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Hypoxanthine is the principal inhibitor of murine oocyte maturation in a low molecular weight fraction of porcine follicular fluid.

机译:次黄嘌呤是低分子量级分的猪卵泡液中鼠卵母细胞成熟的主要抑制剂。

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摘要

Studies were carried out to identify and quantify the porcine follicular fluid (PFF) component(s) responsible for inhibition of murine oocyte maturation. A low molecular weight fraction of PFF (less than 1000) was prepared by dialysis and used in all experiments. This PFF fraction contained an inhibitor(s) of mouse oocyte maturation that absorbed maximally in the ultraviolet (UV) range at 250-260 nm. When the PFF fraction was charcoal-extracted, significant loss of absorbance at 250, 260, and 280 nm resulted, which corresponded to loss of inhibitory activity. Four major components of PFF were separated by ion-exchange chromatography and characterized according to their UV spectral characteristics and inhibitory activity. When individual fractions demonstrating identical spectra were pooled and analyzed by high-performance liquid chromatography, the first pooled fraction (A) was found to be impure, but adenine comprised 80% of the UV-absorbing material. Fractions B, C, and D were characterized as pure uracil, hypoxanthine, and 7-methylinosine, respectively. The concentrations of these compounds in PFF were estimated to be 0.06 mM adenine, 0.44 mM uracil, 1.41 mM hypoxanthine, and 0.19 mM 7-methylinosine. Comparison of the potencies of commercial preparations of these compounds established that hypoxanthine is the major inhibitory component of the low molecular weight PFF fraction. Moreover, a commercial preparation of hypoxanthine mimicked the action of PFF on mouse oocyte maturation in that it produced a transient inhibition of oocyte maturation that was significantly potentiated by follicle-stimulating hormone and dibutyryl cyclic adenosine monophosphate. When the inhibitory efficacies of purine and pyrimidine bases and nucleosides were compared, their relative potencies in decreasing order were purine bases greater than purine nucleosides greater than pyrimidine bases = pyrimidine nucleosides. We conclude that hypoxanthine is the predominant low molecular weight component of PFF that inhibits mouse oocyte maturation but that other purines/pyrimidines may also play a role in vivo in maintaining meiotic arrest.
机译:进行研究以鉴定和定量负责抑制鼠卵母细胞成熟的猪卵泡液(PFF)成分。通过透析制备低分子量的PFF(小于1000),并用于所有实验中。该PFF馏分包含一种小鼠卵母细胞成熟抑制剂,该抑制剂在250-260 nm的紫外线(UV)范围内最大吸收。当PFF馏分用木炭萃取时,会导致在250、260和280 nm处的吸光度显着下降,这与抑制活性降低相对应。 PFF的四个主要成分通过离子交换色谱分离,并根据其紫外光谱特征和抑制活性进行表征。合并显示相同光谱的各个馏分并通过高效液相色谱法进行分析时,发现第一个合并的馏分(A)不纯,但腺嘌呤占紫外线吸收材料的80%。馏分B,C和D的特征分别是纯尿嘧啶,次黄嘌呤和7-甲基肌苷。这些化合物在PFF中的浓度估计为0.06 mM腺嘌呤,0.44 mM尿嘧啶,1.41 mM次黄嘌呤和0.19 mM 7-甲基肌苷。比较这些化合物的商业制剂的效能,可以确定次黄嘌呤是低分子量PFF组分的主要抑制成分。此外,次黄嘌呤的商业制剂模仿了PFF对小鼠卵母细胞成熟的作用,因为它产生了对卵母细胞成熟的瞬时抑制作用,该抑制作用可通过刺激卵泡的激素和二丁酰基环式腺苷单磷酸显着增强。当比较嘌呤和嘧啶碱基和核苷的抑制效果时,它们的相对效力递减顺序为:嘌呤碱基大于嘌呤核苷,大于嘌呤核苷大于嘧啶碱基=嘧啶核苷。我们得出的结论是次黄嘌呤是PFF的主要低分子量成分,可抑制小鼠卵母细胞的成熟,但其他嘌呤/嘧啶在体内也可能在维持减数分裂停滞中发挥作用。

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