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Reproduction in Domestic Animals

Reproduction in Domestic Animals

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Reproductive Physiology, Pathology and AI <strong>in</strong> Cat 147this method (Chatdarong et al. 2007). Addition ofEquex STM (Nova Chemical Sales, Scituate Inc., MA,USA) paste to a Tris–egg yolk extender reduces acrosomedamage after freez<strong>in</strong>g-thaw<strong>in</strong>g, but may have atoxic effect dur<strong>in</strong>g <strong>in</strong>cubation, lead<strong>in</strong>g to a fasterdecrease <strong>in</strong> sperm viability (Axnér et al. 2004). Wash<strong>in</strong>gfrozen-thawed spermatozoa by centrifugation to removethe freez<strong>in</strong>g extender <strong>in</strong>clud<strong>in</strong>g the Equex STM pastehad, however, no beneficial effect on sperm longevity <strong>in</strong>a prelim<strong>in</strong>ary study (Axne´r et al. 2006). Addition ofantioxidants to the freez<strong>in</strong>g buffer has been shown toimprove post-thaw cat epididymal sperm quality(Luvoni et al. 2002; Thuwanut et al., 2008).Ovulation <strong>in</strong>duction and tim<strong>in</strong>g of <strong>in</strong>sem<strong>in</strong>ationIn the absence of the mat<strong>in</strong>g stimuli, ovulation must beartificially <strong>in</strong>duced before AI can be carried out. Thelarge variation <strong>in</strong> the female oestrous cycle complicatesdeterm<strong>in</strong>ation of the optimal time for ovulation <strong>in</strong>duction.Ultrasound evaluation may be a reliable method tofollow follicular maturation (Malanda<strong>in</strong> et al. 2002).The occurrence of spontaneous ovulation may contributeto difficulties <strong>in</strong> tim<strong>in</strong>g the AI (Lawler et al. 1993;Chatdarong et al. 2007). In order to control the oestrouscycle, studies on different hormonal therapies have beenperformed (Pelican et al. 2006). Pharmacological <strong>in</strong>ductionof oestrus and ovulation cause, however, abnormalhormonal profiles that may <strong>in</strong>terfere with fertility(Pelican et al. 2006). Ovulation <strong>in</strong>duction is usuallycarried out with one or two <strong>in</strong>jections of hCG <strong>in</strong>midoestrus (Pelican et al. 2006; Tsutsui 2006; Chatdaronget al. 2007). For <strong>in</strong>duction of oestrus, a comb<strong>in</strong>ationof eCG with an <strong>in</strong>jection of hCG 80–84 h later isoften used (Pelican et al. 2006). Both hCG and eCGstimulate the production of antibodies, hence, frequentadm<strong>in</strong>istration can lead to decreased treatment success(Pelican et al. 2006). The optimal protocol for ovulation<strong>in</strong>duction and tim<strong>in</strong>g of ovulation <strong>in</strong>duction rema<strong>in</strong>s tobe elucidated.Spermatozoa should be <strong>in</strong>sem<strong>in</strong>ated with<strong>in</strong> 49 hafter ovulation <strong>in</strong>duction as no fertilizations have beenobserved to occur after this time (Sojka et al. 1970;Howard et al. 1992). Fel<strong>in</strong>e spermatozoa probably donot require a long time for capacitation. Niwa et al.(1985) reported that 100% of homologous oocyteswere penetrated by epididymal spermatozoa with<strong>in</strong>30 m<strong>in</strong> after <strong>in</strong>sem<strong>in</strong>ation, while ejaculated cat spermatozoaseem to need 2.5–3 h for <strong>in</strong> vitro capacitation(Long et al. 1996). Consider<strong>in</strong>g the reduced longevityof frozen-thawed spermatozoa, they should probablybe <strong>in</strong>sem<strong>in</strong>ated close to ovulation. The optimal timefor AI <strong>in</strong> relation to ovulation has, however, not beenfully elucidated although some studies report AI atdifferent times with some conflict<strong>in</strong>g results concern<strong>in</strong>gthe effect of pre-ovulatory anaesthesia on ovulation(Howard et al. 1992; Tsutsui 2006; Chatdarong et al.2007).Techniques of semen depositionPregnancies have been achieved with <strong>in</strong>travag<strong>in</strong>al as wellas with surgical or laparoscopic <strong>in</strong>trauter<strong>in</strong>e or <strong>in</strong>tratubalsemen deposition (Sojka et al. 1970; Platz et al.1978; Howard et al. 1992; Tsutsui 2006; Tsutsui et al.2001). In most species as well as <strong>in</strong> the cat, <strong>in</strong>trauter<strong>in</strong>esemen deposition yields better pregnancy results thanvag<strong>in</strong>al deposition although the cat spermatozoa aredeposited <strong>in</strong> the vag<strong>in</strong>a dur<strong>in</strong>g natural coitus (L<strong>in</strong>de-Forsberg et al. 1999; Tanaka et al. 2000; Thomassenet al. 2006; Tsutsui 2006; Chatdarong et al. 2007).Surgical <strong>in</strong>sem<strong>in</strong>ation is an <strong>in</strong>vasive procedure that isnot allowed <strong>in</strong> all countries. Therefore, studies ontranscervical AI have been performed. Transcervicalcatheterization <strong>in</strong> the cat is, however, associated withdifficulties because of the vag<strong>in</strong>al anatomy. Abdom<strong>in</strong>alfixation of the cervix as carried out with the Norwegiantranscervical catheter for the bitch is not possible <strong>in</strong> thequeen because of the position of the cervix and thenarrow cranial vag<strong>in</strong>a makes endoscopy-guided transcervicalpassage impossible (L<strong>in</strong>de-Forsberg et al. 1999;Chatdarong et al. 2002; Zambelli et al. 2004; Thomassenet al. 2006). Zambelli and Castagnetti (2001)performed rectally guided transcervical catheterizationus<strong>in</strong>g a rounded tip needle <strong>in</strong>serted at the cut end of a 3-Fr tomcat catheter.Birth of live kittens has resulted after transcervical<strong>in</strong>trauter<strong>in</strong>e deposition of frozen-thawed semen with thehelp of a catheter modified from a transcervical catheterfirst described by Swanson and Godke (1994) (Chatdaronget al. 2005, 2007). The result with birth of livekittens is promis<strong>in</strong>g for the use of non-surgical AI <strong>in</strong>small felids, although the protocol still needs to beref<strong>in</strong>ed to improve pregnancy results and to allow theuse of a lower sperm number (Chatdarong et al. 2007).In conclusion, although more studies on evaluation offollicular maturation, protocols for artificial ovulation<strong>in</strong>duction, semen conservation and techniques of AI areneeded before an optimal protocol for rout<strong>in</strong>e AI <strong>in</strong> thecat can be developed, some promis<strong>in</strong>g progress has beenachieved <strong>in</strong> the development of semen conservation andAI <strong>in</strong> the cat.ReferencesAxne´r E, L<strong>in</strong>de Forsberg C, 2007: Sperm morphology <strong>in</strong> thedomestic cat, and its relation with fertility: a retrospectivestudy. Reprod Domest Anim 42, 282–291.Axne´r E, Stro¨m B, L<strong>in</strong>de-Forsberg C, Gustavsson I, L<strong>in</strong>dbladK, Wallgren M, 1996: Reproductive disorders <strong>in</strong> 10 domesticmale cats. J Small Anim Pract 37, 394–401.Axne´r E, Stro¨m Holst B, L<strong>in</strong>de Forsberg C, 1998: Morphologyof spermatozoa <strong>in</strong> the cauda epididymidis beforeand after electroejaculation and a comparison with ejaculatedspermatozoa <strong>in</strong> the domestic cat. Theriogenology50, 973–979.Axne´r E, Hermansson U, L<strong>in</strong>de-Forsberg C, 2004: The effectof Equex STM paste and sperm morphology on post-thawsurvival of cat epididymal spermatozoa. Anim Reprod Sci84, 179–191.Axne´r E, Kronsell A, L<strong>in</strong>de-Forsberg C, 2006: Effect of postthawcentrifugation on viability of epididymal cat spermatozoa.<strong>in</strong>: Luvoni GC, Thuro´czy J (eds), Proc. 5th BiannualEVSSAR Conf. Budapest, April, P06.Axne´r E,A˚ gren E, Ba˚ verud V, Stro¨m Holst B. Infertility <strong>in</strong> thecycl<strong>in</strong>g queen: seven cases. Journal of fel<strong>in</strong>e medic<strong>in</strong>e andsurgery, 2008: DOI: 10.1016/j.jfms.2008.04.005.Ó 2008 The Author. Journal compilation Ó 2008 Blackwell Verlag

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