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DOI :
Application of Ultrasonography to Investigate Postpartum Anestrus Buffaloes
1Department of Surgery and Obstetrics, Bangladesh Agricultural University
Department of Animal Science & Technology, School of Bioresource & Bioscience, Chung-Ang University, 3Department of Reproduction, Obstetrics and Herd Health, Ghent University, 4Department of Livestock Services.
Received: 4 May 2012, Accepted: 23 June 2012
Abstract
Anestrus is one of the most important production limiting disorders in dairy buffaloes and its underlying causes have been a current topic of studies. The objectives of this study were to explore the causes of anestrus in buffaloes with the application of ultrasonography. Two examinations were performed by transrectal ultrasonography at 12 days apart in buffalo cows that were not seen in oestrus at 60 or more days postpartum. As high as 54.5% buffaloes had silent ovulation and 45.5% suffered from the true anestrus with ovarian dysfunction. The duration of anestrus after calving was 60~90, 91~120, 121~180 and 181~365 days in 27%, 32%, 18% and 23% buffalo cows, respectively. Treatment with prostaglandin of cyclic buffalo cows with a corpus luteum (72.7%) resulted in higher estrous rate as compared with close observation of estrus (23.1%) by the farmer (p=0.021). Acyclic buffalo cows without any corpus luteum on ovaries were successfully treated with gonadotropin releasing hormone (70%), resulting in higher estrous detection rate than those treated with a vitamin-mineral mixture (20%) (p=0.035). In conclusion, poor heat detection due to silent ovulation is the most important cause of apparent anoestrus in buffaloes; however the percentage of the true anestrous is also quite high in postpartum buffaloes.
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INTRODUCTION

 Postpartum ovarian activity and subsequent conception may be affected by several factors such as breed, nutrition plan, milk yield, suckling, uterine involution, season of calving (Baruselli, 2001; Pipaon et al., 2002). The recent application of ultrasonographic techniques in the study of buffalo follicles is elucidating the patterns of follicular growth, development and regression has greatly improved our perceptive of the follicular dynamics in buffaloes (Henao et al., 2000; Presicce et al., 2003; Vassena et al., 2003). A good understanding of the processes involved in the growth and differentiation of vesicular follicles destined for ovulation is also essential in order to optimize buffalo reproduction. Ultrasonography for the assessment of ovarian structures is a reliable and accurate method for identifying and measuring follicles (Rahman et al., 2011), especially important since manual palpation per rectum in buffalo is not completely accurate. Gonadotropin releasing hormone (GnRH) administration in buffaloes induces ovulation in 60~86% of the treated animals (Aboul-Ela et al., 1985). This researcher’s also reported that, interval between GnRH administration and ovulation was 33±8.3 hours. Some other elegant study on this issue noted that, the presence of a dominant follicle at the time of GnRH administration is a pre-requisite for a successful induction of ovulation (Baruselli, 2001; De Rensis et al., 2005). Additionally, it is also reported that, administration of prostaglandins F2a (PGF2a) as early as Day 5 of the cycle induces CL regression (luteolysis), resulting in a dramatic decrease in within 2~6 days after the treatment (Brito et al., 2002). Single or double (with 11~14 days interval) PGF2a administration induces oestrus and ovulation in 60~70% of dairy buffaloes during the breeding season (Brito et al., 2002). Prostaglandins were only induces oestrus in buffalo, if a CL is present and therefore can be useful in case of silent ovulation. All of these methods for synchronization of estrus and ovulation are currently practiced in field condition, but still the rate of estrus and ovulation are remained questionable. Some researcher’s assume that, this condition might be subjected due to poor heat detection and silent heat. However, to date, the literature has not detailed a set of specific causes of anestrus in situ in indigenous buffalo of Bangladesh. Therefore, the current study was designed to explore the cyclical status of apparent anoestrus postpartum buffaloes and to test the effectiveness of oestrus induction in cyclic and non-cyclic buffaloes at 60 or more day postpartum with the application of ultrasonography.

MATERIALS AND METHODS

 The present study was conducted in the Field Fertility Clinic Laboratory (FFC), Department of Surgery and Obstetrics, Bangladesh Agricultural University, Mymensingh (BAU), Bangladesh.

Animal Selection and Management

 In total, 44 indigenous river-type buffaloes with post-partum anoestrus at 60 or more days were selected randomly from Trishal upazila and BAU dairy farms. The body condition score (BCS) of the buffalo cows varied from 2.5 to 4.0 (1.0=very thin to 5.0=very fat). Whereas, the parity of the buffaloes ranged from 1 to 6. The buffaloes were milked twice daily with their calves used for stimulating milk let down. Calves survived on residual milk after the hand milking. Weaning was not controlled in the buffaloes. The buffaloes were fed on rice straw, cut-and-carry grass and milling by-product as concentrate with limited grazing on roadside and community land. At lactation period, 0.5 to 1.5 kg concentrate (crashed rice and mustard oil cake) daily was given to each buffalo. Visual inspection of estrus sign and mating with fertile buffalo bull were practiced regularly.

Data Collection

 Data was collected from selected farm families and the dairy farm throughout the study period. Parity, duration of postpartum anestrus, milk yield and body condition score of the buffaloes with 60 or more days postpartum were recorded. The BCS of the buffalo cows (1.0=very thin to 5.0=very fat) was evaluated according to the procedures described elsewhere (Ahmed et al., 1999; Alapati et al., 2010).

e688c8ca4c14430a1f1384fe086df4d3.jpg.resized.jpgTable 1. Descriptive statistics of the study buffaloes

Reproductive Examination

 Buffalo cows with ≥60 days postpartum were examined by rectal palpation and transrectal ultrasonography (two examinations 12 days apart) to diagnose the underlying disorders. B-mode real-time ultrasonography (Tringa Linear VET® , Esaote Pie Medical, Genova, Italy) was used transrectally to examine the ovaries of buffaloes. After adequate restraining, the scanner was placed at a sensible distance from the cow on the side opposite to the operator΄s arm engaged in rectal palpation. All fecal materials from the rectum were evacuated prior to introduction of the transducer. The transducer face was lubricated with a suitable coupling medium (Ultrasonic Gel®  for Medical use-250 mg) and was usually covered by a lubricated plastic sleeve before insertion. The transducer was then progressed cranially along the rectal floor to overlie the reproductive tract. The ultrasound screen and the human eye were at similar level for accurate interpretation of ultrasound images. The ultrasound examination was carried out to identify the cyclic and non-cyclic buffaloes, based on the presence of corpus luteum (CL). To confirm the cyclic status, a second ultrasound examination was carried out 12 days later on those animals having no CL at the first monitoring (De Rensis et al., 2005). Based on the ovarian structures, the postpartum anestrous buffaloes were classified as follows:

 1. True anestrus (both ovaries found small, smooth, firm, with no corpus luteum).
 2. Silent heat (a corpus luteum was found on one of the ovaries while the uterus was considered to be symmetric).
 3. Uterine infection (detection of purulent material echogenic secretion in the body of uterus).
 4. Ovarian cyst (detection of a follicular structure or corpus luteum with ≥ 25 mm in diameter and persisting 10 or more days).

Experimental Design (Fig. 1)

87fb68c0bad611859754e9b2e448bdae.jpg.resized.jpgFig. 1. Schematic diagram showing the experimental designs.

Treatment of the Anoestrus Buffaloes

 Buffalo cows with a CL at either of the two examinations were considered as cyclic. They were injected intramuscularly with 25 mg PGF or advised to monitor heat carefully to breed on observed oestrus. Buffalo cows with inactive ovaries were treated with oral administration of a vitamin-mineral mixture or intramuscular injection of GnRH and bred at heat.

Statistical Analysis

 Descriptive statistics was done to determine the prevalence of anestrus in buffaloes. Differences in percentages of treatment outcome between two groups were analyzed by Fisher’s exact test. All statistical analyses were performed by using the Statistical Package for the Social Sciences (SPSS, 16.0 versions) software for windows.

RESULTS

Prevalence of Anestrus

 The prevalence of anestrus in postpartum buffaloes was 40% (44 out of 110). The prevalence was higher in summer (48.4%) than in winter (29.2%). In the anestrus buffaloes, 54.5% (24 out of 44) was cyclic evidenced by the presence of a corpus luteum (CL) and 45.5% (20 out of 42) buffalo cows were acyclic, which was manifested by small ovaries without a corpus luteum (Table 2).

b1b6d8e58610eb88c9fd919f4874d8e9.jpg.resized.jpgTable 2. Characteristics of apparently anestrous water buffaloes

 The duration of anestrus after calving was 60~90, 91~120, 121~180 and 181~365 days in 27%, 32%, 18% and 23% buffaloes respectively (Table 3).

d8a328139a09e3c31799cb09b2393b70.jpg.resized.jpgTable 3. Interval in months from last calving to diagnosis of anestrus in buffaloes

Treatment of Anestrus

 Treatment of cyclic buffalo cows having a CL with prostaglandin (72.7%) resulted in higher rate of detection than that with close observation (23.1%) for estrus by the farmer (p=<0.050; Table 4). Acyclic buffalo cows bearing no corpus luteum on ovaries were successfully treated with GnRH (70%) resulting in higher rate of estrous detection than those treated with a vitamin-mineral mixture (20%) (p<0.05; Table 4).

2e62e928c88edaa53c7d7a5eff4c292c.jpg.resized.jpgTable 4. Reproductive performance of anestrus buffalo cows after PGF treatment

 The buffaloes having post partum anestrus ≥60 days were allocated primarily into two groups buffaloes with CL on ovaries (non-detected estrus) and without CL (true anestrus). Later on, the buffalo cows with CL on ovary were treated by either PGF2a or assigned to close observation of estrus by farmer to detect the buffaloes at heat. Whereas, buffaloes without detectable CL on ovary (true anestrus), were treated by GnRH or vitamin-mineral premix.

DISCUSSION

Prevalence of Anestrus

 Anestrus in buffaloes is generally caused by ovarian dysfunction or silent ovulation. Previous clinical surveys reported cases of anestrus showed that about 60% of cases were true anestrus and 33% of cases were silent ovulation (Sah and Nakao, 2010). In the present study, among the 110 buffalo cows examined 45% had inactive ovaries (true anestrus), while 55% had silent ovulation or missing heat. Ovarian cysts were diagnosed in only 5.2% of the cows (Reddy et al., 1986), which was also not well comparable with this study. In this survey, 32% of the anestrus cows were at 90~120 days postpartum and 42% were at more than 120 days postpartum. In the survey, 61.5% of the anestrus cows were already at 10~15 months after calving and 31.9% were at more than 16 months postpartum (Sah and Nakao, 2010). This is due partly to the limited availability of veterinary service and to the producer’s attitude towards cows; as long as the cows are producing a certain amount of milk, they do not pay much attention to re-breeding the cows. Season of calving influences the reproductive performance. Numerous worker reported that buffaloes calving in the rainy and monsoon seasons had shorter anestrous periods than those calved in other seasons (Reddy et al., 1986; Sule et al., 2001). Nevertheless, longer anestrous periods were reported for out of season (156±34 and 91±12 days) than normal breeding season calvers (57±6 and 56±5 days) (Qureshi et al., 1998). The prevalence of anestrus in postpartum buffaloes was higher in summer than in winter in the present study. Majority of the buffaloes during summer had silent ovlution (Chaudhry, 1988), characterized by less intense overt signs of oestrus with shorter duration (Jainudeen and Hafez, 2000). A research in the Pakistani river buffalo showed that 51.5% of estrus was the silent heat (Qureshi and Ahmad, 2008). Whereas, someother found problems of difficult calving was highest during autumn, followed by rainy and summer months (Kaushik and Mathur, 2005). It is well know that in buffalo species, the ability of detect estrus declines during the warmest hours of the day and in animals with heat stress (Vale et al., 1988).

Treatment of Anestrus

 Treatment of silent ovulation with prostaglandin in buffalo cows with a corpus luteum (CL) resulted in higher oestrus rate within one month after treatment as compared with treatment with close observation for heat by the farmer. Buffaloes with a CL responded well to PGF2a, with high estrus induction and pregnancy rates, as already reported by a number of studies (Chauhan et al., 1982; Dhaliwal et al., 1988). The efficacy of the prostaglandin treatment in buffaloes to regress a functional CL was reported to be dependent on plasma progesterone concentration, the CL size and the ovarian follicular status before prostaglandin administration (Brito et al., 2002). Nevertheless, in buffaloes the occurrence of the inadequate luteal phase due to short time CLs or characterized by insufficient progesterone production has been reported, which in turn may explain the unsatisfactory response to prostaglandin administration for control of reproductive function (Zicarelli et al., 1988). However, improvements are recorded when prostaglandin is followed by GnRH administration (Neglia et al., 2011). In addition with the possibility of the use of hormonal control of the estrous cycle, seasonal pattern can be overcome and they can be bred through the synchronization of the estrous cycle in year around (Vale and Ribeiro, 2005).

 Buffalo cows with inactive ovaries were successfully treated with GnRH resulting in higher oestrus rate within one month after treatment than those treated with vitamin-mineral mixture. The interval after GnRH to ovulation was 36 h in buffaloes (Baruselli et al., 2003). During the last few years, several studies have been attempted to treat the prolonged postpartum anestrum in buffaloes by using hormonal treatments such as GnRH, prostaglandin F2α (Metwelly, 2001; 2006). It has also been reported that GnRH is effective in inducing ovulation in buffaloes (Pattabiraman et al., 1986; Thakur et al., 1993). The results of this study correspond to these earlier reports. The efficacy of PGF and GnRH in anestrous buffaloes shown by the present study and the earlier reports mentioned above suggests that routine reproductive examination of buffaloes that are not observed to be in estrus and adequate treatment may improve reproductive efficiency in buffaloes. The commonly practiced method of treatment of anestrus in buffaloes in this region has been use of a vitamin/mineral mixture, which was shown to be less effective than administration of hormones.

 In conclusion, the predominant causes of anestrus in dairy buffaloes studied were silent ovulation; however true anestrus was also common and the duration of anestrus after calving and breeding was extremely long. Routine reproductive examination and adequate hormone treatment may improve the reproductive performance of these buffaloes.

Reference
1.Aboul-Ela MB, El-Keraby FE, Khattab R (1985): Effect of GnRH treatment on postpartum resumption of oestrus and ovulation in buffaloes. Buffalo J 1:61-69.
2.Ahmed WM, Abdoon AS, Shalaby SI, Kandil OM (1999): Effect of reproductive status and body condition score on ovarian follicles and oocytes quality in buffalo-cows. Buffalo J 15:333-343.
3.Alapati A, Kapa SR, Jeepalyam S, Rangappa SM, Yemireddy KR (2010): Development of the body condition score system in Murrah buffaloes: validation through ultrasonic assessment of body fat reserves. J Vet Sci 11:1-8.
4.Baruselli PS (2001): Control of follicular development applied to reproduction biotechnologies in buffalo. In: Proceedings of the I Congresso Nazionale sull' Allevamento del Bufalo, Italy, Book of the Congress 128-146.
5.Baruselli PS, Madureira EH, Banarka VH, Barnarbe RC, Cassimiro R (2003): Evaluation of synchronization of ovulation for fixed time insemination. Brazilian J Vet Res Anim Sci 40:431-442.
6.Brito LF, Satrapa R, Marson EP, Kastelic JP (2002): Efficacy of PGF (2 alpha) to synchronize estrus in water buffalo cows (Bubalus bubalis) is dependent upon plasma progesterone concentration, corpus luteum size and ovarian follicular status before treatment. Anim Reprod Sci 73:23-35.
7.Chaudhry RA (1988): Recent advances in female reproduction. In: Proceedings of Second World Buffalo Congress, Delhi, India II, 225-228.
8.Chauhan FS, Sharma RD, Singh GB (1982): Responses of different doses of prostaglandin F2 alpha on estrus induction, fertility and progesterone levels in suboestrus buffaloes. Theriogenology 17:247-253.
9.De Rensis F, Ronci G, Guarneri P, Nguyen BX, Presicce GA, Huszenicza G, Scaramuzzi RJ (2005): Conception rate after fixed time insemination following ovsynch protocol with and without progesterone supplementation in cyclic and noncyclic Mediterranean Italian buffaloes (Bubalus bubalis). Theriogenology 63:1824-1831.
10.Dhaliwal GS, Sharma RD, Singh G (1988): Efficacy of prostaglandin F2 alpha administration for inducing oestrus in buffalo. Theriogenology 29:1401-1406.
11.Henao G, Oliver-Angel M, Maldoado-Estrada JG (2000): Follicular dynamics during postpartum anestrous and the first estrous cycle in suckled or nonsuckled Brahman (Bos indicus) cows. Anim Reprod Sci 63:127-136.
12.Jainudeen MR, Hafez ESE (2000): Reproductive cycles in cattle and buffaloes, In: Hafez ESE, Hafez B (eds), Reproduction in Farm Animals, 7th edition, Lea and Febiger, Baltimore, Maryland, USA, 297-314.
13.Kaushik SK, Mathur AC (2005): Time of parturition and incidences of calving abnormalities in Murrah buffaloes. Indian J Anim Sci 75:277-278.
14.Metwelly KK (2001): Postpartum anestrus in buffalo cows: causes and treatment, Proceedings of the Sixth Scientific Congress Egyptian Society for Cattle Diseases, Assiut, Egypt. Assuit: Assuit University, 259-267.
15.Metwelly KK (2006): Treatment of ovarian inactivity in postpartum buffalo-cows with special reference to its economic evaluation. Assiut Vet Med J 52:214-225.
16.Neglia G, Vecchio D, Russo M, Di Palo R, Pacelli C, Comin A, Gasparrini B, Campanile G (2011): Efficacy of PGF on pre-ovulatory follicle and corpus luteum blood flow. Reprod Domest Anim doi: 10.1111/j.1439-0531.2011.01794.x.
17.Pattabiraman SR, Veerapandian C, Quayam SA (1986): Effect of receptal treatment in anoestrus and early post-partum cows and buffaloes. Ind Vet J 63:409-413.
18.Pipaon EC, Alonso JC, Hincapie JJ, García L, Faure O, Fernández O (2002): Seasonal influence on uterine involution and postpartum ovarian activity in river buffaloes (Bubalus bubalis), Proceedings of the 1st Buffalo Symposium of Americas, Brazil, 456-459.
19.Presicce GA, Parmeggiani A, Senatore EM, Stecco R, Barile VL, De Mauro GJ, De Santis G, Terzano GM (2003): Hormonal dynamics and follicular turnover in prepuberal Mediterranean Italian buffaloes. Theriogenology 60:485-493.
20.Qureshi MS, Ahmad N (2008): Interaction of calf suckling, use of xytocin and milk yield with reproductive performance of dairy buffaloes. Anim Reprod Sci 106:380-392.
21.Qureshi MS, Samad HA, Nazir Ahmad N, Habib G, Anjun AD, Siddiqui MM (1998): Reproductive performance of dairy buffaloes under peri-urban commercial farming in VWFP, Pakistan. Pakistan Vet J 18:197-201.
22.Rahman MS, Shohag AS, Kamal MM, Bari FY, Shamsuddin M (2011). Preovulatory follicular and subsequent luteal size influence pregnancy success in water buffaloes. J Reprod Dev 58:219-222.
23.Reddy AO, Tripathi NN, Raina VS (1986): Factors affecting postpartum reproductive performance in Murrah buffaloes. Indian J Anim Sci 56:1224-1228.
24.Sah SK, Nakao T (2010): A clinical study of anestrus buffaloes in Southern Nepal. J Reprod Develop 56:208-211.
25.Sule SR, Taparia AL, Jain LS, Tailor SP (2001): Reproductive status of Surti buffaloes maintained under sub-humid conditions of Rajasthan. Indian Vet J 78:1049-1051.
26.Thakur MS, Gour AK, Vatta VK, Shriwastava S (1993): Efficacy of receptal in induction of estrus in buffaloes by different doses and route of administration. Ind J Anim Reprod 14:16-17.
27.Vale GW, Ohashi OM, Sousa JS, Rebiero HF (1988): Clinical reproductive problems of buffaloes in Latin America, Proceedings of the Second World Buffalo Congress, New Delhi, India, 206-217.
28.Vale WG, Ribeiro HFL (2005): Características reprodutivas dos bubalinos: puberdade, ciclo estral, involução uterina e atividade ovariana no pós-parto. Rev Bras Reprod Anim, Belo Horizonte. Rev Bras Reprod Anim 29:63-73.
29.Vassena R, Adams GP, Mapletoft RJ, Pierson RA, Singh J (2003): Ultrasound image characteristics of ovarian follicles in relation to oocyte competence and follicular status in cattle. Anim Reprod Sci 76, 25-41.
30.Zicarelli L, Infascelli F, Esposito L, Consalvo F, De Franciscis G (1988): Influence of climate on spontaneous and alfaprostol induced heats in Mediterranean buffalo cows bred in Italy, Proceedings of II World Buffalo Congress held in India during 12-16 December 1988. pp. 49-56.

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