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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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1989 - 198912000 - 20071
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Subject: Veterinary Pharmacology and Toxicology × Author: KAU × Author: Usha, P T A × End date: 2022 ×
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    ThesisItemOpen Access
    Influence of buprenorphine , pentazocine and xylazine analgesia on ketamine anaesthesia in dogs
    (Department of Pharmacology, College of Veterinary and Animal Sciences, Mannuthy, 1989) Usha, P T A; KAU; Rajagopalan, N K
    The experiments were conducted in three different parts. In the first part of the experiment the ED50 of the three drugs namely buprenorphine, pentazocine and xylazine was determined using the analgesiometer (tail flick method) in rats and tail clip method in mice. The ED50 of buprenorphine in rats and mice was 0.25 + 0.084 mg/kg and 0.9827 + 0.0751 mg/kg intraperitoneally. The ED50 of pentazocine in rats was 32.60 + 0.071 mg/kg and in mice 48.50 + 0.323 mg/kg. The ED50 of xylazine for analgesia in rats and mice was 1.424 +0.229 mg/kg and 7.523 + 0.47 mg/kg respectively. In the second part of the experiment the influence of buprenorphine, pentazocine and xylazine analgesia on ketamine anaesthesia in dogs were studied. Twenty – four animals divided into four groups (A(K), B(X-K), C(B-K) and D(P-K) were administered with ketamine (20 mg/kg), xylazine (2 mg/kg) plus ketamine (15 mg/kg), buprencrphine (0.03 mg/kg) plus ketamine (15 mg/kg) and pentazocine (2 mg/kg) plus ketamine (15 mg/kg) respectively. The sternal recumbency time, clinical signs, duration of anaesthesia, regaining of sternal recumbency time, mean standing time, total recovery time and haemogram were studied. The sternal recumbency time was minimum in xylazine administered group. Untoward reactions like salivation and rigidity of the muscles were observed in groups A(K) and D(P-K). There was significant reduction in rectal temperature in all the groups. The pulse rate was elevated in group A(K) and depressed in group B(X-K), while a transient increase followed by decrease showed in group C(B-K) and D(P-K) . Respiratory depression was observed in groups C(B-K) and D(P-K). Average duration of anaesthesia was maximum in group B(X-K) while all other groups showed almost similar durations of anaesthesia. The time for regaining of sternal recumbency was also maximum in group B(X-K), then the groups A(K), C(B-K) and D(P-K) respectively. Mean standing time was maximum in group B(X-K). The rest of the groups followed the same pattern as above. The total recovery time was maximum in group C(B-K), then group B(X-K), A(K) and D(P-K) respectively. The study of haemogram showed that, the haemoglobin, packed cell volume and erythrocyte counts decreased at 30 min. after drug administration in groups A(K) and B(X-K) while there was no significant variation in group C(B-K) and D(P-K). The group D(P-K) showed a significant reduction in leucocyte count, while there were no variations in other groups observed. In the third part of the experiment the reversal of anaesthesia using the 2 blocker yohimbine was studied. Twenty-four animals divided into four groups (E,F, G and H) were administered with the same drugs as in the second part of the experiment. Along with that yohimbine (0.25 mg/kg in group E, G and H and 2 mg/kg in group F) was administered 15 min. later. The groups E, F, G and H were designated as K-Y, X-K-Y, B-K-Y and P-K-Y respectively. Uptoward effects exhibited after yohimbine administration were salivation, panting and hyperaesthesia during recovery. Rectal temperature, pulse and respiration were increased in all the groups. The duration of anaesthesia, regaining of sternal recumbency time, mean standing time and total recovery time were significantly reduced in group F(X-K-Y), while there was no variation in the above parameters in group E(K-Y). Only the total recovery time significantly reduced in group G(B-K-Y) and prolongation of standing time and total recovery time was observed in group H(P-K-Y). The haematological changes noticed in the second part of the experiment were completely reversed by yohimbine.
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    ThesisItemOpen Access
    Identification of toxic fractions of Mimosa invisa (Anathottavadi) and its toxicity in rabbits
    (Department of Pharmacology and Toxicology, College of Veterinary and Animal Sciences, Mannuthy, 2007) Usha, P T A; KAU; Gopakumar, N
    The present study was undertaken to identify the toxic fraction of Mimosa invisa in rabbits and to assess to toxicity of Mimosa invisa fresh juice, cold alcoholic extract and various fractions of alcoholic extract utilizing rabbit as a model along with treatment study. The experiment was conducted in two phases. The first part of the study involved assessment of toxicity of fresh juice of Mimosa invisa (group II) and cold alcoholic extract (group Ill). Group I served as control. The preliminary tests were conducted to derive the toxic dose of fresh juice and alcoholic extract of Mimosa invisa. The toxic doses were 25 g/kg and 1 g/kg body weight for Mimosa invisa fresh juice and alcoholic extract respectively. The clinical symptoms, biochemical parameters and haemogram were observed to assess the toxicity. The serum ALT, AST and GGT levels showed significant increase in both the groups. The serum creatine kinase levels exhibited an increase followed by a decrease. There was a significant increase in serum creatinine and urea levels. There were no changes in serum total protein, albumin, globulin and albumin-globulin ratio. Significant decrease in VPRC, haemoglobin and RBC count could be noticed. The erythrocyte indices did not show any variations. The leucocytosis was observed in group II and III when compared to control (group I). Lymphocytosis with neutropenia were also observed in both the groups. The second phase of the study involved identification of toxic dose of each fraction of Mimosa invisa: The preliminary studies revealed that chloroform fraction (Fraction I) and water insoluble residue (fraction IV) were not toxic to rabbits while the fraction II (n-butanol fraction) and fraction III (aqueous fraction) were toxic to rabbits. Hence the two toxic fractions were pooled and used for further studies. It was found that 0.4 g/kg of pooled toxic fraction was toxic in rabbits. The toxicity was assessed by the evaluation of clinical symptoms, biochemical parameters and haemogram. The group V (pooled toxic fraction) showed inappetence, dullness, lethargy and reluctant to move. A significant increase in serum ALT, AST and GGT levels were observed. The serum ALP levels showed an increase followed by a decrease. The serum creatine kinase also showed similar increase followed by decrease. The creatinine and urea levels exhibited a continuous increase in group V. There were no changes in total protein, albumin, globulin and albumin-globulin ratio. The VPRC, RBC and haemoglobin showed significant decrease but there were no changes in erythrocyte indices. A significant leucocytosis was observed in group V. The differential leucocyte count showed lymphocytosis with neutropenia. The group VI (Half the toxic dose of pooled toxic fraction) failed to produce toxicity as evidenced by biochemical parameters and haemogram. The group VII (Double the toxic dose of pooled toxic fraction), all the animals died within 12-24 hours of administration of the dose. The group VIII animals were treated with a decoction prepared from equal quantities of Boerhvia diffusa, Hygrophila auriculata and Tribulus terrestris along with pooled toxic fraction of Mimosa invisa. The prominent symptom of inappetence was only for a short period of time (1-2 day). Then the animals started taking normal feed and water. The serum AL T, AST and GGT levels were significantly increased during the first five days, then the values returned to normal level. The serum creatine kinase and ALP levels did not show significant changes. The serum creatinine and urea levels showed significant increase followed by decrease. All the parameters showed significant improvement when compared with group V (pooled toxic fraction alone). There were no changes in serum protein, 'albumin, globulin and albumin-globulin ratio. The screening of alcoholic extract and various fractions revealed that the alcoholic extract n-butanol fraction and aqueous fraction contained steroids phenolic compounds, tannins, flavonoids, glycosides, diterpenes triterpenes and saponins. The chloroform fraction was positive for flavonoids only, whereas water insoluble fraction contained flavonoids and traces of tannins, triterpenes and saponins. From the results of the present study, it is concluded that the phytotoxin present in M invisa is nephrotoxic and hepatotoxic. The treatment schedule tried using a decoction of Boerhavia diffusa, Tribulus terrestris and Hygrophila auriculata could protect kidney and liver from the phytotoxin present in M invisa. Further study is needed to isolate the phytotoxin present in M invisa so that a specific antidote can be developed.