کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8427476 | 1546059 | 2018 | 16 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Characteristics and fertility of domestic cat epididymal spermatozoa cryopreserved with two different freezing media
ترجمه فارسی عنوان
خصوصیات و باروری اسپرمهای اپیدیدیم گربه خانگی با دو نوع انجماد مختلف
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کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
علوم کشاورزی و بیولوژیک
علوم دامی و جانورشناسی
چکیده انگلیسی
The study represents a comparison of cryopreservation of domestic cat epididymal spermatozoa with two commercially available freezing media: CaniPlus Freeze (CPF) and SpermFreeze (SF). The viability of nonfrozen spermatozoa evaluated by the VitalScreen test was 68.7â¯Â±â¯3.0%. These figures were lower for the frozen-thawed spermatozoa: 51.2â¯Â±â¯6.3% for CPF group and 54.4â¯Â±â¯3.1% for SF group. The motility of nonfrozen spermatozoa was 57.2â¯Â±â¯4.5%. These figures were reduced in both frozen-thawed groups; however, there was no significant difference in these parameters between CPF (30.8â¯Â±â¯7.1%) and SF (27.4â¯Â±â¯8.1%) groups. The percentage of nonprogressively moving motile spermatozoa after freezing-thawing was decreased in both frozen-thawed groups (23.5â¯Â±â¯5.9 and 12.0â¯Â±â¯2.4 for CPF and SF frozen correspondingly) as compared with nonfrozen controls (42.1â¯Â±â¯4.1%). Morphology of spermatozoa was assessed by light microscopy. The mean percentages of normal spermatozoa were 28.5â¯Â±â¯4.1% for nonfrozen group, 26.0â¯Â±â¯2.3% for CPF frozen group, and 23.9â¯Â±â¯1.9% for SF frozen group. The most frequent anomalies in all the three groups were flagella and combined defects. In vitro fertilization (IVF) of domestic cat oocytes with nonfrozen and frozen-thawed spermatozoa produced developing embryos. The percentage of in-vitro-derived embryos was 43.6% after using nonfrozen spermatozoa. Frozen-thawed spermatozoa developed at a similar rate (44.0%) after using SF. However, the rate of embryo development was lower (20.1%) when CPF was used. The in-vitro-derived embryos in the nonfrozen group consisted of 46.9â¯Â±â¯2.5â¯cells after 5-day culturing. After cryopreservation with SF and CPF the cell numbers per embryo were 39.9â¯Â±â¯2.7 and 31.8â¯Â±â¯3.4 correspondingly. In CPF group these numbers were lower than in nonfrozen controls. Cryopreservation of spermatozoa with either of two freezing media led to a decrease in post-thaw viability and motility of spermatozoa but did not affect the rate or spectrum of their morphological anomalies. The use of CPF, but not SF led to a decrease of sperm fertilizing abilities.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Theriogenology - Volume 110, 1 April 2018, Pages 148-152
Journal: Theriogenology - Volume 110, 1 April 2018, Pages 148-152
نویسندگان
Eugeny Brusentsev, Elena Kizilova, Valentina Mokrousova, Valeria Kozhevnikova, Irina Rozhkova, Sergei Amstislavsky,