Evaluating the Impact of Minimized GnRH and PGF Analogues-Loaded Chitosan Nanoparticles on Ovarian Activity and Fertility of Heat-Stressed Dairy Cows.

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmaceutics Pub Date : 2025-02-18 DOI:10.3390/pharmaceutics17020274
Mohammed E A Omar, Eman M Hassanein, Ahmed M Shehabeldin, Ottó Szenci, Abdelghany A El-Shereif
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Abstract

Objectives: This study aimed to evaluate the effectiveness of gonadotropin-releasing hormone-loaded chitosan-TPP nanoparticles (GnRH-CNPs) and prostaglandin F-loaded chitosan-TPP nanoparticles (PGF-CNPs) within the Ovsynch protocol for enhancing reproductive performance in heat-stressed dairy cows. Methods: Thirty-six cyclic purebred Friesian cows not detected in standing heat for more than 90 days postpartum were randomly allocated to three treatment groups. The control group (OVS, n = 12) followed the standard Ovsynch protocol with conventional doses. The ½ OVS group (n = 12) received 5 µg GnRH-CNPs on days 0 and 9, along with 250 µg PGF-CNPs on day 7. While the ¼ OVS group (n = 12) was administered 2.5 µg GnRH-CNPs on days 0 and 9, with 125 µg PGF-CNPs on day 7. Ovarian follicular dynamics and corpus luteum (CL) development were monitored on days 0, 4, 7, and 9 of the protocol. Serum progesterone (P4) concentrations were measured throughout the synchronization period and on days 15 and 30 post-AI. Pregnancy was diagnosed on day 30 post-AI. Results: The ¼ OVS protocol achieved a significantly greater follicular response (p < 0.05) than other protocols. On day 4, following the first GnRH administration, the OVS group exhibited a higher number of subordinate follicles (p < 0.05) and a greater diameter of the dominant follicles (DFs), whereas the ¼ OVS group showed a greater subordinate follicle diameter (p < 0.05) and a higher number of DFs. On day 9, after PGF administration, the ¼ OVS group maintained an elevated number of subordinate follicles, while larger subordinate follicle diameters were observed in the ½ OVS and OVS groups. No significant differences in DF numbers and diameters were observed among groups. P4 concentrations remained similar across groups during treatments. Compared to control, a significantly higher value of P4 concentration (p < 0.05) was recorded on day 15 post-AI in the ½ OVS group and on day 30 post-AI in the ¼ OVS group. These findings correlated with a higher pregnancy rate in the ¼ OVS group (65%) compared to the ½ OVS and OVS groups (40% in each). Conclusions: Nanofabrication reduced GnRH and PGF dosage by 50% and 75% without impairing ovarian response and pregnancy rates. The ¼ OVS protocol notably enhanced the ovarian activity and fertility, highlighting the use of GnRH-CNPs and PGF-CNPs as promising and practical approaches to enhance the fertility in dairy cattle under heat stress (HS).

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评价最小化GnRH和PGF2α类似物负载壳聚糖纳米颗粒对热应激奶牛卵巢活性和生育能力的影响。
目的:本研究旨在评价促性腺激素释放激素负载壳聚糖- tpp纳米颗粒(GnRH-CNPs)和前列腺素f2 α负载壳聚糖- tpp纳米颗粒(PGF2α-CNPs)在ovsync方案下提高热应激奶牛繁殖性能的效果。方法:选取36头产后90 d以上无立热的循环纯种弗里西亚奶牛,随机分为3个治疗组。对照组(OVS, n = 12)采用常规剂量的标准ovsync方案。½OVS组(n = 12)在第0天和第9天给予5µg GnRH-CNPs,第7天给予250µg PGF2α-CNPs。而¼OVS组(n = 12)在第0天和第9天给予2.5µg GnRH-CNPs,第7天给予125µg PGF2α-CNPs。在方案的第0,4,7和9天监测卵巢卵泡动力学和黄体(CL)的发育。在整个同步期以及ai后第15天和第30天测定血清孕酮(P4)浓度。人工智能后第30天诊断怀孕。结果:¼OVS方案的卵泡反应显著高于其他方案(p < 0.05)。第1次GnRH给药后第4天,OVS组下属卵泡数量增多(p < 0.05),优势卵泡(DFs)直径增大,而¼OVS组下属卵泡直径增大(p < 0.05), DFs数量增多。第9天,给药后,¼OVS组下属卵泡数量增加,而½OVS组和OVS组下属卵泡直径增大。各组间DF数和直径无显著差异。治疗期间各组P4浓度保持相似。与对照组相比,½OVS组ai后第15天和¼OVS组ai后第30天P4浓度显著升高(p < 0.05)。这些发现与¼OVS组的怀孕率(65%)比½OVS组和OVS组(各40%)高相关。结论:纳米制造可使GnRH和PGF2α剂量分别降低50%和75%,而不影响卵巢反应和妊娠率。OVS方案显著提高了奶牛卵巢活性和生育能力,突出了GnRH-CNPs和PGF2α-CNPs是提高奶牛热应激(HS)生育能力的有前途和实用的方法。
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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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