chondrogenic) differentiation, isolated MSCs, ACs and coculture of both cell types were transferred into pellet culture system in a DMEM-based medium supplemented with or without TGFbetal. Chondrogenic differentiation was evaluated histologically and the relative mRNA expressions of collagen type 1 alpha1 (COL1A1), collagen type 2 alpha1 (COL2A1), aggrecan (ACAN) and SRY-box 9 (SOX9) were estimated by quantitative RT-PCR. Cocultured cells showed diffuse distribution of extracellular matrix (ECM), whereas in chondrocyte pellets it was more localized to central regions. Expression of COL2A1, ACAN and SOX9 genes were higher in cocultured pellets when compared to MSCs and ACs-composed pellets. Addition of TGFbeta1 in chondrogenic differentiating medium did not consistently amplify expression of the above mentioned genes. Differentiation of equine MSCs was enhanced by coculturing in association with mature ACs, improving expression of cartilage-specific genes and producing a more homogeneous production of ECM within the newly formed cocultured cartilage. The use of the coculture system could possibly enhance the capacity of MSC-derived chondrocytes to build up stable articular cartilage-like constructs, which could play an important role in articular cartilage repair and regeneration.

The present study characterizes canine reticulocyte exosomes. Exosomes are small membrane vesicles involved in membrane remodeling that are released from reticulocytes during the final maturation step of red blood cells. The vesicles collected from reticulocyte culture supernatants by differential centrifugation contained major exosomal proteins including heat shock protein cognate 70 (Hsc70) and transferrin receptors (TfR), consistent with the definition of the exosome. In addition, the Na,K-ATPase alpha-subunit and stomatin, a lipid raft-associated protein, were extruded by the exosome pathway, possibly leading to the absence of these proteins in erythrocytes, while the major protein constituents of erythrocyte membranes, spectrin and band 3 were retained in reticulocytes and not expelled into exosomes. The Na,K-ATPase alpha-subunit, as well as TfR and about half of the stomatin contained in exosomes, was obtained in a detergent-soluble fraction that was distinct from the lipid raft micro domain. Moreover, Na,K-ATPase and a portion of stomatin were distributed differently to Hsc70, TfR, stomatin, and ganglioside Gsub(M1) in vesicles separated with sucrose density gradient centrifugation. These results demonstrate that a heterogeneous group of exosomes participates in the loss of Na,K-ATPase and membrane remodeling during reticulocyte maturation in dogs.

The hooded phenotype is one of the coat color phenotype seen peculiarly in the rat. The hooded locus showing autosomal recessive inheritance is mapped to chromosome (Chr) 14 and that the hooded phenotype receives modification by hooded-modifier gene showing the linkage to the hooded locus. However, a gene responsible for either the hooded or hooded-modifier gene is not yet identified. To clarify genetic control of hooded phenotype, we carried out genetic linkage studies using BN and LEA rats. For determination of phenotypic variation, we measured ratio of pigmented coat area in parental and their Fsub(1) and Fsub(2) rats. We, then, conducted a genome-wide scan on 152 Fsub(2) rats for linkage with ratio of pigmented coat area for the dorsal, ventral and total regions. A major quantitative trait locus (QTL), D14Got40, showing highly significant linkage contributing 70-90% of the variance for hooded phenotype was detected on Chr 14, which may be correspondent to the hooded locus. In addition, another QTL, D17Rat2, showing highly significant linkage was also detected on Chr 17 in dorsal region phenotype as well as a QTL showing suggestive linkage on Chr15 in ventral region phenotype. We, further, investigated a genome-wide scan for epistatic interactions and detected significant interactions between D14Got40 and D20Mit1, and between D14Got40 and D17Rat2 in the dorsal region phenotype. These results suggest that a major QTL in Chr 14, which is possibly correspondent to the hooded locus, mainly regulates the hooded phenotype with some modifier loci, two of which show epistatic interactions with the hooded locus.

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 study was conducted to determine the role of Ca2+ and K+ channels in Moringa oleifera flowers extract-induced myometrial contractility of buffalo uterus. Myometrial strips were prepared, mounted in an organ bath containing Ringer Locke solution maintained at 37oC and responses recorded using a kymograph. Moringa oleifera flowers extract (MOFE) produced quite conspicuous and concentration-dependent contractile effect on buffalo myometrium and the EC50 value was found to be 31.62 ìg/ml. Verapamil (10-12M) not only completely inhibited normal spontaneous rhythmic contractions of myometrial uterine strips but also inhibited MOFE-induced spontaneous rhythmic contractions. Ethylene glycol tetra acetic acid (EGTA; 0.1-0.2mM) reduced both the frequency and amplitude of spontaneous contractions and also produced around 28% reduction in the amplitude of MOFE-induced contractile effect. Similalrly, pinacidil (10-6M-10-5M), glibenclamide (10-5M) and 4- amino pyridine (4-AP; 1mM) pretreatments inhibited spontaneous contractions as well as the contractile effects of MOFE (250ìg/ml). Based on the results of present study, it may be inferred that both the extra- and intracellular Ca2+ are very vital for the oxytocic effect of MOFE. Functional presence of K+ ATP, K+ V and/or K+ Ca channels in buffalo myometrium and their involvement in mediating MOFEinduced contractility can not be ruled out. Moringa oleifera flowers possessed promising oxytocic activity and can be exploited in drug-development programme for evolving natural and effective oxytocic or abortifacient.

The calf was a congenital abnormal stillbirth of Sahiwal breed of zebu cattle, with multiple musculoskeletal defects. It was born to a heifer in its first calving. The calving was normal; however, calf born had multiple anomalies. The body of the calf was flashy just like a rubber balloon filled with water (case of hydropsy). The body was without hairs (hypotrichosis). Skeleton was noncalcified and ribs were cartilaginous. The body was identifiable in three regions: head, thoraxabdomen, and limbs. Morphologically limbs were developed but were quite short in length with well-developed hoof. There was one eye like structure just above the mouth (case of cyclopia). The tongue was developed and was protruded from mouth. There was one additional structure on the head, looked like outgrowth of muscles covered with thin skin, had openings of nostrils on the end. In autopsy abdominal body cavity was found filled with fluid. The visceral organ seemed normal. It was identified as female; however, ovaries and genital tract could not be traced and examined. It was the first calving of its dam with the complete gestation period of 287 days like a normal period in cattle. Pieces of tissue from lung and blood from the heart and vena cava were collected; however, cultures were found heavily contaminated with bacterial growth. The actual cause of the defects could not be established, might be defects of certain genes responsible for incomplete growth and development.

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.

A study was carried out in 2161 quarter milk samples of 550 cows in Durg district Chhattisgarh. Out of 550 animals, 385 (70%) animals were found to be positive for sub clinical mastitis (SCM) by Modified White Side Test (MWST), 432 (78.54%) by Modified California Mastitis Test (MCMT) and 462 (84%) by somatic cell count (SCC). The quarter wise prevalence of sub clinical mastitis was 47.99%, 55.25% and 60.90% by MWST, MCMT and SCC respectively. Prevalence of blind teats was 1.77%. prevalence was highest during second and third lactations and at 5 and 6 years of age. Infection rate was higher during early and late stages of lactation. HF and Jersey cross bred cows were more susceptible than indigenous cows. Microorganisms isolated were predominantly Staphylococci. ABST revealed sensitivity to cefotaxime whereas most of the isolates were resistant to ampicillin.