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Eazi breed cidr

Manufactured by Zoetis
Sourced in United States, China

Eazi-Breed CIDR is a controlled internal drug release device used to synchronize estrus and breeding in cattle, sheep, and goats. It is a small, T-shaped device that is inserted into the animal's vagina and releases a controlled amount of progesterone over time.

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14 protocols using eazi breed cidr

1

Synchronizing Estrus for Embryo Transfer

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Recipient estrus synchronization was initiated by inserting an intravaginal progesterone device (1.38 g; Eazi-Breed CIDR; Zoetis) and intramuscular administration of gonadotropin (100 mcg; Factrel; Zoetis) on day 0 (sixteen days prior to transfer). On day 7, the CIDR was removed and intramuscular prostaglandin (25 mg; Lutalyse; Zoetis) was administered. Recipients were monitored for estrus, and a second intramuscular dose of gonadotropin (100 mcg; Factrel; Zoetis) was administered on day 9. Prior to transfer on day 16, recipient response to synchronization was confirmed via detection of an appropriate corpus luteum with transrectal ultrasonography. Prior to transfer, each recipient received a caudal epidural using 100 mg 2% lidocaine (Xylocaine; Fresenius). Embryos were transferred via non-surgical, transcervical technique, and the blastocyst was deposited into the uterine horn ipsilateral to the corpus luteum. Pregnancy was diagnosed on day 35 of embryonic development by transrectal ultrasonography (5.0 MHz linear probe; EVO Ibex, E.I. Medical Imaging).
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2

Embryo Transfer and Hormone Treatments in Cows

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The study was approved by the Institutional Animal Care and Use Committee of  Mississippi  State University (11-023) and implemented at The Coastal Plain Branch Experiment Station of Mississippi State University in Newton, MS in the Spring of 2011. Lactating Angus crossbred cows were synchronized for estrous by receiving a CIDR (Eazi-Breed CIDR; Zoetis, Madison NJ) for 7 d. One d after removal, all cows (n = 62) received an injection of PGF2α (25 mg IM; Lutalyse; Zoetis). Cows were observed for estrus (d 0) four times per d (1 h at each time) during the 80 h post-PGF2α. Following manual evaluation of the CL via palpation per rectum, all cows exhibiting estrus with a CL received an embryo in the uterine horn ipsilateral to the CL on 7 d after estrus. At the time of transfer, cows were assigned to 1 of 4 treatments: no further treatment (Control, n = 16), a CIDR insert (CIDR, n = 16), an injection of hCG (1000 IU, IM; Sioux Biochemical, Inc, Sioux Center, IA; hCG, n = 15) or an injection of GnRH (100 μg, IM; Cystorelin; Merial, Duluth, GA; GnRH, n = 15).
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3

Estrus Synchronization in Angus Heifers

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Virgin Angus heifers across two different years (year 1, n = 38; year 2, n = 28; total n = 66) during the month of April and located at a University of Tennessee AgResearch and Education Center were grazed on mixed grass pastures and had ad libitum access to hay. Average heifer age was 1.2 ± 0.1 yr. Estrus was synchronized according to Figure 1A and defined as the time when a heifer first stood to be mounted by another. Depending on the year, prostaglandin F (PGF) administered was dinoprost tromethamine (25 mg i.m.; Lutalyse, Zoetis, Parsippany, NJ, USA) or cloprostenol (500 μg i.m., Estrumate, Merck, Rahway, NJ, USA). Eleven days later, gonadotropin-releasing hormone (GnRH) was administered (100 μg i.m., gonadorelin hydrochloride, Factrel, Zoetis or 100 μg i.m., gonadorelin diacetate tetrahydrate, Cystorelin, Boehringer Ingelheim, Duluth, GA, USA). A controlled internal drug release (CIDR) device was placed intravaginally (1.38 g progesterone, Eazi-Breed CIDR, Zoetis). Seven days later, the CIDR was removed, PGF was administered, and an iButton that had been previously affixed to a blank CIDR (containing no progesterone) was placed intravaginally. Beginning ~24 h after PGF, estrus activity was visually assessed hourly until the first heifer displayed signs of estrus at which point monitoring was continuous by a team of individuals on a rotating schedule.
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4

Bovine Embryo Transfer via Estrus Synchronization

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Estrus synchronization of recipient cattle began 16 days prior to the embryo transfer with the use of an intravaginal progesterone releasing device (1.38 g; Eazi-Breed CIDR; Zoetis) and the administration of gonadorelin (100 mcg; Factrel; Zoetis) done on day 0. On day 7, the CIDR was removed and prostaglandin (25 mg; Lutalyse; Zoetis) was administered. A second dose of gonadorelin (100 mcg; Factrel; Zoetis) was given on day 9 and recipients were monitored for signs of estrus. Confirmation of recipient synchronization was done on day 15 via corpus luteum detection using a transrectal ultrasound. On day 16, embryo transfers were performed. Recipients received a caudal epidural of 100 mg 2% lidocaine (Xylocaine; Fresenius) prior to embryo transfer. Two to three blastocysts were loaded into 0.25 cc straws and transferred using the non-surgical transcervical technique into the uterine horn ipsilateral to the corpus luteum. On day 35 of gestation, transrectal ultrasonography (5.0 MHz linear probe; EVO Ibex, E.I. Medical Imaging) was done to confirm pregnancies, and reconfirmed on day 80. A total of four embryo transfers were performed, and recipients were resynchronized for subsequent embryo transfers if they did not become pregnant from prior embryo transfers.
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5

Synchronization and hCG Treatments in Dairy Cows

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Cows between 39 and 64 DIM (mean ± SD = 45.2 ± 6.0) were submitted to a pretreatment for synchronization of ovulation, consisting of an Ovsynch + controlled internal drug-release insert (CIDR; Figure 1; Pursley et al., 1995) (link). Briefly, cows received GnRH (200 µg i.m.; Factrel, Zoetis) and a P4 intravaginal insert (Eazi-Breed CIDR; Zoetis). Seven days later, the P4 insert was removed, and prostaglandin F 2α (PGF 2α 25 mg i.m.; Lutalyse HighCon, Zoetis) was administered, followed by another PGF 2α 1 d later and a second GnRH 1 d after the second PGF 2α . Only synchronized cows with complete CL regression 2 d after PGF 2α (serum P4 < 1.0 ng/mL) and ovulation by 2 d after the last GnRH were used in the study (n = 64). The last GnRH of pretreatment was considered d 0 of the estrous cycle. After confirmation of synchronization, cows were randomly assigned to one of 3 treatments. Control cows (n = 22) did not receive any treatment except the synchronization protocol. Cows enrolled in the second treatment group (hCG7; n = 20) received an i.m. treatment with 3,300 IU of hCG (Chorulon, Merck Animal Health) 7 d after the last GnRH (d 7 of the cycle), and cows enrolled in the third treatment group (hCG7+13; n = 22) received 2 hCG treatments with 3,300 IU, one on d 7 and a second on d 13 after the last GnRH (d 7 and d 13 of the estrous cycle).
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6

Monitoring Physiological Responses to LPS Challenge

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Body temperature was recorded continuously at 1-min intervals starting 1 h before LPS challenge until 24 h after the start of challenge using a HOBO external temperature data logger (HOBO MX2304, Onset Computer Cooperation) with an external sensor probe that was mounted to a blank intravaginal cattle insert (Eazi-Breed CIDR, Zoetis). At 0, 1, 2, 3, 4, 6, 8, 12, and 24 h relative to the start of LPS challenge, heart rate, respiratory rate, and rumen motility were recorded. Heart rate and respiratory rate were determined by auscultation of the heart using a stethoscope and by observation of flank movement, respectively. Rumen motility was determined by auscultation in the left paralumbar fossa and recorded as rumen contractions counted in a 2-min interval. Rumination data were collected from a subset of animals (CTRL, n = 4; IVCa, n = 6) equipped with ear tag monitors (SMARTBOW, Zoetis) in 1-h intervals.
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7

Timed Artificial Insemination in Nulliparous Heifers

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A total of 12 nulliparous cycling Holstein heifers were randomly assigned (six heifers per treatment) to one of two treatments:

4‐day CoSynch+CIDR (n = 6): The heifers received an intravaginal CIDR insert (Eazi‐Breed CIDR®, Zoetis Animal Health, Florham Park, NJ, USA) containing 1.38 g of progesterone for 4 days. On the day of CIDR insert removal, 25 mg of PGF2α (5 mL Lutalyse ® Zoetis Animal Health) was injected IM; 72 h after CIDR insert removal, the heifers received 100 μg of GnRH (2 mL Factrel®, Zoetis Animal Health) IM and TAI (Fig. 1).

5‐day CoSynch+CIDR (n = 6): The heifers received an intravaginal CIDR insert containing 1.38 g of P4 for 5 days. The heifers were administered 25 mg of PGF IM at the time of CIDR insert removal, and 100 μg of GnRH IM and TAI 72 h after CIDR insert removal (Fig. 1).

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8

Lamb Rearing and Milking Protocol

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From the time of arrival at Keeble farm, the ewes were managed as a single flock under commercial grazing conditions. For breeding, ewes were progesterone-synchronised by inserting a controlled release intravaginal device (Eazi-Breed CIDR®, Zoetis New Zealand) on 13 March 2019 for a period of 12 days. Pregnancy diagnosis was undertaken twice in mid-pregnancy (4 June and 25 July) using trans-abdominal ultrasonography undertaken by a commercial operator to confirm pregnancy and foetus numbers. Single and twin-bearing ewes were retained while non-pregnant and triplet-bearing ewes were culled (n = 21).
On 30 July 2019, all ewes were weighed, body condition scored, and moved to a single paddock closer to the milking parlour with a pasture requirement according to commercial conditions for late pregnant ewes (pre-lambing). Forty-eight ewes were retained for lambing and the lambing period occurred between 13 August and 9 September 2019. On milking days (see below), lambs were separated from their dams for six hours between morning and afternoon milkings, during which time each lamb was bottle-fed 300 g of ewe’s milk [37 (link)]. If a ewe produced less than 1200 g/day of milk or abandoned their lamb/s, the lamb/s was/were removed from the ewe and fostered. These ewes, and ewes for whom all their lambs died (18), were excluded from the milking study.
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9

Cryotop Embryo Cryopreservation Protocol

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Unless otherwise indicated, chemicals were purchased from Sigma–Aldrich (St. Louis, MO, United States). The Cryotop devices were purchased from Ingamed (Maringá, Paraná, Brazil). Follicle-Stimulating Hormone (FSH), Pregnant Mare Serum Gonadotropin (PMSG), and Prostaglandin (PG) were purchased from Sansheng biological technology (Ningbo, China); EAZI-BREED-CIDR and Holding medium were purchased from Zoetis (New Jersey, United States).
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10

Cryotop Embryo Cryopreservation Protocol

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Unless otherwise indicated, chemicals were purchased from Sigma–Aldrich (St. Louis, MO, United States). The Cryotop devices were purchased from Ingamed (Maringá, Paraná, Brazil). Follicle-Stimulating Hormone (FSH), Pregnant Mare Serum Gonadotropin (PMSG), and Prostaglandin (PG) were purchased from Sansheng biological technology (Ningbo, China); EAZI-BREED-CIDR and Holding medium were purchased from Zoetis (New Jersey, United States).
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