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Developmental comparisons of boars and barrows: II. Body composition and bone development.

Differences in total carcass bone, muscle and fat, and linear measurements of the tibia and radius were evaluated in barrows at 105 kg and boars at 105, 118, 132 and 145 kg live body weight. The carcasses of five replicates were physically separated into skin, bone and soft tissues, and the linear measurements of the tibia and radius were obtained on seven replicates. At live weight of 105 kg, boars did not differ significantly in fat-free muscle, but they had 33.2% less fat, 11% greater bone weight and 14% greater skin weight than barrows. At 145 kg, boars had total carcass fat weight comparable with 105-kg barrows. Fat-free muscle, bone and skin weight of boars increased at linear rates of .41, .083 and .104 kg/kg of body weight increase from 105 to 145 kg, respectively. At 105 kg, density and length of the tibia and radius did not differ between boars and barrows. The tibia of boars were heavier than those of barrows at 105 kg, resulting in a greater ratio of tibia weight to length (indirect measure of bone thickness). As boars increased in live weight from 105 to 145 kg, total weight and length of the tibia and radius increased linearly. The ratio of weight to length of the tibia and radius increased during this 40-kg weight gain, indicating that weight of both bones increased at a greater rate than length. These results indicate that boars and barrows have the same weight of total carcass fat when boars are 40 kg heavier than the barrows. The greater bone weight of boar carcasses compared with barrows is due to greater bone thickness.

Adipose Tissue↗

Body growth and testicular characteristics of boars fed a synthetic progestogen, altrenogest.

A synthetic progestogen (altrenogest) was fed to 24 Yorkshire X Duroc boars to determine effects on body growth, serum testosterone, and testicular characteristics. Boars from six litters (blocks) were allotted randomly to one of four treatment groups at 12 wk of age. Treatment groups were: controls, altrenogest fed for 3 wk, altrenogest fed for 6 wk and altrenogest fed for 9 wk. Treatment began at 15 wk of age at a daily dose of 20 mg X boar-1. Although there were no differences among treatment groups for gain and feed intake, boars fed altrenogest for 6 and 9 wk tended to consume more feed and were less (P less than .05) efficient than boars fed altrenogest for 3 wk or controls. Boars fed altrenogest for 3, 6 and 9 wk maintained lower (P less than .05) peripheral serum testosterone concentrations than controls from 15 to 24 wk of age. However, serum testosterone increased after altrenogest withdrawal in the 3- and 6-wk treatment groups but did not reach control concentrations by 24 wk. Boars fed altrenogest for 9 wk maintained serum testosterone below 1 ng/ml during the treatment period. Despite lower concentrations of serum testosterone in altrenogest-treated boars, backfat thickness was similar to controls, perhaps suggesting a slight anabolic effect of altrenogest on nutrient partitioning. Testicular weights and volumes at 24 wk decreased (P less than .001) linearly with increased duration of altrenogest feeding. Serum testosterone and estradiol in testicular venous effluent at castration were lower (P less than .01) in altrenogest-treated boars than in controls. These data demonstrate that feeding altrenogest inhibits both testicular growth and steroidogenesis of boars without altering body growth or backfat thickness.

Animals↗

The effect of duration of boar exposure on the frequency of gilts reaching first estrus.

One-hundred crossbred gilts were used in an experiment that was designed to examine the effects of duration of boar exposure on the proportion of gilts reaching first estrus. Two replicates (summer and fall) of 50 gilts each were randomly assigned, within litter, to one of the following treatments: 1) 30 min of daily boar exposure, 2) 15 min of daily boar exposure, 3) 5 min of daily boar exposure, 4) continuous fence-line boar exposure, plus walked to a neutral pen and exposed to a different boar for 10 to 15 min daily, or 5) continuous fence-line boar exposure. Boar exposure lasted for 30 d. The percentage of gilts exhibiting first estrus by 210 d of age ranged from a high of 65.0 for treatment 4 to a low of 10.0 for treatment 5. Treatments 1, 3 and 4 were greater than treatment 5 (P less than .05), but not different from treatment 2. There were no differences in average age at first estrus. Treatment means for days to puberty after boar exposure were not different (P greater than .05). However, a significant treatment X season interaction occurred. This interaction appears to suggest seasonal trends. These results indicate that treatments 1 and 4 (30 min daily and continuous fence-line boar exposure plus 10 to 15 min, respectively) were the most effective methods tested for the induction of first estrus.

Animals↗

Control of luteinizing hormone in postpubertal boars with large testes.

The objective of the present study was to investigate endocrine control of LH in postpubertal boars with large testes. Eight boars with the highest estimated paired testis weights from a line selected for large testes and nine boars from a line selected at random were used. Blood samples were collected over a 13-h period at weekly intervals for 4 wk. Samples were collected at 12-min intervals for 12 h before and 1 h after exogenous LHRH. Boars were bled when they were intact during the initial week. The second and third blood collections were 7 and 14 d after castration. The fourth bleeding occurred 7 d after exogenous 17 beta-estradiol (E2) replacement. In intact boars, mean LH was similar between boars from the two groups, but amplitude of pulses of LH was lower in intact boars with large testes than in boars from the control line. Maximum concentration of LH after administration of LHRH was less in boars with large testes than in boars from the control group. Seven days after castration, characteristics of LH measured did not differ between males from the two groups. However, 14 d after castration, amplitude of pulses of LH and maximum concentrations of LH after LHRH were less in males from the group with large testes than in males from the control group. After E2 administration, amplitude of pulses of LH tended to be lower in males from the group with large testes than in males from the control group.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

[The effect of chorionic gonadotropin administration on testosterone levels in the blood of boars with sexual function disorders].

Thirty-three boars with sexual dysfunctions and twenty-six boars clinically sound as to their reproductive capacity were evaluated for the testosterone levels in the blood plasma before i.v. administration of 500 i.u. of chorionic gonadotropin and two hours after the administration. A group of animals with reproduction disorders comprised boars with an impaired quality of ejaculate and low fertility ability (18 boars) and with sexual dysfunctions (15 boars). No statistically significant difference in the basal concentration of testosterone in the blood was found in the boars with the studied sexual dysfunctions, as compared with the boars with no sexual dysfunctions. Administration of chorionic gonadotropin increased significantly the plasma testosterone levels in both groups. If the effect of chorionic gonadotropin on the studied level of this hormone was compared in boars with sexual dysfunctions and in boars without any disorders, no significant differences were proved. It has been inferred from the above findings that there are no significant disorders of androgen supply and incretion reserve of the gonads in the boars with sexual dysfunctions.

Animals↗

Physiology of the Meishan boar.

Onset of puberty (sperm production) occurs at a much younger age (56-84 days) in Meishans than in conventional boars (120-180 days). Throughout postnatal development, Meishans exhibit markedly higher (two- to ten-fold) concentrations of serum FSH, LH and androgens compared with conventional boars, and these high hormone concentrations are maintained at maturity. Increased gonadotrophin concentrations occur only in Meishan males, since concentrations in female Meishans and conventional females do not differ. In the Meishan boar, FSH increases steadily during establishment of sperm production and LH increases markedly after tubule diameter stabilizes, while FSH and LH concentrations are low and change little during this period of rapid testicular growth in conventional boars. The proportion of the testis occupied by Leydig cells is two-fold greater and average Leydig cell size is two- to four-fold larger in Meishans than in conventional boars during the onset of spermatogenesis and into maturity. Testis size in Meishans is only half that of conventional boars at maturity, and the number of Sertoli cells is markedly reduced in Meishans. However, Meishan testes exhibit reduced degeneration of germ cells and spermatids during spermatogenesis, and spermatogenic efficiency per Sertoli cell in Meishans is double that in conventional boars. At maturity, Meishan pituitaries have greater mass, larger gonadotrophs, higher content of FSH, and greater expression of genes for FSH and LH subunits than found in conventional boars. The high concentrations of serum gonadotrophins in the mature Meishan exhibit a typical postcastration rise, respond to GnRH stimulation and are suppressed by gonadal steroids, indicating that the hypothalamo-pituitary-gonadal axis functions normally but with much higher set points in Meishan boars. These unusual endocrine and physiological attributes in boars of the highly prolific Meishan breed offer a unique model for further investigation of factors influencing early onset of puberty and efficiency of male reproductive function.

Animals↗

Toxicity effects of latex gloves on boar spermatozoa.

It is known that several materials used in semen collection have been found to be detrimental to spermatozoal motility. In this study, examinations for toxic effects of latex and vinyl gloves, used with and without talcum powder on boar spermatozoa, were performed. Ten boars of known fertility with >/=80% sperm motility were divided into two groups (n = 5 boars each) for in vitro and in vivo studies. In the in vitro study, semen was collected from each of the five boars and was divided into five separate aliquots (5 ml each). One aliquot from each of the boars remained as the control, while the remaining aliquots were divided into individual treatments exposing the semen to a l cm(2) piece of latex or vinyl glove with or without talcum powder. In the in vivo experiment, semen from each of the five boars was collected using a gloved hand. During collection, the first half of the sperm-rich fraction was collected into a filtered sterile container, while the second half of the fraction was allowed to run through the palm of either a latex or vinyl powdered glove prior to collection in the container. In both experiments, semen sample motility was assessed by two independent observers at 1 minute after exposure. Results of both experiments consistently showed a significant (P<0.05) effect of latex gloves (with or without talcum powder) on boar semen when compared with the control semen. Motility was at or near 0% at 1 min after exposure to latex. No significant difference (P>0.05) in motility was observed between the control semen and the semen exposed to talcum powdered vinyl gloves. These results show that latex gloves are detrimental to boar spermatozoa. Therefore, it is suggested that when collecting boar semen vinyl gloves should be used.

Journal Article↗

Zona-penetration in vitro test for evaluating boar sperm fertility.

We investigated the capacity of porcine sperm-zona binding and penetration by using bioassay to differentiate between spermatozoa from fertile and subfertile boars. Semen was collected from Large White boars grouped into categories of fertile and subfertile (n=5 per each group) according to the results of artificial insemination. Boars in both groups showed similarly hyperactivated sperm motility at insemination (44.72 and 43.03% respectively) regardless of the lower percentage of progressive motility observed in the ejaculates of subfertile boars. At in vitro insemination, a high proportion of the sperm population (43.76%) in the subfertile boars was without acrosomes, while in the fertile boars this proportion was only 24.35%. The sperm penetration rate of fertile boars reached 66.03% while that of subfertile boars was only 25.08%. In conclusion, the results of our study showed that the penetration rate by boar spermatozoa of the zona pellucida can be used to predict fertility and/or as an in vitro standard for describing porcine semen characteristics.

Journal Article↗

Semen changes in boars after experimental infection with porcine reproductive and respiratory syndrome (PRRS) virus.

Eleven boars seronegative to porcine reproductive and respiratory syndrome virus (PRRSV) were trained for semen collection: five boars were inoculated intranasally with 6 x 10(6)TCID(50)/ml of PRRSV (Group A); four boars were inoculated intranasally with 6 x 10(4)TCID(50)/ml (Group B); and two boars were used as uninfected control (Group C). Semen samples were collected at 7-d intervals from 49 d prior to experimental inoculation with PRRSV to 70 d after inoculation, and were examined for sperm volume, sperm concentration, sperm morphology, sperm motility and for the presence of PRRSV. The infection in boars was demonstrated by the reisolation of PRRSV from the serum of all inoculated boars. Rectal temperatures and general health of the boars were clinically normal throughout the trial. Differences were observed in the quality of semen collected from boars after experimental infection with PRRSV. This infection induced a significant decrease in sperm motility and in spermatozoa with normal acrosomes. Of the semen samples tested for virus isolation in swine alveolar macrophages PRRSV was only isolated in 1 boar from Group B. The virus was detected in an additional semen sample in Group A by the production of an antibody titer in a biological assay. All attempts to detect PRRSV by RT-PCR in semen samples were unsuccessful. Nevertheless, from our study it is possible to suggest that the PRRSV can occasionally be transmitted in the semen during the initial phase of the disease.

Journal Article↗

Do different portions of the boar ejaculate vary in their ability to sustain cryopreservation?

Previous studies have shown sperm quality post-cryopreservation differs depending on the fraction of the seminal plasma boar spermatozoa are fortuitously contained in. As such, spermatozoa contained in the first 10 mL of the sperm-rich fraction (portion I) have better sustained handling procedures (extension, handling and freezing/thawing) than those contained in the ulterior part of a fractionated ejaculate (second portion of the sperm-rich fraction and the post-spermatic fraction, portion II). However, those studies were performed using pooled samples. In the present study, individual ejaculates were used. Split ejaculates (portions I and II) from five boars were frozen and thawed using a conventional freezing protocol, followed by computer-assisted motility and morphology analysis (CASA and ASMA, respectively), as well as an Annexin-V assay for spermatozoa from each boar and ejaculate portion. Significant differences between portions were observed in all ASMA-derived variables, except in one boar. Also significant differences were observed between boars and ejaculate portions in sperm quality post-thaw. We identified, however, boars showing best results of motility and sperm membrane integrity post-thaw in portion I, while in other boar the best results was observed in portion II. It is concluded that the identification of the ejaculate portion more suitable to sustain cryopreservation in each individual boar may be a readily applicable and easy technique to diminish variation in sperm freezability among boars.

Animals↗

Ixodid ticks parasitizing Iberian red deer (Cervus elaphus hispanicus) and European wild boar (Sus scrofa) from Spain: geographical and temporal distribution.

Commercial hunting of Spanish wild ungulates has made them an important economic resource. Wild ungulates may have an important role in the maintenance of ixodid tick populations, and also as reservoirs of pathogens. We studied the ixodid ticks that parasitize Iberian red deer and European wild boar from Spain. Ixodid ticks (n=6,336) were collected from 431 Iberian red deer and 142 wild boar in different regions of Spain. We found 10 different ixodid tick species parasitizing Iberian red deer, mainly Hyalomma marginatum marginatum (63.7%), Rhipicephalus (Boophilus) annulatus (7.9%) and R. bursa (7.5%). R. (Boophilus) annulatus was only collected in the province of Cádiz (southern Spain). We found 8 ixodid tick species on the wild boar, mainly Hy. m. marginatum (68.7%), R. bursa (14.6%) and Dermacentor marginatus (9.3%). We found one adult Hy. marginatum rufipes and one adult Hy. anatolicum excavatum parasitizing wild boar from south-central Spain. Mean prevalence of ixodid ticks was 41.3+/-0.08% (n=475) and 31+/-0.09% (n=284) and intensity of parasitization was 13.9+/-0.2 (n=283) and 13.6+/-0.3 (n=130) ticks/animal for Iberian red deer and wild boar, respectively. Only 5 of the 13 ixodid tick species found were shared by Iberian red deer and wild boar. This finding could indicate a host preference when Iberian red deer and wild boar share common habitats. In both Iberian red deer and wild boar from south-central Spain the monthly relative frequencies of Hy. m. marginatum and R. bursa presented an inverse pattern. The highest Hy. m. marginatum relative frequencies coincided with the lowest R. bursa relative frequencies along the year. R. bursa and I. ricinus were present in areas from northern to southern Spain while Hyalomma sp. and D. marginatus were exclusively collected in the two southern thirds of Spain. Haemaphysalis sp. and D. reticulatus were collected in northern Spain. Hy. m. marginatum and R. bursa were present during the whole year in red deer and wild boar from south-central Spain, showing more than one life cycle per year. These results are important for understanding the role of wild ungulates in the maintenance of tick infestations and to improve tick control programmes.

Animals↗

Lesions in the reproductive tract of boars experimentally infected with porcine rubulavirus.

"Blue eye" disease of pigs in Mexico is caused by porcine rubulavirus and characterized by infertility in sows and boars, nervous signs in young pigs, and corneal opacity in pigs of all ages. The pathogenesis of reproductive tract lesions in rubulavirus-infected boars has not previously been investigated. In a first experiment, four 9-month-old boars were inoculated with porcine rubulavirus and killed 5, 15, 30 or 45 days post-inoculation (pi). In a second experiment, four similar boars were inoculated with the same virus and two animals were killed on each of days 70 and 80 pi. Swelling of the head of the epididymis developed in all inoculated boars at approximately day 15 pi. Reduced spermatozoan motility and concentration were detected in semen samples collected from one boar from day 21 pi. At post-mortem examination, nodules were seen in the head of the epididymis of the boars killed 15, 30 or 45 days pi and the right testis of the pig killed 30 days pi was atrophic. Corresponding histopathological epididymal alterations included formation of spermatic granulomas and vacuolar degeneration of ductular epithelium. These lesions were associated with mononuclear cell infiltration and interstitial fibroplasia. Degeneration of seminiferous tubules and interstitial mononuclear cell infiltration were seen in the atrophic testis of the pig killed 30 days pi. There was fibrosis of the head of the epididymis in all boars killed 70 or 80 days pi and one of these animals also had right testicular atrophy associated with degeneration of seminiferous tubules, lymphocytic infiltration and giant cell formation. Porcine rubulavirus antigen was detected by immunofluorescence labelling in the head of the epididymis of the pigs killed 15, 30 or 45 days pi and in one animal killed on day 70 pi. These results indicate that porcine rubulavirus can cause severe epididymo-orchitis and reduced semen quality in sexually mature boars.

Animals↗

Impact of boar exposure on puberty attainment and breeding outcomes in gilts.

We examined the most effective method of boar exposure for the attainment of puberty in 89 gilts. At 160 days of age, we allocated gilts to daily direct contact with a vasectomized boar after movement of pen groups of gilts to a detection-mating area (DGB: n = 30); daily direct contact with boars in the gilt home pens (DBG: n = 31); or daily fenceline contact between boars and gilts housed in individual gilt stalls (FBG: n = 28). DGB gilts were younger (P < or = 0.05) than FBG gilts at puberty. Direct boar contact reduced the interval from initial boar contact to puberty in DGB and DBG gilts, compared to fenceline contact in FBG gilts (P < 0.05). There was no difference (P > or = 0.05) between treatment for pubertal weight, backfat, lifetime growth rate, or duration of first pubertal estrus. Backfat depth and leptin concentration at 160 days of age were positively correlated (P < or = 0.05). We detected no relationships between leptin or IGF-1 concentration at 160 days of age and the interval from initial exposure to a vasectomized boar to puberty (P > 0.05). Based on objective criteria, fenceline contact with a boar (BC) during artificial insemination improved the quality of artificial insemination compared to no boar contact (NC) (P < 0.05).

Adipose Tissue↗

The effect of repeated boar exposure on cortisol secretion and reproduction in gilts.

It has been proposed that short-term activation of the hypothalamo-pituitary adrenal axis, with a consequent increase in the secretion of cortisol, amy disrupt the endocrine events prior to ovulation and thereby impair reproduction in females. We investigated this concept in gilts in which oestrus was detected by introduction to boars, where intense physical contact is possible, or by applying pressure to the back of gilts (back-pressure test) during fence-line exposure to boars, where intense physical contact is prohibited. We expected that there would be a greater release of cortisol and that reproduction would be inhibited in gilts introduced to boars compared to gilts in which the back-pressure test was used. As expected, introduction of gilts to boars resulted in a significant transient increase in plasma concentrations of cortisol while there was no significant effect of using the back-pressure test on plasma cortisol. Nevertheless, introduction of gilts to boars did not impair reproduction and there was no effect of method of detecting oestrus on duration of oestrus, sexual receptivity, fertility or fecundity. The length of the oestrous cycle was decreased and ovulation rate increased in gilts that were introduced to boars compared to gilts that underwent the back-pressure test, indicating that introduction of gilts to boars may have stimulated these aspects of reproduction. These stimulatory effects may have been due to an increased exposure of gilts to sexual behaviour and stimuli from boars when introduced to boars and/or to stimulatory effects of the hypothalamo-pituitary adrenal axis on some aspects of reproduction.

Adrenal Glands↗

Effects of age and live weight on fat 5 alpha-androstenone levels in young boars fed two planes of nutrition.

The aim of the present experiment was to determine whether age, live weight, or a combination of both, was the most important factor influencing fat 5 alpha-androstenone levels in male pigs. Three groups of 50 boars each were fed either on a liberal plane of nutrition (CTRL group) or were restricted (SW and SA groups). Fat 5 alpha-androstenone was measured three times in each pig (on biopsies at two different times and at slaughter) at either the same live weight (SW) or at the same age (SA) as CTRL boars. In addition, the genital tract was dissected at slaughter. SW boars (aged 169 days) exhibited higher fat 5 alpha-androstenone levels than CTRL boars (aged 139 days) when the first biopsy was taken at 80 kg of live weight (1.2 vs 0.8 microgram/g; P less than 0.05). By the time of the second biopsy (100 kg of live weight) and at slaughter (125 kg) there was no significant difference between the SW and CTRL groups, although the SW were 43-55 days older than the CTRL. At all three measurement times, fat 5 alpha-androstenone was lower in SA than in CTRL boars which were 21-36 kg heavier (0.5 vs 0.8 micrograms/g at 139 days; 0.9 vs 1.3 micrograms/g at 160 days; 1.2 vs 2.0 micrograms/g at 185 days; P less than 0.001). Partial correlations between fat 5 alpha-androstenone and age were significant at the first biopsy, whereas partial correlations with live weight were significant at all three times of measurement. In SA boars weighing 90 kg there was a significant correlation between fat 5 alpha-androstenone and all the developmental traits of the genital tract. In SW and CTRL pigs weighing 125 kg, fat 5 alpha-androstenone was significantly correlated with accessory sex gland development but not with testis or epididymis weight. From the present data it is concluded that both age and live weight had a significant effect on fat 5 alpha-androstenone levels in young, light boars. In older, heavier boars, age had no effect per se but live weight still had a significant influence on 5 alpha-androstenone concentrations. In boars weighing 90 kg, fat 5 alpha-androstenone level depended on sexual maturity. When the animals were sexually mature at 125 kg of live weight, 5 alpha-androstenone level depended on the individual's potentiality for steroid production, which is probably under genetic control.

Adipose Tissue↗

Characterization of 11beta-hydroxysteroid dehydrogenase activity in testicular tissue of control and GnRH-immunized boars as a possible regulator of spermatogenesis.

Glucocorticoids are involved in the regulation of spermatogenesis in the boar testis by initiating apoptosis in early stages of germ cell development. Because cortisol activity is modulated by the 11beta-hydroxysteroid dehydrogenase system (11beta-HSD), the present study determined both 11beta-activating (reductive) and inactivating (oxidative) enzyme activities in testicular tissue preparations of control boars (n = 5), GnRH-immunized boars (n = 5), and immunized, estradiol-infused boars (n = 6) by radioenzyme assay based on the conversion of tritiated cortisol to cortisone in the presence of NAD+ (inactivation) or tritiated cortisone to cortisol in the presence of NADPH (activation). The presence of both isoforms, 11beta-HSD 1 and 11beta-HSD 2, was confirmed by RTPCR in testicular tissue of control boars. Additionally, cortisol, testosterone, estradiol, and LH were determined in blood plasma sampled twice before killing. Immunization led to a drop of LH from 4.3 +/- 0.3 pmol/L to 1.0 +/- 0.3 pmol/L (testosterone: 11.63 +/- 0.83 nmol/L vs. 0.28 +/- 0.07 nmol/L; 17beta-estradiol: 512.61 +/- 47.60 pmol/L vs. 77.05 +/- 14.00 pmol/L). Low 11beta-HSD reductive activity was found in boars (1 pmol steroid x min (-1) x mg (-1)). It decreased to trace amounts in immunized boars (0.07 pmol steroid x min (-1) x mg (-1)). Oxidative activity was found in boars with 10.19 +/- 2.28 pmol steroid x min (-1) x mg (-1) protein. Immunization led to a sharp decrease (0.08 +/- 0.03 pmol x min (-1) x mg (-1)). Infusion of 17beta-estradiol significantly elevated peripheral estradiol concentrations to 752.07 +/- 24.19 pmol/L which still is a physiological concentration in this species. The infusion led to a minimal reductive activity (0.04 pmol steroid x min (-1) x mg (-1)), but led to a 6-fold rise of the 11beta-HSD oxidative activity to 0.47 +/- 0.14 pmol x min (-1) x mg (-1) compared to immunized boars. It is concluded that the 11beta-HSD system is involved in the regulation of cortisol activity in the testis and thus in the regulation of spermatogenesis.

11-beta-Hydroxysteroid Dehydrogenase Type 1↗

Sertoli cells in the boar testis: changes during development and compensatory hypertrophy after hemicastration at different ages.

Changes in Sertoli cell numbers and testicular structure during normal development and compensatory hypertrophy were assessed in crossbred Meishan x White Composite males. Boars were assigned at birth to unilateral castration at 1, 10, 56, or 112 days or to remain as intact controls through 220 days. The first testes removed were compared to assess testicular development. At 220 days, testicular structure was evaluated in boars representing the 25% with the largest (Lg) testis and the 25% with the smallest (Sm) testis in each treatment group. The number of Sertoli cells per testis reached a maximum by Day 56 in Sm testis but not until Day 112 in Lg testis boars, indicating a longer duration of Sertoli cell proliferation in Lg testis boars. Unilateral castration of Lg testis boars on Days 1, 10, 56, and 112 caused the weight of the remaining testis to hypertrophy by 149%, 135%, 119%, and 120%, respectively, and total sperm production to increase to 127%, 128%, 97%, and 106%, respectively. However, Sertoli cell numbers changed little in hemicastrate boars. In Lg testis boars, compensatory hypertrophy primarily involved proliferation of Leydig cells and expansion of existing Sertoli cells with little increase in Sertoli cell numbers, but in Sm testis boars, it involved expansion of existing Leydig and Sertoli cells without increase in cell numbers. These results indicate that Lg and Sm testis boars display intriguing differences during both development and compensatory hypertrophy, and they identify a unique animal model for further studies of factors that program and control Sertoli cell proliferation.

Age Factors↗

An analysis of leg abnormalities of boars in the Queensland performance testing station.

An analysis was made of the results of leg inspections of boars in the Queensland boar testing station at the start and end of their performance tests. The frequency among boars of 12 specific faults ranged from zero to 90% at the start and 7% to 73% and the end of testing. Of the 362 boars examined, 20% suffered from leg weakness. 11% of these had to be slaughtered and 9% recovered after return to the farm. The only faults significantly associated with leg weakness were: "up on toes" of the front feet and excessive flexion of the front knees ("over at knee"). The sire, breed and herd of origin of a boar had little effect on its having any one of the 12 faults. However, herds were found to differ in the total number of faults per boar and Large White had more front leg faults than Landrace. The correlation between number of leg faults and growth rate of a boar during test was + 0.12. Although lef weakness was an important cause of boar wastage, neither it nor leg faults were significant sources of error in evaluating the performance of boars which completed testing.

Animals↗