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Kerala Agricultural University, Thrissur

The history of agricultural education in Kerala can be traced back to the year 1896 when a scheme was evolved in the erstwhile Travancore State to train a few young men in scientific agriculture at the Demonstration Farm, Karamana, Thiruvananthapuram, presently, the Cropping Systems Research Centre under Kerala Agricultural University. Agriculture was introduced as an optional subject in the middle school classes in the State in 1922 when an Agricultural Middle School was started at Aluva, Ernakulam District. The popularity and usefulness of this school led to the starting of similar institutions at Kottarakkara and Konni in 1928 and 1931 respectively. Agriculture was later introduced as an optional subject for Intermediate Course in 1953. In 1955, the erstwhile Government of Travancore-Cochin started the Agricultural College and Research Institute at Vellayani, Thiruvananthapuram and the College of Veterinary and Animal Sciences at Mannuthy, Thrissur for imparting higher education in agricultural and veterinary sciences, respectively. These institutions were brought under the direct administrative control of the Department of Agriculture and the Department of Animal Husbandry, respectively. With the formation of Kerala State in 1956, these two colleges were affiliated to the University of Kerala. The post-graduate programmes leading to M.Sc. (Ag), M.V.Sc. and Ph.D. degrees were started in 1961, 1962 and 1965 respectively. On the recommendation of the Second National Education Commission (1964-66) headed by Dr. D.S. Kothari, the then Chairman of the University Grants Commission, one Agricultural University in each State was established. The State Agricultural Universities (SAUs) were established in India as an integral part of the National Agricultural Research System to give the much needed impetus to Agriculture Education and Research in the Country. As a result the Kerala Agricultural University (KAU) was established on 24th February 1971 by virtue of the Act 33 of 1971 and started functioning on 1st February 1972. The Kerala Agricultural University is the 15th in the series of the SAUs. In accordance with the provisions of KAU Act of 1971, the Agricultural College and Research Institute at Vellayani, and the College of Veterinary and Animal Sciences, Mannuthy, were brought under the Kerala Agricultural University. In addition, twenty one agricultural and animal husbandry research stations were also transferred to the KAU for taking up research and extension programmes on various crops, animals, birds, etc. During 2011, Kerala Agricultural University was trifurcated into Kerala Veterinary and Animal Sciences University (KVASU), Kerala University of Fisheries and Ocean Studies (KUFOS) and Kerala Agricultural University (KAU). Now the University has seven colleges (four Agriculture, one Agricultural Engineering, one Forestry, one Co-operation Banking & Management), six RARSs, seven KVKs, 15 Research Stations and 16 Research and Extension Units under the faculties of Agriculture, Agricultural Engineering and Forestry. In addition, one Academy on Climate Change Adaptation and one Institute of Agricultural Technology offering M.Sc. (Integrated) Climate Change Adaptation and Diploma in Agricultural Sciences respectively are also functioning in Kerala Agricultural University.

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1986 - 198911990 - 19981
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Author: Balagopalan, T P × Start date: 1980 ×
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    ThesisItemOpen Access
    Influence of glyceryl guaiacol ether on anaesthesia in goats
    (Department of Surgery, College of Veterinary and Animal Sciences, Mannuthy, 1986) Balagopalan, T P; KAU; Muraleedharan Nayar, K N
    The present study was undertaken with the object of finding out the influence of GGE and its combinations on anaesthesia in goats. Eighteen apparently healthy cross – bred male kids, aged 5 – 9 months, weighing 11 – 16 kg were used for the study in three groups of six animals each. GGE, five per cent solution alone at the rate of 100 mg/kg was administered intravenously in group A. Triflupromazine hydrochloride at the rate of 0.2 mg/kg and GGE solution at the rate of 100 mg/kg were administered in group B. Triflupromazine hydrochloride, GGE and five per cent Thiopentone sodium solutions were administered in group C. An average of 28.00 + 0.10 ml GGE solution was administered in group A, 0.12 + 0.003 ml Triflupromazine hydrochloride followed by 24.33 + 0.67 ml GGE solution in group B and 0.12 + 0.003 ml Triflupromazine hydrochloride, 28.83 + 0.54 ml GGE and 2.97 + 0.19 ml Thiopentone sodium solutions were administered in group C. There were no untoward symptoms at the time of administration of the drugs. The induction time was 3.42 + 0.20 min. in group A, 2.08 + 0.08 min. in group B and 2.40 + 0.24 min. in group C. The induction was smooth in all the groups. On induction pedal, corneal, cutaneous and palpebral reflexes disappeared in all the groups, while palpebral reflex alone persisted in group A. Dilation of pupil with complete relaxation of jaws, anus, penis and abdomen was noticed in all the animals as the anaesthetic effect deepened. Flaccidity of tail was pronounced in group C. All the animals were found to be weak and dull and did not take feed and water upto 12 hours in group A and upto 24 hours in group B and C. They were apparently normal by 24, 36 and 60 hours in group A, B and C respectively. Reduction in rectal temperature was noted in all the groups. Initial reduction followed by an increase in heart rate was seen in group B and C. In group A there was increase in heart rate from the beginning. Tachycardia was observed at the time of recovery in all the groups. The variations in respiration rate were within the normal limits. The duration of anaesthesia was 28.83 + 2.27 min., 44.83 + 1.74 min. and 52.60 + 3.57 min. in group A, B and C respectively. The period of recovery was 18.00 + 0.89 min., 17.33 + 1.05 min. and 34.40 + 1.69 min. in group A, B and C respectively. Recovery was smooth and uneventful. There was a significant fall in the blood pressure (systolic, diastolic and mean arterial pressure) in all the groups, but pulse pressure showed marginal variation. Variations in central venous pressure was not significant. The electrocardiogram revealed a depression of S – T segment in all the groups and depression of P wave in group B and C. Tachycardia was seen at recovery. There was reduction in total erythrocyte count while the leukocyte count showed an initial decrease followed by an increase at 24 hours. The lymphocyte count decreased and the neutrophil count increased. Variation in the eosinophil and monocyte count was not significant. A reduction in the haemoglobin content and packed cell volume was observed in all the groups. The erythrocyte sedimentation was observed in all the groups. The erythrocyte sedimentation rate showed an increase during anaesthesia. Significant increase in blood glucose was noticed in all the groups during anaesthesia and the serum protein values decreased. The serum sodium values showed marginal variations but the serum potassium values showed decrease upto 120 min. There was an increase in the serum chloride values followed by a decrease in all the groups. In all the three groups of animals, variation in serum glutamic pyruvic transaminase level was within normal limits. Gross lesions were not seen in any of the animals sacrificed on 4th or 10th day. But microscopic examination, early degenerative changes were noticed in the liver and kidney of all the animals sacrificed on the 4th day. Evidence of regeneration could be observed by the 10th day.
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    ThesisItemOpen Access
    Processed aortic allografts for oesophagoplasty in dogs
    (Department of Surgery, College of Veterinary and Animal Sciences, Mannuthy, 1998) Balagopalan, T P; KAU; Muraleedharan Nayar, K N
    The study was conducted with the objectives of a. Preparation, preservation and evaluation of chrome/ glutaraldehyde cross linked aortic tissue of dogs and to compare the relative acceptability and efficacy of them for cervical oesophagoplasty in dogs, and b. Evaluation of modified pharyngostomy feeding method and its effect on healing at cervical oesophagoplasty site in dogs. The experiment was conducted in thirty, apparently healthy, adult, nondescript dogs of either sex weighing 9-13 kg. The animals were randomly divided into three groups viz.,, group I, II and III. Group II and III were subdivided into two subgroups each, namely IIA, IIB and iilA, IIIB. Group I and the subgroups consisted of six animals each. Animals of group I were subjected to sham operation. Cervical oesophagoplasty using chrome processed aortic allograft and glutaraldehyde processed aortic allograft were performed in animals of group II and III respectively. Pharyngostomy tube feeding was instituted in three animals of group I and all animals of subgroups IIB and IIIB. Tissue samples of thoracic aorta harvested from dogs, processed and crosslinked with chromic sulfate and glutaraldehyde were used as graft materials. Chrome processed aorta showed better biomechanical qualities except for tensile strength than glutaraldehyde processed aorta. The grafts had fairly good handling qualities and shelf life. All the animals were premedicated with triflupromazine hydrochloride and anaesthetized using thiopentone sodium to effect. Wound, oval in shape measuring 3-4 cm long and l/3rd of the circumference of the oesophagus was created in all experimental animals. Oesophagoplasty was performed by fixing the graft material over the defect using 5-0 braided silk thread and continuous lock stitch sutures. Left side' pharyngostomy was performed in 15 dogs. Suitably designed siliconised catheter made up of modified polyvinyl chloride with an attached X-ray opaque line was used as pharyngostomy tube. The tube was kept in situ for a period of 15 days postoperatively for administration of fluid diet. The animals were kept under observation for varying periods of 15, 30 and 60 days postoperatively. The animals of subgroups IIB and IIIB became alert and active earlier than that of IIA and IIIA. At the cervical region, the operated site showed mild inflammatory reaction by 1-2 days postoperatively in all animals. The sutures were removed after normal healing by 7-8th day in all animals except one each in subgroup IIA and IIIB, where it was removed on the 10th day. Mild bleeding while performing pharyngostomy (one dog) and moderate pain and slight swelling around the pharyngostomy tube entrance site (3 dogs) were observed in subgroup IIB. One animal in subgroup IIIB showed severe inflammatory oedema around the tube entrance site. Tolerance of pharyngostomy tube was excellent in 13 dogs. The pharyngostomy wound healed completely by 14-15th day after removal of the tube in all the dogs. All the animals started feeding on liquid food by seventh day postoperatively in subgroups IIA and IIIA following hyperalimentation via intravenous route and by 15th day in subgroups IIB and IIIB following hyperalimentation via pharyngostomy tube. They maintained normal apetite and feeding habits thereafter during the period of observation. Mild swelling at the operated site while swallowing (3 dogs) and vomiting (one dog) were noticed among the animals of subgroup IIA and IIIA. Initial tube obstruction during first feeding (6 dogs), vomiting after first feeding (2 dogs) and mild diarrhoea (one dog) were observed among animals of subgroup IIB and IIIB.