GENERAL ARTICLEacids in the rumen, especially unsaturated fatty acids(UFAs) such as linoleic and linolenic (Czerkawski,1986). UFAs have toxic effects on methanogens andthe reduction in methanogenesis appears to be mostlya secondary effect on fermentation. Both in vivo andin vitro experiments have showed that addition of fatsand oils containing UFAs depressed fibre digestionas cellulolytic bacteria are sensitive to UFAs.Addition of alpha-tocopherol and beta-carotenealleviates the toxic effect of UFAs, and improvesfibre digestion.d. Halogenated Methane AnaloguesChlorinated methane analogues such aschloroform, carbon tetrachloride and methylenechloride inhibit methanogenesis in rumen.Halogenated alkanes also block the function ofcorrinoid enzymes (Vitamin B12dependent enzymes)in methanogenesis. Bromoethane sulfonic acid(BES) is a potent inhibitor of methanogenesis andgrowth of M. ruminantium. Among the halogenatedmethane analogues bromochloromethane (BCM)seems to be the most potent. (Trei et al., 1970;Sawyer et al., 1971; Chalupa, 1984).IIIVACCINESRecently scientists of CSIRO (Australia)developed vaccine against methanogens usingpseudumurein layer of its cell wall. This vaccinesuppress the growth of methanogens subsequentlyreduces methane production.CONCLUSIONRuminants are evidently major source ofmethane emission and so methane abundance wouldcontinue to grow in the atmosphere with rise inanimal number and production. Reduction ofmethane emission from ruminants can be achievedby several methods viz., supplementation of criticalnutrient through concentrate or green fodder, feedingurea molasses mineral block, defaunation variationof roughage: concentrate ratio, ammoniation ofcereal crop residues, feeding of halogenatedmethane, use of vaccines etc. If proper feedingstrategy and managemental practices are followed,methane production from ruminants can be reduced.It will improve the energy utilization /productionperformance of ruminants and protect theenvironment by reducing global warming.REFERRENCESChalupa, W. 1984. Manipulation of rumen fermentation.In: Recent Advances in Animal Nutrition (edited byharesign, W., Cole, D.), London, UK, Butterworths,pp 143-160.Czerkawski, J.W. 1986. Transfer of metabolic hydrogen inthe rumen. In: An introduction to rumen studies.Oxford, UK; Pergamon Press, pp. 173-188.Hino, T., Saitoh, H., Miwa, T., Kanda, M. and Kumazawa,S. 1993. Effect of aibelin, a peptide antibiotic, onpropionate production in the rumen of goats. J.Dairy Sci., 77: 3426-3431.Khan, M.Y., Murari Lal, Biswas, J.C., Haque, N. andGirdhar, N. 1996. Methane production from Indianlivestock. National Symposium. Prospects oflivestock and poultry development in 21st Century.CARI, Izatnagar, India, pp 41.Kreuzer, M., Kirchgessner, J. and Muller, H.L. 1986.Effect of defaunation on the loss of energy inweathers fed different quantities of cellulose andnormal or steam-flaked maize starch. Anim. FeedSci. Technol., 16: 233-241.Leng, R.A. 1991. Improving ruminant production andreducing methane emission from ruminants bystrategic supplementation. EPA, Washington, D.C.Preston, T.R. and Leng, R.A. 1987. Matching ruminantproduction system with available resources in thetropics and subtropics penumble books. ArmidaleAustralia.Sawyer, M.S., Hoover, W.H. and Sniffen, C.J. 1971.Effects of methane inhibitor on growth and energymetabolism in sheep. J. Dairy Sci., 34: 1191-1199.Trei, J.E., Singh, Y.K. and Scot, G.C. 1970. Effects ofmethane inhibition on rumen metabolism. J. Anim.Sci., 31: 256.Turnbull, G.W., Cripe, K. and Mishra, S. 2000. Effects ofmolasses urea supplementation of buffalo diet inGujarat state. India on work production, butterfat,animal weight and methane loss. In: Proceedings ofII International Methane Mitigation Conference,June 18-23; Novosibirsk, Russia.USEPA 1998. Small steps make a difference: Improvingyour cow-calf business and the emission of thesoutheastern USEPA 430-K-98-001, 12P.JIVA Vol. 10 Issue 1 <strong>April</strong> <strong>2012</strong>59
GENERAL ARTICLETERMINATION OF PREGNANCY IN BITCHESAbhilash.R.S, Anil kumar.K, Biju.S and Ajith.K.S,Livestock Research Station, Thiruvazhamkunnu, PalakkadJ. Ind. Vet. Assoc., Kerala. 10 (1)INTRODUCTIONTermination of pregnancy is one of the mostcommon requests from dog owners. The usualreasons include too young age, too old age,disproportionate size of mating partners or unwantedor accidental mating. Over the last 20 years manynew drugs have been used for termination ofpregnancy in canines. There are different treatmentprotocols such as oestrogen therapy, PGF2 and itsanalogues, dopamine agonists, combination ofprostaglandins and dopamine agonists, anti progestintherapy etc. Although most of these drugs havealready been used for years in other species, only feware widely marketed or approved for use in dogs. Theaim of the present article is to briefly review the stepsto be taken before proceeding with termination ofpregnancy, the drugs available for the termination ofpregnancy in bitches, their pharmacologicalproperties and availability.INITIAL EXAMINATIONA thorough history is valuable prior toattempt termination of pregnancy in bitch. Confirmwhether the animal has actually mated or not. Avaginal smear is the best diagnostic tool forevaluating mating and to find the stage of the cycle.The presence of sperm or sperm head confirmsmating whereas absence of sperm does not indicatethat a fertile breeding did not occur. Pregnancyshould be confirmed by ultrasound scanning aroundday 30 of the last breeding before starting thetreatment. The points to ponder in planning to abort abitch include its pregnancy confirmation and the60safety, reliability and the ease of administration ofthe drug used.The first stage of pregnancy begins atfertilization and ends a few days after implantation.During this time pregnancy cannot be confirmed andinduction of abortion is difficult because of therefractory nature of corpus luteum to exogenousmedications. Termination of pregnancy at this stagecan be attempted with medications like estrogens,prostaglandins and anti progestins. During thesecond stage, pregnancy can be confirmed andabortion can be induced if necessary. Abortion can beinduced with prostaglandins, antiprolactin agents(dopamine agonists such as bromocriptine orcabergoline), combination of prostaglandins anddopamine agonists or with inhibitors of progesteronesecretions (epostane) or antiprogestins (mifepristoneor aglepristone). Third stage is one that begins withthe calcification of fetal structures and abortion isalways associated with expulsion of foetus. In thisstage abortion might induce premature parturitionwith delivery of live pups. Hence the best time forinitiation of abortion protocols in bitches is betweendays 30 and 35 from the date of last breedingINDUCTION OF ABORTION PRIOR TOIMPLANTATIONFertilization of eggs and the initial 6-10 daysof embryonic development take place in theoviducts. Large doses of estrogens can prolongretention time of embryo within the oviduct thatleads to the degeneration and death of embryo. Themechanism of action of oestrogen is in two ways,firstly it tightens uterotubal junction and thus