{"title":"Niosomal nanocarriers loaded with artemisinin has potential to enhance the functional characteristics of cryo-preserved equine spermatozoa","authors":"Azam Abbasi , Houshang Nouri , Firooz Samadi","doi":"10.1016/j.anireprosci.2024.107653","DOIUrl":null,"url":null,"abstract":"<div><div>Cryopreservation is a crucial method for the preservation of genetic materials. Nevertheless, this technique can have adverse effects due to cryo-oxidative damage. The primary objective of this study was to investigate the cryo-protective effects of niosomal nanocarriers loaded with artemisinin (NN-Art) on the functional attributes of equine spermatozoa. The parameters examined included sperm motility and kinematics through computer-assisted sperm analysis (CASA), plasma membrane integrity via the hypoosmotic swelling test, viability using the eosin-nigrosin staining technique, morphology with Hancock's solution, and lipid peroxidation through the thiobarbituric acid reactive substances assay. Additionally, flow cytometry was applied to assess mitochondrial membrane potential, reactive oxygen species (ROS) levels, sperm chromatin structure, and apoptotic-like changes. The CASA indicated a greater enhancement in the total and progressive motility and as well straight line velocity following the addition of NN-Art into the cryo-diluent medium compared with the conventional form of artemisinin and control (P < 0.05). Moreover, the incorporation of cryo-diluent medium with NN-Art demonstrated a greater efficiency in the improvement of viability, proportion of spermatozoa abnormality, plasma membrane functionality, and lipid peroxidation (P < 0.05). The flow cytometry assessment demonstrated a significant enhancement in mitochondrial potential activity, a reduction in the level of ROS, and an increase in the proportion of live spermatozoa along with a decrease in late apoptotic stallion post-thawed spermatozoa treated with both Art and specifically NN-Art. The results of this study suggest that NN-Art exhibit enhanced antioxidant capabilities, which are crucial for improving the functional quality of equine spermatozoa by mitigating cryo-oxidative stress.</div></div>","PeriodicalId":7880,"journal":{"name":"Animal Reproduction Science","volume":"272 ","pages":"Article 107653"},"PeriodicalIF":2.2000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Animal Reproduction Science","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378432024002537","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Cryopreservation is a crucial method for the preservation of genetic materials. Nevertheless, this technique can have adverse effects due to cryo-oxidative damage. The primary objective of this study was to investigate the cryo-protective effects of niosomal nanocarriers loaded with artemisinin (NN-Art) on the functional attributes of equine spermatozoa. The parameters examined included sperm motility and kinematics through computer-assisted sperm analysis (CASA), plasma membrane integrity via the hypoosmotic swelling test, viability using the eosin-nigrosin staining technique, morphology with Hancock's solution, and lipid peroxidation through the thiobarbituric acid reactive substances assay. Additionally, flow cytometry was applied to assess mitochondrial membrane potential, reactive oxygen species (ROS) levels, sperm chromatin structure, and apoptotic-like changes. The CASA indicated a greater enhancement in the total and progressive motility and as well straight line velocity following the addition of NN-Art into the cryo-diluent medium compared with the conventional form of artemisinin and control (P < 0.05). Moreover, the incorporation of cryo-diluent medium with NN-Art demonstrated a greater efficiency in the improvement of viability, proportion of spermatozoa abnormality, plasma membrane functionality, and lipid peroxidation (P < 0.05). The flow cytometry assessment demonstrated a significant enhancement in mitochondrial potential activity, a reduction in the level of ROS, and an increase in the proportion of live spermatozoa along with a decrease in late apoptotic stallion post-thawed spermatozoa treated with both Art and specifically NN-Art. The results of this study suggest that NN-Art exhibit enhanced antioxidant capabilities, which are crucial for improving the functional quality of equine spermatozoa by mitigating cryo-oxidative stress.
期刊介绍:
Animal Reproduction Science publishes results from studies relating to reproduction and fertility in animals. This includes both fundamental research and applied studies, including management practices that increase our understanding of the biology and manipulation of reproduction. Manuscripts should go into depth in the mechanisms involved in the research reported, rather than a give a mere description of findings. The focus is on animals that are useful to humans including food- and fibre-producing; companion/recreational; captive; and endangered species including zoo animals, but excluding laboratory animals unless the results of the study provide new information that impacts the basic understanding of the biology or manipulation of reproduction.
The journal''s scope includes the study of reproductive physiology and endocrinology, reproductive cycles, natural and artificial control of reproduction, preservation and use of gametes and embryos, pregnancy and parturition, infertility and sterility, diagnostic and therapeutic techniques.
The Editorial Board of Animal Reproduction Science has decided not to publish papers in which there is an exclusive examination of the in vitro development of oocytes and embryos; however, there will be consideration of papers that include in vitro studies where the source of the oocytes and/or development of the embryos beyond the blastocyst stage is part of the experimental design.