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      • Open Access Article

        1 - Isolation and Morphological Characterization of Ovine Adipose-Derived Mesenchymal Stem Cells in Scanning Electron Microscopy (SEM)
        M. Mohebbi G. Moghaddam B. Qasemi Panahi M. Nouri
        The main purpose of this study is to provide advanced insights into scanning electron microscopy (SEM) of adipose derived mesenchymal stem cells (oAD-MSCs). In this study after isolation and proliferation of AD-MSCs, their cell surface markers characterized using antibo More
        The main purpose of this study is to provide advanced insights into scanning electron microscopy (SEM) of adipose derived mesenchymal stem cells (oAD-MSCs). In this study after isolation and proliferation of AD-MSCs, their cell surface markers characterized using antibodies RT-PCR. SEM was used to study of ultrastructure of oAD-MSCs. Adipose tissue was obtained from tail fat of sheep. Surface markers (CD44, CD90, CD34, CD31) evaluated by RT-PCR. RT-PCR was done for CD44, CD90, CD34 and CD31 to identify of cells. Morphological characterization was done by inverted microscope and SEM. Cells was prepared by glutaraldehyde for first fixation and tetroxide osmium for second fixation and dehydration with different percent of ethanol. Finally, cells coated with gold and observed in SEM. Adipose derived mesenchymal stem cells (AD-MSCs) were isolated and proliferated. They were positive for CD44 and CD90 markers and negative for CD31 and Cd34 markers in RT-PCR technique. AD-MSCs showed a fibroblast-like, spindle-shaped morphology after they attached to the culture flasks observing in inverted microscope. Explanted specimens were imaged with scanning electron microscopy (SEM). SEM provides the main technology to visualize surface features. In SEM the outer surface of the mesenchymal cells could be observed; so, in this study, the pseudopods arising from each cell and extending through each other were clearly shown. Manuscript profile
      • Open Access Article

        2 - Photoperiod as a Factor for Studying Fluctuations ofSeminal Traits during Breeding and Non-BreedingSeason
        M.M. Pourseif G.H. Moghaddam S.A. Rafat H. Daghighkia A. Pourseif
        The main purpose of this study was to evaluate the influence of the photoperiod on the seminal traits of crossbreed wool-producing rams throughout on year period. For the effect of photoperiod two periods were considered: decreasing daylight length (summer and autumn) a More
        The main purpose of this study was to evaluate the influence of the photoperiod on the seminal traits of crossbreed wool-producing rams throughout on year period. For the effect of photoperiod two periods were considered: decreasing daylight length (summer and autumn) and increasing daylight length (winter and spring). For the study 5 Baluchi × Moghani (BL×MG) and 5 Arkharmerino × Moghani (AM×MG) rams were used. Semen collection started from first of October 2010 to end of September 2011. After a training period of 2 weeks semen ejaculates were evaluated for volume, total sperm count per ejaculate (TSE), spermatozoa concentration, semen color, wave motion, percentage of progressive motility, percentage of live and abnormal spermatozoa, semen pH, methylene blue reduction time (MBRT) and semen index (semen volume × spermatozoa concentration/mL × live spermatozoa % × progressive motility %).Analysis of the yearlong data showed that semen samples with the best quality were collected in September to November (P<0.05). Significant seasonal variations of semen traitswere observed for all of seminal traitsexcept for progressive motility, percentage of live spermatozoa and MBRT. Yet, nostatistical differences were found between the two genetic groups (P>0.05). Although there were significant seasonal changes in semen characteristics of the crosses, the fresh semen showed adequate quality to be used for artificial or natural insemination all around the year. Photoperiod was found to influence semen production in two genetic groups at 38 ˚02' N, 46 ˚27' E at an altitude of 1567 m above sea level of Iran. However, these effects should are not detrimental to the use of rams for breeding purposes throughout the year. Manuscript profile
      • Open Access Article

        3 - Cryopreservation of Spermatogonial Stem Cells of Native Goat of Iran
        M. Mohebbi G. Moghaddam B. Qasemi-Panahi H. Daghigh Kia S.A. Rafat G. Hamidian
        This study deals with cryopreservation of spermatogonial stem cells (SSCs) of native goat using different media along with cryoprotectant. Morphological differentiation and immunocytochemistry tests were used to identify the cells. Furthermore anti-vimentin and anti-Oct More
        This study deals with cryopreservation of spermatogonial stem cells (SSCs) of native goat using different media along with cryoprotectant. Morphological differentiation and immunocytochemistry tests were used to identify the cells. Furthermore anti-vimentin and anti-Oct-4 immuno staining methods were used for identification of sertoli cells and SSCs, respectively. Cryopreservation of SSCs was done with two sets of media. One with 40% dulbecco’s modified eagle’s medium (DMEM), 50% fetal bovine serum (FBS) and 10% dimethyl sulfoxide (DMSO). The second medium included 90% FBS and 10% DMSO. Post thaw cryopreserved cells were subjected to viability and colony area formation on 4th, 8th and 12th days of culturing after and before cryopreservation. Results clearly indicated the viability, area and number of colonies in the first medium registered to 61.37%, 0.87 mm2and 246.88 averagely in every 25 cm2 culture flask, respectively. Similarly with second medium, post thaw cryopreserved sperm registered viability, area and number of colonies to 73.87%, 2.74 mm2 and 364.36 in every 25 cm2 culture flask, respectively. After the thawing of spermatogonial cells, the best viability percentage was obtained in the freezing medium containing 90% FBS. Thus the study demonstrated that serum concentration had a distinct positive effect on the maintenance and proliferation of SSCs in culture after cryopreservation. Manuscript profile
      • Open Access Article

        4 - Study of Reproductive Performance of Crossbred Ewes Treated with GnRH and PMSG during Breeding Season
        G.H. Moghaddam A. Olfati H. Daghigh Kia S.A. Rafat
        Reproductive performance was evaluated in non-lactating crossbred ewes to which were administered the exogenous GnRH and PMSG. The ewes were randomly allocated in three treatment groups (n=40).After accurate detection of estrus and 2 hours prior to mating, 2.5 mL of dis More
        Reproductive performance was evaluated in non-lactating crossbred ewes to which were administered the exogenous GnRH and PMSG. The ewes were randomly allocated in three treatment groups (n=40).After accurate detection of estrus and 2 hours prior to mating, 2.5 mL of distilled water and 2.5 mL of GnRH were injected intramuscular to each ewe of the first (control) and second group, respectively. In the third group, the ewes were pretreated with CIDR for 14 days and received 400 IU PMSGat the time of withdrawal of the CIDR. After injection of PMSG, fixed-time artificial insemination was performed with 0.5 mL of fresh diluted semen. No significant differences were observed in term of the pregnancy, lambing, and fecundity rates between ewes treated with GnRH and control group (87.5, 97.5, and 1.114% vs. 75, 82.5, and 1.1%, respectively). Twining rate was higher in the ewes treated with GnRH than synchrony or control groups (18.18, 4, and 6.5%respectively, P<0.05). In the artificially inseminated group, pregnancy, lambing and fecundity rates were 77.5, 62.5, and 0.81%, respectively. In conclusion, the results showed that treatment of ewes with GnRH at time of estrus and prior to mating, improved the conception and twining birth rates. Also injection of PMSG after CIDR removal caused an increase in efficiency of fertility rate and shorter breeding period. Manuscript profile
      • Open Access Article

        5 - The Effect of Prepubertal Castration on Wool Diameter and Blood Testosterone in Ghezel Breed
        ف. نظری-زنوز ق. مقدم س.ع. رافت ز. عبدی ک. اعتماد گرگان ر. نبوی
        Wool growth depends on hormones activity. Owing to hormonal status is extensively affected by surgical excision of endocrine glands, disease or severe congenital abnormalities, wool growth will be altered. This study intends to assess the effect of prepubertal castratio More
        Wool growth depends on hormones activity. Owing to hormonal status is extensively affected by surgical excision of endocrine glands, disease or severe congenital abnormalities, wool growth will be altered. This study intends to assess the effect of prepubertal castration at different ages on wool traits and testosterone with draw in male lambs. One month of age Ghezel male lambs (n=20) were selected and allotted in 5 groups (n=4 lambs per group), 4 groups (1, 2, 3, 4 month ages) were surgically castrated, while the fifth group served as control. All animal were fed with the same ration for 240 days. At 9-month of age, hair samples were taken from the mid-side and shoulder regions and analyzed by image analysis. Blood samples were taken from all animals from 1 month of age to 9 month monthly to measure plasma levels of testosterone. The average fiber diameter in castrated lambs was lower compared with intact males (35.21 µm vs. 36.40 µm; P<0.05). Also, 4-month castrated lambs showed significant differences in the average diameter of wool fiber in comparison to the other castrated groups (P<0.05). The plasma level of testosterone in castrated lambs remained in basal levels (0.51 ng/mL), contrasting to values recorded in intact male lambs at 9-month of age (2.33 ng/mL; P<0.05). The diameter of fibers was strongly correlated (P<0.05) with testosterone plasma concentration (r=0.94) in castrated and in intact lambs (r=0.86). Therefore, it is concluded that testosterone concentration affects the diameter of wool. Manuscript profile
      • Open Access Article

        6 - The Effect of Apricot Tree Gum on the Quality of Frozen and Melted Ram Sperm in the Breeding Season
        P. Khanzadeh G. Maghaddam H. Daghighkia S.A. Rafat R. Moradi
        The adding gum of some fruit trees preserves the quality of semen during the freezing and thawing process. The aim of this study was to investigate the antioxidant effects as well as the sugars in apricot tree gum to increase the quality of ram semen during the freezing More
        The adding gum of some fruit trees preserves the quality of semen during the freezing and thawing process. The aim of this study was to investigate the antioxidant effects as well as the sugars in apricot tree gum to increase the quality of ram semen during the freezing, storage and thawing process. In this study, 4 treatments were used. The control group was without any apricot and the three treated groups were pure and sterilized apricot gum with concentrations of 10, 15 and 20 mg/mL in a tris-based diluent. Semen collection was performed twice a week during the breeding season using artificial vagina, and sampling was replicated 5 times for each ram. After transferring the samples to the laboratory and diluting them to ensure that they meet the required standards. After cooling the straws in the refrigerator, they were placed in liquid nitrogen. Total motility, progressive motion, survival, abnormality and membrane integrity assessment were measured in the first, 15th, 30th, 45th and 60th days after freezing. Plasma malondialdehyde levels were also assessed after thawing on day 60. The three treated groups of 10, 15 and 20 mg/mL in diluent were significantly different from the control group in total motility, progressive motion, survival, abnormality, membrane integrity, and malondialdehyde levels (P<0.05). There was no significant difference among the treatments of 10, 15 and 20 mg/mL in diluent in all measured traits (P>0.05). However, the treatment of 20 mg/mL had the highest total motility, membrane viability and integrity, and the lowest malignancy and malondialdehyde, and groups of 10 and 15 mg/mL had the highest progressive motion (P<0.05). Considering the results, use of apricot tree gum can improve the quality of sperm cryopreservation. Manuscript profile