Suppr超能文献

不同年龄雄性和雌性大鼠中磺基转移酶mRNA表达的调控。

Regulation of sulfotransferase mRNA expression in male and female rats of various ages.

作者信息

Klaassen C D, Liu L, Dunn R T

机构信息

Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City 66160-7417, USA.

出版信息

Chem Biol Interact. 1998 Feb 20;109(1-3):299-313. doi: 10.1016/s0009-2797(97)00141-5.

Abstract

Sulfotransferases (SULTs) are Phase II drug-metabolizing enzymes that catalyze the addition of a sulfuryl moiety to both endogenous compounds, including steroids and neurotransmitters, and certain xenobiotics, including N-hydroxy-2-acetylaminoflourine and phenolic compounds, like alpha-naphthol. In contrast to certain Phase I drug-metabolizing enzymes, little is known about the regulation of the sulfotransferases. These series of studies were designed to analyze SULT mRNA expression and hormonal regulation in male and female rats. The hepatic expression of six different SULT isoforms was examined including three phenol SULTs and three hydroxysteroid SULTs. SULT mRNA expression was examined in adult and developing rats, as well as, in hypophysectomized (HX) and growth hormone-supplemented HX animals. SULT1A1 is thought to be important for the sulfation of simple phenols and its mRNA expression is about twice as high in adult male as in female rats. This difference in SULT1A1 mRNA levels is largely due to a greater decrease in mRNA levels after puberty in female than in male rats. Hypophysectomy resulted in a decrease in expression of SULT1A1 mRNA in both male and female rats. Replacement of growth hormone (GH) by either intermittent injection (male pattern) or infusion (female pattern) failed to restore SULT1A1 expression. Sulfotransferase SULT1C1 has been implicated in activation of N-hydroxyacetylaminoflourine. In contrast to SULT1A1, SULT1C1 mRNA expression is about 10-fold higher in adult males than in adult female rats. This male-dominant expression pattern emerges at 40-50 days of age and is due to an increase in SULT1C1 mRNA in males. Hypophysectomy abolished SULT1C1 expression in male rats. Interestingly, replacement of GH by injection (male pattern) restored SULT1C1 mRNA expression in males and enhanced SULT1C1 expression in female rats to levels observed in adult male rats. GH infusion (female pattern) did not affect SULT1C1 mRNA expression in either male or female rats. Estrogen sulfotransferase (SULT1E2) may play a role in estrogen homeostasis. Adult male rats express SULTIE2 mRNA at levels 10-fold higher than those observed in adult females and similar to SULT1C1, this is due to an increase in SULT1E2 mRNA occurring during puberty in the male rat. Hypophysectomy did not appreciably affect SULT1E2 expression in male rats, however in contrast to males, hypophysectomy markedly enhanced SULT1E2 expression in female rats. GH infusion suppressed SULT1E2 levels in HX male rats. The expression of hydroxysteroid sulfotransferases was also examined. The SULT-20/21 isoform was expressed in both male and female rats. Male expression of this isoform peaked at 30 days of age and then declined to approximately 30% of the level observed in adult females. SULT-20/21 mRNA expression increased sharply at 45 days of age in female rats and remained elevated. Expression of SULT-20/21 mRNA was decreased markedly by hypophysectomy in both male and female rats. GH injection did not affect SULT-20/21 mRNA expression in HX males, however this treatment resulted in a 4-fold increase in SULT-20/21 mRNA in HX females. GH infusion restored SULT-20/21 expression in HX-male rats. GH infusion did elevate SULT-20/21 mRNA expression in female-HX rats, but not to the level observed in intact females. Hydroxysteroid SULT isoform SULT-40/41 was expressed in adult female but not adult male rats. SULT-40/41 expression peaked at 15 days of age in both male and female rats and decreased thereafter. The decrease in expression was more pronounced in male rats. SULT-60 mRNA, like SULT-40/41, was expressed only in adult female rats. Male rats express SULT-60 at 30 days of age, but SULT-60 mRNA is undetectable at 60 days. SULT-60 mRNA was expressed in females only after day 30 and female SULT-60 mRNA expression remains high thereafter. SULT-40/41 and SULT-60 mRNA expression was increased by HX in male rats and decreased by HX in female rats. (ABSTRACT TRUNCATED)

摘要

磺基转移酶(SULTs)是Ⅱ相药物代谢酶,可催化将一个磺酰基部分添加到内源性化合物(包括类固醇和神经递质)以及某些外源性物质(包括N-羟基-2-乙酰氨基芴和酚类化合物,如α-萘酚)上。与某些Ⅰ相药物代谢酶不同,关于磺基转移酶的调节知之甚少。这一系列研究旨在分析雄性和雌性大鼠中SULT mRNA的表达及激素调节情况。检测了六种不同SULT同工型的肝脏表达,包括三种酚类SULT和三种羟基类固醇SULT。在成年和发育中的大鼠中,以及在垂体切除(HX)和补充生长激素的HX动物中检测了SULT mRNA的表达。SULT1A1被认为对简单酚类的硫酸化很重要,其mRNA表达在成年雄性大鼠中约为雌性大鼠的两倍。SULT1A1 mRNA水平的这种差异主要是由于雌性大鼠青春期后mRNA水平的下降幅度大于雄性大鼠。垂体切除导致雄性和雌性大鼠中SULT1A1 mRNA的表达均下降。通过间歇性注射(雄性模式)或输注(雌性模式)补充生长激素均未能恢复SULT1A1的表达。磺基转移酶SULT1C1与N-羟基乙酰氨基芴的活化有关。与SULT1A1相反,SULT1C1 mRNA表达在成年雄性大鼠中比成年雌性大鼠高约10倍。这种雄性主导的表达模式在40-50日龄时出现,是由于雄性大鼠中SULT1C1 mRNA增加所致。垂体切除消除了雄性大鼠中SULT1C1的表达。有趣的是,通过注射(雄性模式)补充生长激素可恢复雄性大鼠中SULT1C1 mRNA的表达,并将雌性大鼠中SULT1C1的表达提高到成年雄性大鼠中观察到的水平。生长激素输注(雌性模式)对雄性或雌性大鼠中SULT1C1 mRNA的表达均无影响。雌激素磺基转移酶(SULT1E2)可能在雌激素稳态中起作用。成年雄性大鼠中SULTIE2 mRNA的表达水平比成年雌性大鼠高10倍,与SULT1C1类似,这是由于雄性大鼠青春期期间SULT1E2 mRNA增加所致。垂体切除对雄性大鼠中SULT1E2的表达没有明显影响,然而与雄性不同,垂体切除显著增强了雌性大鼠中SULT1E2的表达。生长激素输注抑制了HX雄性大鼠中SULT1E2的水平。还检测了羟基类固醇磺基转移酶的表达。SULT-20/21同工型在雄性和雌性大鼠中均有表达。该同工型在雄性大鼠中的表达在30日龄时达到峰值,然后下降至成年雌性大鼠中观察到水平的约30%。雌性大鼠中SULT-20/21 mRNA表达在45日龄时急剧增加并保持升高。垂体切除在雄性和雌性大鼠中均显著降低了SULT-20/21 mRNA的表达。生长激素注射对HX雄性大鼠中SULT-20/21 mRNA的表达没有影响,然而这种处理导致HX雌性大鼠中SULT-20/21 mRNA增加了4倍。生长激素输注恢复了HX雄性大鼠中SULT-20/21的表达。生长激素输注确实提高了HX雌性大鼠中SULT-20/21 mRNA的表达,但未达到完整雌性大鼠中观察到的水平。羟基类固醇SULT同工型SULT-40/41在成年雌性大鼠中表达,但在成年雄性大鼠中不表达。SULT-40/41的表达在雄性和雌性大鼠中均在15日龄时达到峰值,此后下降。雄性大鼠中表达的下降更为明显。SULT-60 mRNA与SULT-40/41一样,仅在成年雌性大鼠中表达。雄性大鼠在30日龄时表达SULT-60,但在60日龄时无法检测到SULT-60 mRNA。SULT-60 mRNA仅在30日龄后在雌性中表达,此后雌性SULT-60 mRNA表达保持高水平。垂体切除增加了雄性大鼠中SULT-40/41和SULT-60 mRNA的表达,降低了雌性大鼠中SULT-40/41和SULT-60 mRNA的表达。(摘要截断)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验