Growth of the conceptus in alpacas.

OBJECTIVE: To determine growth of the alpaca conceptus during early gestation, using ultrasonography. ANIMALS: 40 pregnant alpacas (20 multiparous, 20 nulliparous). PROCEDURE: Transrectal ultrasonography with a 5-MHz probe was performed 3 times weekly from days 7 through 45 after copulation (day of copulation = day 0). Blood samples were collected for progesterone assay on days of ultrasonography. RESULTS: Forty embryonic vesicles and embryos were identified and measured. Embryonic vesicles were first detected on day 12 after copulation and appeared spherical. Cumulative percentage of embryonic vesicles detected was 50, 82.5, and 100% on days 12, 14, and 16, respectively. Embryos were first detected by day 22 and heartbeats by day 24. Similarly, cumulative percentage of embryos detected was 17.5, 82.5 and 100% for 22, 24, and 26 days after copulation, respectively. Embryonic vesicles occupied both uterine horns beginning on day 19. A positive correlation existed between length and width of embryonic vesicles. Size of embryonic vesicles and embryos and progesterone concentrations did not differ between multiparous and nulliparous females. Five sets of twins were detected from days 21 through 33 after copulation, but the conceptus identified in the right uterine horn became nondetectable between days 28 and 33. CONCLUSIONS AND CLINICAL RELEVANCE: Ultrasonography was useful in detecting the earliest appearance of alpaca embryonic vesicles and determining the changes in growth from days 12 through 45 after copulation. Embryos were first detected by day 22. Transrectal ultrasonography was not harmful to animals and did not provoke embryonic death in this study.

Reproductive aspects and storage of semen in camelidae.

The characteristics of male and female reproductive tracts and reproductive physiology in camelids are described. An account is given on methods of collection, characteristics and storage of semen, and fertility after artificial insemination (AI) with fresh, liquid-stored and frozen-thawed lamoid and camel semen.

Degelification of alpaca semen and the effect of dilution rates on artificial insemination outcome.

Degelification of highly viscous alpaca semen was attempted using two enzymes: trypsin and collagenase. Dilution effect on artificial insemination was determined in alpacas. Semen from 4 male alpacas was collected, degelified, diluted, and inseminated into 80 female alpacas. Degelification was achieved adding trypsin and collagenase enzymes to fresh semen samples. Semen was diluted with egg-yolk glucose citrate to give concentrations of 4, 8, and 12 million spermatozoa/mL. Females were induced to ovulate with human chorionic gonadotropin and then inseminated deep into the uterine horns. Analysis of variance was used to determine differences in the effect of trypsin and collagenase on sperm acrosome and on motility and live spermatozoa. The chi-square test was used to determine differences in pregnancy of artificially inseminated females. Semen was degelified with different concentrations of trypsin and collagenase. There were differences (p < .05) in the pregnancy rate of female alpacas inseminated with 4 million (53.3%), 8 million (66.7%), and 12 million sperm/mL (61.5%). Alpaca semen may be degelified using trypsin and/or collagenase. It seems that 8 million sperm/mL is adequate for artificial insemination in alpacas.

Effect of repeated collection on semen characteristics of alpacas.

Semen characteristics of alpacas were studied after repeated collections. Twelve adult males were divided into three groups of four each for semen collection once, twice, or three times every other day. The duration of copulation; volume of ejaculate; pH; motility; sperm concentration (number of sperm/milliliter semen); total number of sperm per ejaculate; and percentages of live, normal, and abnormal spermatozoa were analyzed by regression analysis. Semen color and consistency were analyzed by the chi-square test. Between the first, second, and third ejaculations, there were differences (p < 0.05) in sperm concentration; percentages of normal spermatozoa and abnormal spermatozoa; sperm with abnormal heads and abnormal tails; and consistency (viscous, viscous, and semi-viscous). There were no differences (p > 0.05) in ejaculated volume, percentage of live spermatozoa, pH, percentage of cytoplasmic droplets, and duration of copulation. Some males from which semen was collected on the three-mating schedule ejaculated only seminal plasma during the second and third copulation starting on Day 10 of the study. There were differences between males (p < 0.05) for most of the characteristics studied. In sum, frequency of mating affected some semen characteristics that may be important determinants of the fertility of male alpacas.

Collection of semen and artificial insemination of alpacas.

Semen collection and artificial insemination have not yet been fully developed in the alpaca. Thus, we collected semen from 7 males using a modified artificial vagina placed inside a dummy. Forty adult female alpacas, previously induced to ovulate with hCG, were artificially inseminated with fresh undiluted semen by laparoscopy or by cervix. The Chisquare test was used to determine differences in the fertility rate of the 2 insemination methods. The mean duration of copulation, semen volume, sperm concentration and the percentages of live spermatozoa and normal spermatozoa were 21.6 min, 1.9 ml. 147,500/mm(3), 69.6% and 75.9%, respectively. There were 6.7% abnormal heads, 12.3% abnormal tails and 3.8% cytoplasmic droplets. The consistency of semen was viscous and formed a coagulum. The pH was 7.2, and the semen was milky white in color. The duration of copulation was comparable to natural copulation, and semen characteristics reflected those of the natural ejaculate. The percentage of pregnancy was 68%, with no differences due to method of semen deposition (laparoscopy, 67%; cervix, 73%).

Induction of parturition in alpacas and subsequent survival of neonates.

OBJECTIVE: To evaluate use of fluprostenol, dexamethasone, and oxytocin for induction of parturition in alpacas, and to determine viability of the newborn crias. DESIGN: Prospective, randomized, controlled trial. ANIMALS: 36 pregnant alpacas within 10 days of parturition. PROCEDURE: Animals were randomly assigned to treatment groups. Plasma progesterone and plasma and urine estrone sulfate concentrations were measured for 5 days after treatment. Clinical signs of the neonates were determined. RESULTS: Time between treatment and parturition was significantly shorter for animals that received fluprostenol than for animals in any other group. The highest dose of dexamethasone (0.5 mg) caused fetal death. None of the other treatments induced early parturition. Time between birth and first suckling, body weight, rectal temperature, pulse rate, and respiratory rate at birth and serum IgG concentration 24 hours after birth were not different between crias born after fluprostenol treatment and crias born to control alpacas. CLINICAL IMPLICATIONS: Fluprostenol was effective at inducing parturition in these alpacas, but dexamethasone and oxytocin were not. Crias born after fluprostenol treatment were similar to crias born to control alpacas.

Hormonal indicators of pregnancy in llamas and alpacas.

OBJECTIVE: To determine concentrations of estrone sulfate in serum, estrone sulfate in urine, relaxin in serum, and progesterone in serum in pregnant llamas and alpacas and to assess the potential of these hormones as pregnancy indicators. DESIGN: Prospective study. ANIMALS: 19 parous pregnant camelids (8 llamas and 11 alpacas). PROCEDURE: Estrone sulfate concentrations (in serum and in urine) and progesterone concentrations (in serum) were determined by enzyme immunoassay. Relaxin concentrations (in serum) were measured by radioimmunoassay. Serum and urine samples were collected daily for the first 30 days after breeding and, thereafter, once weekly until parturition. RESULTS: Estrone sulfate concentrations (in serum and in urine) peaked twice during pregnancy. The first took place 21 days after breeding and the second during the last month of pregnancy. Relaxin concentrations increased at 3 months of gestation to > 20 ng/mL, decreased at 5 months to 5 ng/mL, then increased from 8 months of pregnancy until parturition. Progesterone concentrations were detectable 4 days after breeding and were maintained > 2 ng/mL throughout pregnancy. CLINICAL IMPLICATIONS: The first increase in estrone sulfate concentration over basal values may indicate early interaction between mother and embryo, whereas the second increase may reflect fetal viability. Use of estrone sulfate concentration to diagnose pregnancy in llamas and alpacas is highly dependent on time of sampling. Relaxin concentration in serum is a superior indicator of pregnancy after the second month in the Ilama and alpaca because its existence is suggestive of interaction between mother and fetus, and concentrations are greater than basal values for a long period of pregnancy. Progesterone is not a direct product of the embryo or fetus and only indirectly confirms a diagnosis of pregnancy.

In situ observation of the ovaries of llamas and alpacas by use of a laparoscopic technique.

A laparoscopic technique was used to observe in situ the ovaries of llamas and alpacas. Use of this technique results in minimal surgical stress and allows repetitive observation of various reproductive stages in the same animal. Ovarian follicular activity before and after breeding, time of ovulation, corpus luteum formation and regression, early embryo death, failure of ovulation, and the early events of pregnancy can be assessed quickly and safely. For 1,291 laparoscopies performed, postsurgical disturbance was not observed, and animals were released from the clinic 1 hour after laparoscopy.

Evaluation of intra-abdominal vasectomy in llamas and alpacas.

A method of intra-abdominal vasectomy (deferentectomy), using a laparoscopic technique in llamas and alpacas, was evaluated. Food was withheld from 14 animals for 24 hours before sedation and laparoscopy. The ductus deferens was located close to the bladder, and a 2- to 3-cm section of ductus deferens was resected with the aid of a pair of hook scissors. The procedure was completed in 5 to 8 minutes, and animals did not have any adverse effects. Forty-five days after vasectomy, animals were used for detecting sexually receptive females or inducing ovulation during reproductive physiologic studies. The procedure did not impair libido and had no effect on male sexual behavior for many years. The technique is simpler, safer, and faster than the traditional external approach.