MF Treatments Research Articles

The effect of follicle age on pregnancy rate in beef cows1

The effect of the age of the ovulatory follicle on fertility in beef cows was investigated. Multiparous (n = 171) and primiparous (n = 129) postpartum beef cows in 2 groups (G1 and G2) received estradiol benzoate (EB; 1 mg/500 kg BW, intramuscular [i.m.]) 5.5 d (G1; n = 162) and 6.5 d (G2; n = 138) after the final GnRH of a synchronization program (5d CO-Synch + CIDR) to induce emergence of a new follicular wave (NFW), followed by prostaglandin F2α (PGF(2α); 25 mg, i.m.) administration either 5.5 d ("young" follicle, YF; n = 155) or 9.5 d ("mature" follicle, MF; n = 145) after EB. Estrous detection coupled with AI 12 h later (estrus-AI) was performed for 60 h (MF) and 84 h (YF) after PGF(2α); cows not detected in estrus within this period received timed AI (TAI) coupled with GnRH at 72 and 96 h, respectively. Within the first 72 h after PGF(2α), more (P < 0.01) cows in the MF (76.3%) than YF treatment (47.7%) exhibited estrus, but through 96 h, the proportion detected in estrus (P < 0.05) and interval from PGF(2α) to estrus (P < 0.01) were greater in the YF than MF treatment (88.6% vs. 76.3%, 78.9 ± 0.8 vs. 57.5 ± 1.6 h, respectively). Age of the ovulatory follicle at AI was greater (P < 0.01) in the MF (9.32 ± 0.04 d) than YF (6.26 ± 0.02 d) treatment, but follicle diameter at AI and pregnancy rates did not differ between MF (13.1 ± 0.2 mm; 72.0%) and YF (12.9 ± 0.1 mm; 67.1%) treatments. Regardless of treatment, the diameter of the ovulatory follicle at AI and pregnancy rate were greater (P < 0.01) with estrus-AI (13.1 ± 0.1 mm; 75.0%) than TAI (12.6 ± 0.2 mm; 55.4%). Cows in the MF treatment that initiated a second NFW after EB but before PGF(2α) (MF2; n = 47) were induced to ovulate with GnRH and TAI at 72h, when ovulatory follicles were 4 d old and 10.2 ± 0.2 mm in diameter. Pregnancy rate for TAI (51.1%) in MF2 did not differ from TAI pregnancy rate (55.4%) across the MF and YF treatments. In summary, the age of the ovulatory follicle affected interval to estrus and AI but did not influence pregnancy rate in suckled beef cows.

Effect of follicle age on conception rate in beef heifers1

The objective of this study was to determine the effect of age of the ovulatory follicle on fertility in beef heifers. Ovulation was synchronized with the 5 d CO-Synch + controlled intravaginal drug release (CIDR) program in heifers in Montana (MT; n = 162, Hereford and Angus Crossbred) and Ohio (OH; n = 170, Angus Crossbred). All heifers received estradiol benzoate (EB; 1 mg/500 kg BW, [i.m.]) 6 d after the final GnRH of the synchronization program to induce follicular atresia and emergence of a new follicular wave (NFW) followed by prostaglandin F2α (PGF(2α); 25 mg, i.m.) administration either 5 d ("young" follicle [YF]; n = 158) or 9 d ("mature" follicle [MF]; n = 174) after EB. Estrous detection was performed for 5 d after PGF(2α) with AI approximately 12 h after onset of estrus. Ovarian ultrasonography (MT location only) was performed in YF and MF at EB, 5 d after EB, PGF(2α), and AI. Heifers in MT (n = 20) and OH (n = 18) that were not presynchronized or did not initiate a NFW were excluded from further analyses, resulting in 142 and 152 heifers in MT and OH, respectively. Heifers from the MF treatment in MT that initiated a second NFW after EB but before PGF(2α) (MF2; n = 14) were excluded from the primary analysis. In the secondary analysis, the MF2 group was compared to MF and YF treatments in MT. Estrous response was similar (90%; 252/280) between treatments and locations. Proestrus interval (from PGF(2α) to estrus) and age of the ovulatory follicle at AI were similar for MF heifers between locations (54.6 ± 1.7 h and 8.3 ± 0.07 h) but were greater (P < 0.01) for YF heifers in OH (78.5 ± 1.4 h and 5.3 ± 0.06 h) than MT (67.4 ± 1.6 h and 4.8 ± 0.06 h; treatment × location, P < 0.01). However, conception rate did not differ for MF (63.8%; 74/116) and YF (67.0%; 91/136) treatments. In the MT heifers, follicle size and follicle age at AI in the YF treatment (10.4 ± 0.15 mm and 4.8 ± 0.06 d, respectively) was less (P < 0.01) than in the MF treatment (11.0 ± 0.18 mm and 8.3 ± 0.11 d, respectively), but conception rate to AI did not differ between treatments in MT. In the MF2 group proestrus interval was greater (P < 0.01); hence, diameter of the ovulatory follicle and age were similar to that for the YF treatment. Conception rate to AI did not differ between MF2, MF, and YF (61.5, 63.3, and 64.7%, respectively) in MT. In conclusion, manipulation of age of the nonpersistent ovulatory follicle at spontaneous ovulation did not influence conception rate.

Metformin Impairs Vascular Endothelial Recovery After Stent Placement in the Setting of Locally Eluted Mammalian Target of Rapamycin Inhibitors Via S6 Kinase-Dependent Inhibition of Cell Proliferation

This study sought to examine the effect of oral metformin (Mf) therapy on endothelialization in the setting of drug-eluting stents (DES). Mf is a commonly used therapy in diabetic patients receiving DES. Mf and locally eluted mammalian target of rapamycin (mTOR) inhibitors used in DES have convergent molecular signaling; however, the impact of this drug interaction on stent endothelialization is unknown. We examined human endothelial aortic cells (HAECs) and a rabbit model of stenting to determine points on molecular convergence between these 2 agents and their impact on stent endothelialization. Western blotting of HAECs treated with Mf and the mTOR inhibitor sirolimus and 14-day rabbit iliacs treated with the combination of zotarolimus-eluting stents (ZES) and oral Mf demonstrated greater inhibition of S6 kinase (S6K), a downstream effector of mTOR complex 1, than either treatment alone. HAEC proliferation was significantly inhibited by Mf or sirolimus treatments alone and further reduced when they were combined. Knockdown of S6K via short interfering RNA in HAECs impaired cell proliferation via a cyclin D1-dependent mechanism, whereas its overexpression rescued the antiproliferative effects of both agents. Last, endothelialization and endothelial cell proliferation at 14 days were assessed in rabbits receiving ZES or bare-metal stents and Mf or placebo by scanning electron microscopy and bromodeoxyuridine/CD31 labeling, respectively. Both endpoints were inhibited by ZES treatment alone and were further reduced by the combination of Mf and ZES. Significant convergence of signaling occurs between Mf and locally delivered mTOR inhibitors at S6K. This further impairs endothelial recovery/proliferation via an S6K-dependent mechanism. Patients receiving Mf in combination with stents that elute mTOR inhibitors are potentially at increased risk of delayed endothelial healing and stent thrombosis.

The Effect of a Substrate Containing Arbuscular Mycorrhizal Fungi and Rhizosphere Microorganisms (Trichoderma, Bacillus, Pseudomonas and Streptomyces) and Foliar Fertilization on Growth Response and Rhizosphere pH of Three Strawberry Cultivars

Vegetatively propagated plants of three strawberry cultivars-‘Senga Sengana’, ‘Elsanta’ and ‘Kent’-were grown for 20 weeks in rhizoboxes filled with 1.85 kg of sterilized mineral soil. Ten plants were treated with an N-P-K foliar fertilizer (F, control), or inoculated with a substrate containing arbuscular mycorrhizal fungi, Trichoderma viride and rhizosphere bacteria (PGPR-Plant Growth Promoting Rhizobacteria) without any fertilization (M), or inoculated with the mixture of microorganisms and treated with the foliar fertilizer (MF). Total plant biomass was increased by the M treatment in all cultivars. M treatment resulted in higher total root length and number of root tips in ‘Senga Sengana’, whereas the other two cultivars showed different responses of root morphology. Shoot/root ratio was decreased by the M and MF treatments in comparison with control plants. Foliar fertilization of inoculated plants caused different growth responses in the three cultivars and a general decrease of root growth. After the MF treatment, the biomass of ‘Senga Sengana’ increased and the biomass of ‘Elsanta’ and ‘Kent’ decreased. Inoculation with the mycorrhiza-PGPR substrate increased rhizosphere pH irrespective of foliar fertilization. Plant mineral content was highly modified by the treatments in all the cultivars examined. In particular, changes were noted in N, P, K, Fe, B and Mn uptake. The results show an interaction between foliar fertilization and root inoculation with microorganisms, as well as genotype-dependent influences, on growth responses and rhizosphere pH of strawberry plants.

Production of trans C18:1 and conjugated linoleic acid in continuous culture fermenters fed diets containing fish oil and sunflower oil with decreasing levels of forage

Previously, feeding fish oil (FO) and sunflower seeds to dairy cows resulted in the greatest increases in the concentrations of vaccenic acid (VA, t11 C18:1) and conjugated linoleic acid (CLA) in milk fat. The objective of this study was to evaluate the effects of forage level in diets containing FO and sunflower oil (SFO) on the production of trans C18:1 and CLA by mixed ruminal microbes. A dual-flow continuous culture system consisting of three fermenters was used in a 3 × 3 Latin-square design. Treatments consisted of (1) 75:25 forage:concentrate (HF); (2) 50:50 forage:concentrate (MF); and (3) 25:75 forage:concentrate (LF). FO and SFO were added to each diet at 1 and 2 g/100 g dry matter (DM), respectively. The forage source was alfalfa pellets. During 10-day incubations, fermenters were fed treatment diets three times daily (140 g/day, divided equally between three feedings) as TMR diet. Effluents from the last 3 days of incubation were collected and composited for analysis. The concentration of trans C18:1 (17.20, 26.60, and 36.08 mg/g DM overflow for HF, MF, and LF treatments, respectively) increased while CLA (2.53, 2.35, and 0.81 mg/g DM overflow) decreased in a linear manner (P < 0.05) as dietary forage level decreased. As dietary forage levels decreased, the concentrations of t10 C18:1 (0.0, 10.5, 33.5 mg/g DM) in effluent increased ( P < 0.05) and t10c12 CLA (0.08, 0.12, 0.35 mg/g DM) tended to increases (P < 0.09) linearly. The concentrations of VA (14.7, 13.9, 0.0 mg/g DM) and c9t11 CLA (1.78, 1.52, 0.03 mg/g DM) in effluent decreased in a linear manner ( P < 0.05) as dietary forage levels decreased. Decreasing dietary forage levels resulted in t10 C18:1 and t10c12 CLA replacing VA and c9t11 CLA, respectively, in fermenters fed FO and SFO.

Photoautotrophic Growth and Net Photosynthetic Rate of Sweet Potato Plantlets In Vitro as Affected by the Number of Air Exchanges of the Vessel and Type of Supporting Material

To produce high-quality sweet potato plantlets rapidly at low production costs, single nodal leafy cuttings of sweet potato ( Ipomoea batatas (L.) Lam.) plantlets were cultured in vitro for 14 days on sugar- and phytohormone-free Murashige and Skoog (MS) liquid medium, at a photosynthetic photon flux (PPF) of 200 μmol · m −2 · s −1 and a CO 2 concentration ( v/ v) of 1.8×10 −3. A factorial experiment was conducted with two levels of the number of air exchanges of the vessel (NAE), 8.7-12.2 h −1 and ≥12.2 h −1, and two types of supporting material, vermiculite and Florialite (a porous material). The control treatment consisted of a photomixotrophic culture using a sugar- and NAA-containing agar MS medium with an NAE of 2.4 h −1. PPF and CO 2 concentrations were the same as the photoautotrophic treatments. In comparison with the control treatment, the photoautotrophic treatments with NAE of 8.7–12.2 h −1 (MF treatment) and ≥12.2 h −1 (HF treatment) were, respectively, 2.2 and 2.8 times in dry weight, and 3.7 and 4.2 times in net photosynthetic rate, when Florialite was used. The survival percentages of the plantlets in the field were, respectively, 86% and 97% in the MF and HF treatments, and 35% and 46% higher than that in the control treatment. The plantlets cultured with Florialite showed greater growth, compared with those cultured with vermiculite. Photoautotrophic micropropagation system with high NAE and the use of porous supporting material can produce high-quality plantlets and make it possible to reduce production costs.

Effect of varying carbohydrate and fat content of milk replacer on body composition of Holstein bull calves.

The objective of this study was to determine the effect of varying concentrations of dietary fat and carbohydrate on changes in body composition of Holstein bull calves fed under isocaloric and isonitrogenous intake conditions. Thirty-two calves were assigned to a randomized block design with three dietary treatments, eight calves per treatment, and one baseline group of eight calves. Animals were reared from birth to 85 kg live BW (SEM = 0.57). All calves began treatments between 2 and 6 d of age. Three different milk replacer treatment diets were designed to deliver 14.8 (low fat, LF), 21.6 (medium fat, MF), or 30.6% of DM (high fat, HF) fat; 55.3, 46.7, or 35.4% of DM lactose; and 23.5, 24.8, or 27.0% of DM CP, respectively. Gross energy values were 4.62, 5.09, and 5.77 Mcal/kg for the LF, MF, and HF milk replacers, respectively. From d 1 to 14, calves were offered 0.24 Mcal intake energy/kg BW(0.75), adjusted weekly based on increases in BW, and 0.28 Mcal intake energy/kg BW(0.75) from d 15 to slaughter. Dry feed was not offered. Dry matter, energy, CP, and fat intakes were 55.2 kg, 257.6 Mcal, 13.0 kg, and 8.2 kg; 52.8 kg, 268.8 Mcal, 13.1 kg, and 11.4 kg; and 46.8 kg, 270.3 Mcal, 12.6 kg, and 14.3 kg for the LF, MF and HF treatments, respectively. Energy and CP intakes did not differ among treatments (P = 0.63 and 0.79, respectively). Fat and DMI were different among treatments (P = 0.001 and 0.02, respectively). Empty BW gains were 0.61, 0.61, and 0.65 kg/d for LF, MF, and HF, respectively, and were not different among treatments (P = 0.27). Empty body CP, water, and ash gain were not different among treatments (P = 0.65, 0.99, and 0.57, respectively). Empty body retained energy and fat gain were 27.2 and 57.7% greater for calves fed the HF than for those fed the LF diet (P = 0.06 and 0.006, respectively). Fat as a percentage of the whole empty body on a water-free basis was lower for calves consuming the LF diet (28.6%) than for those fed the HF diet (34.6%), whereas percentage of CP on an empty body, water-free basis was greater for calves consuming the LF diet (59.2%) than for those fed the HF diet (54.9%) (P = 0.006). The results of this study demonstrated that, under isocaloric and isonitrogenous intake conditions, equivalent dietary energy from fat compared to carbohydrate, above 15% fat, has no beneficial purpose unless additional fat deposition is required in the animal. Further, the data demonstrate significant changes in body composition independent of growth rate.

Availability of nitrogen from municipal biosolids for dryland forage grass

A 3-yr study, initiated in 1996, evaluated the availability of N from applied biosolids for dryland forage grass production under the cool, continental climatic conditions in central British Columbia. Treatments included 600 (LB), 1200 (MB) and 1800 (HB) kg total N ha−1 applied as municipal biosolids, a single application of 150 kg N ha−1 as urea in the first year of the experiment (SF), a multiple application of 150, 60 and 30 kg N ha−1 as urea in the first, second, and third years of the experiment (MF), and a control that received no biosolids or urea. All treatments were roto-tilled to 15-cm depth and seeded to a mixture of four grasses. The LB treatment was predicted to supply a similar quantity of plant-available N as the MF treatment, assuming 25, 10, and 5% of biosolids N is available in the first, second, and third year, respectively. Soil N fertility was poor as indicated by the very low forage yield and N uptake in the control, and minimal apparent net soil N mineralisation. Recovery of urea N in the crop over 3 yr averaged only 27%, likely reflecting net immobilisation in this recently broken site and accumulation of N in non-harvested portions of the crop. Cumulative recovery of N from biosolids in the harvested forage averaged only 11%. However, the fertiliser N equivalency of the biosolids N (ratio of recovery of biosolids N to urea N) was estimated at 41%, close to the predicted value of 40%. Forage yield and N uptake were similar for the LB and MF treatments, suggesting that actual biosolids N availability was similar to that predicted. Limited forage yield increase for the HB compared with the MB treatment early in the experiment, and high forage nitrate content for the HB treatment in the first year, suggest that the HB treatment initially supplied an excessive quantity of N. Both urea and biosolids applications increased cumulative uptake of other macro- and micro-nutrients, with forage Cu concentrations reaching values in the establishment year that may be of concern for some animal species. Monitoring of forage NO3 and Cu concentrations is advisable where biosolids are applied. Key words: Phleum pratense L., Dactylis glomerata, Bromus inermis, Bromus biebersteinii, soil N mineralisation, NO3 toxicity

Evaluation of Activator Solutions, Motility Duration, and Short‐Term Storage of Paddlefish Spermatozoa

AbstractMilt from paddlefish (Polyodon sparhula) was collected, examined for motility, and pooled. Six different solutions (dechlorinated tap water, ovarian fluid, bacteriostatic water, distilled water, 0.9% sodium chloride saline water, and milt plasma) were examined for activation and duration of spermatozoal motility. Most solutions except saline solution and milt plasma promoted activation of spermatozoa. Dechlorinated tap water was found to be the best activator with significantly longer duration of spermatozoal motility than the other tested solutions. Saline solution and milt plasma appear to be useful as carrier solutions because of their property of maintaining inactive, viable spermatozoa.Paddlefish milt in three treatments was evaluated for chilled storage [without additives (MF); with 500 IU penicillin and 500 mg streptomycin mix in milt plasma (MP); and 0.9% saline solution (MS)]. The three treatments were stored at 2.4 ± 0.9 C in a precooled, moisture‐saturated oxygen environment and observed every 24 h for 9 d. Motility of activated spermatozoa in MS (7 d) was significantly longer than MF or MP treatments (7 d). Spermatozoa in MS had the longest chilled storage time (8 d).