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Study Of Fetal Sex Determination Based On External Genitalia And Gonadal Differentiation In Water Buffalos

机译:基于外生殖器和性腺分化的水牛确定胎儿性别的研究

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This study was performed on 102 embryos and fetuses that were collected from Ahvaz slaughter house. The specimens was divided in three group, on the basis of external genitalia differentiation and crown Rump Length (CRL), as groups 1,2 and 3. The embryos of group 1 (No. 63, CRL-10-83cm) showed completely developed external genitalia of male and female, so there was no doubts in the recognition of their sexes. The embryos of group 2 (No. 19, CRL-4-10cm) also showed clear sex on the basis of genital tubercle (clitoris in the female and penis in the male embryos) and genital swellings (lips of vulva in the females and scrotum in the males). The tip of genial tubercle of females embryos have showed dorso-caudally and of males ventro-cranially directions, respectively. In the embryos of group 3 (No. 20, CRL=0.38-4 cm). The determination of sex was not possible by help of external genitalia. So, the gonads of these embryos, were removed from abdominal cavity and after histological preparations, stained by H & E and PAS methods. On the basis of histological studies, the sex differentiation of gonads to testis and ovary were recognized in embryos with CRL=2.1 cm, and CRLl<2.3 cm respectively. The gonads of embryos with CRL<2.1 cm were recognized as undifferentiated. These findings indicated that the sex differentiation starts earlier in the gonads compare to external genitalia but the differentiation of gonad and external genitalia of male has priority to female embryos.The sex of embryos were not recognized in undifferentiated gonad neither by external genitalia nor histological structure. Introduction Mammalian sex determination proceeds in three distinct phases. In the first stage, genetic sex is determined at the time of fertilization by the chromosomal complement of the fertilizing spermatozoon. Later, during embryonic development , this genetic information is translated in to gonadal sex that determines the growth of either a testis or ovary from a bipotential early indifferent gonad.The third stage which is the phenotypic sex determination, begins in fetal or early post-natal life and continues through puberty, a period in which endocrine products of the gonads direct the differentiation of the accessory sex ducts and external genitalia (Loffler and Koopman, 2003). External and gonadal sex differentiation has been studied in human and domestic animals with different results.In male human fetus, at 7th week of fetal life, under the influence of Y chromosome, primary sex cords containing proliferated coelomic epithelium and primordial germ cells continue their proliferation and form medullary (testicular) cords. Synchronously a thick fibrous layer called tunica albuginea forms due to proliferation of mesenchyme. The female gonads differentiate later than male. Because of the absence of Y chromosome, the primary sex cords degenerate and coelomic epithelium proliferates and form cortical or secondary sex cords that are characteristic of early female gonad (Sadler, 2004).Sex differentiation has been studied in human (Baker and Scrimgeour, 1980), swine (Inomata et al., 1993), dog (Evans, 1979), bovine (Erickson, 1966), horse (Sakai, 1955) and goat (Harshan et al., 1994 and banankhojasteh et al., 2006). However, only few studies on ovarian differentiation in water buffalo fetuses was reported (Ghannam and Deeb,1969).In many parts of the world, water buffaloes (bubalus bubalis) are raised for production of milk, meat, hide and down. Water buffaloes have high adaptability and can live in different climates. During recent decades, universal concentration on water buffaloes has in creased especially in Asian countries and new initiatives have been starting for development of related industries. Therefore, conduction of basic and applied research regarding various aspects of water buffaloes seems necessary.Because there is no comprehensive study on external and gonadal sex differentiation in fetus and in view of the fact that studies on va
机译:这项研究是对从阿瓦士屠宰场收集的102个胚胎和胎儿进行的。根据外生殖器分化和冠臀长(CRL)将标本分为三组,分别为1,2组和3组。第1组(第63号,CRL-10-83cm)的胚胎显示出完全发育男性和女性的外生殖器,因此在性别识别方面毫无疑问。第2组的胚胎(第19号,CRL-4-10cm)在生殖器结节(雌性中的生殖器和雄性胚中的阴茎)和生殖器肿胀(雌性和阴囊的外阴唇)的基础上也表现出清晰的性别。在男性中)。雌性胚的总和结节的尖端分别显示了背尾尾方向和雄性腹影方向。在第3组的胚胎中(第20号,CRL = 0.38-4cm)。借助于外生殖器无法确定性别。因此,将这些胚胎的性腺从腹腔中取出,并在进行组织学准备后,用H&E和PAS方法进行染色。根据组织学研究,在CRL = 2.1 cm和CRL1 <2.3 cm的胚胎中分别识别出性腺向睾丸和卵巢的性别分化。 CRL <2.1 cm的胚胎的性腺被认为是未分化的。这些发现表明,与外部生殖器相比,性腺的性别分化开始得更早,但男性的性腺和外部生殖器的分化优先于女性的胚胎。未分化的性腺中的性别没有被外部生殖器和组织学结构所识别。简介哺乳动物的性别决定分为三个不同的阶段。在第一阶段,受精时的基因性别由受精精子的染色体互补决定。后来,在胚胎发育过程中,这种遗传信息被转化为性腺性行为,该性行为决定了双电位早期性腺无性生殖中睾丸或卵巢的生长。第三阶段是表型性别确定,始于胎儿或出生后早期。生命并持续到青春期,在这个时期,性腺的内分泌产物指导性交管道和外生殖器的分化(Loffler and Koopman,2003)。研究了人类和家畜的外部和性腺性别分化,结果却不同。在男性胎儿中,在胎儿生命的第7周,在Y染色体的影响下,含有增殖的结肠上皮和原始生殖细胞的原性索继续增殖并形成髓(睾丸)索。同步地,由于间充质的增殖,形成了称为白膜的厚纤维层。雌性腺比雄性分化晚。由于缺乏Y染色体,初级性索退化并导致上皮细胞增生并形成皮质或次级性索,这是早期雌性腺的特征(Sadler,2004)。人的性别分化研究(Baker and Scrimgeour,1980) ),猪(Inomata等,1993),狗(Evans,1979),牛(Erickson,1966),马(Sakai,1955)和山羊(Harshan等,1994和banankhojasteh等,2006)。然而,关于水牛胎儿卵巢分化的研究很少(Ghannam and Deeb,1969)。在世界许多地方,水牛(bubalus bubalis)用于生产牛奶,肉,生皮和羽绒。水牛适应性强,可以生活在不同的气候中。在最近的几十年中,对水牛的普遍集中度有所增加,尤其是在亚洲国家,针对相关产业发展的新举措已经开始。因此,有必要对水牛的各个方面进行基础研究和应用研究。因为没有对胎儿的外在和性腺性别分化进行全面研究,而且鉴于对va的研究

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