Mevalonate pathway and thecal-interstitial function
Mevalonate pathway and thecal-interstitial function
批准号:
7883163
负责人:
Antoni J Duleba
金额:
$31.34万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-05-22 至 2012-06-30
关键词:
AddressAffectAndrogensAntioxidantsCell Culture TechniquesCholesterolClinicalClinical TrialsDevelopmentFunctional disorderGrowthHumanHyperplasiaLightLuteinizing HormoneMesenchymeMonomeric GTP-Binding ProteinsOvarianOxidative StressPathway interactionsPhosphorylationPlayPolycystic Ovary SyndromeProductionRattusResearchRoleSignal Transduction PathwaySimvastatinSteroid biosynthesisTestingTestosteroneTissuesVascular Smooth MuscleWomanbasedesigninsightinterstitialinterstitial cellisoprenylationmevalonatenovelnovel therapeutic interventionresearch studyrho
中文摘要
描述(由申请人提供):适当的卵巢发育和功能需要调节膜间质细胞的生长和类固醇生成的机制。在病理条件下,如多囊卵巢综合征(PCOS),膜间质间质增生,产生过量的雄激素。这一建议旨在验证甲氧戊酸途径在调节卵巢膜间质细胞的生长和功能中发挥重要作用这一新的假设。我们推测甲氧丙酮酸途径通过:(I)改变Ras和Rho等小GTP酶的异戊二烯基化从而影响调节生长的信号转导途径,(Ii)调节类固醇合成底物的可用性,以及(Iii)改变氧化应激水平,进而影响生长和类固醇合成,从而影响膜-间质细胞。最终,我们认为,他汀类药物抑制甲戊酸途径可能纠正PCOS的主要特征,包括膜间质细胞过度生长、雄激素过度产生和氧化应激。这一假说是建立在证据的基础上的,在一些组织中,如血管平滑肌,甲戊酸途径的产物促进了小GTP酶的异戊二烯基化,从而激活了促进生长的信号转导途径。在血管平滑肌和其他几种组织中,他汀类药物抑制甲氧戊酸途径会抑制生长,发挥抗氧化作用,并减少胆固醇的合成。我们的初步研究表明,适度的氧化应激增加,他汀类药物抑制膜间质细胞的增殖和类固醇合成,同时抑制ERK1/2的磷酸化。我们还完成了一项试点临床试验,我们发现辛伐他汀可以降低多囊卵巢综合征患者的睾酮和黄体生成素水平。这项建议的具体目的是深入研究甲戊酸途径在膜-间质细胞中的作用:(I)生长,(Ii)类固醇合成和(Iii)氧化应激。这些目标将通过对大鼠和人膜间质细胞培养的实验来实现。这些研究结果将为甲羟戊酸途径在卵巢间充质生长和功能中的作用提供新的认识。最终,这项拟议的研究可能会为PCOS的病理生理学提供新的线索,并为开发新的治疗方法提供动力,例如他汀类药物的临床应用。
英文摘要
DESCRIPTION (provided by applicant): Appropriate ovarian development and function require mechanisms regulating growth and steroidogenesis of theca-interstitial cells. Under pathological conditions such as polycystic ovary syndrome (PCOS), theca-interstitial compartment is hyperplastic and produces excessive amounts of androgens. This proposal is designed to test the novel hypothesis that the mevalonate pathway plays an important role in modulation of growth and function of the ovarian theca-interstitial cells. We postulate that mevalonate pathway affects theca-interstitial cells by: (i) altering isoprenylation of small GTPases such as Ras and Rho affecting thus signal transduction pathways regulating growth, (ii) modulating the availability of substrates for steroidogenesis, and (iii) altering the level of oxidative stress, which, in turn, affects growth and steroidogenesis. Ultimately, we propose that, inhibition of the mevalonate pathway by agents such as statins may correct major features of PCOS including excessive growth of theca-interstitial cells, excessive androgen production and oxidative stress. This hypothesis is based on evidence that in several tissues, such as vascular smooth muscle, products of the mevalonate pathway facilitate isoprenylation of small GTPases and thus activate signal transduction pathways promoting growth. In vascular smooth muscle and in several other tissues, inhibition of the mevalonate pathway by statins inhibits growth, exerts antioxidant effects and decreases cholesterol synthesis. Our preliminary studies have shown that moderate oxidative stress increases and statins inhibit proliferation and steroidogenesis of theca-interstitial cells while blocking ERK1/2 phosphorylation. We have also completed a pilot clinical trial and we found that simvastatin decreases testosterone and luteinizing hormone in women with PCOS. The specific aims of this proposal are to study in depth the role of the mevalonate pathway in theca-interstitial cells on: (i) growth, (ii) steroidogenesis and (iii) oxidative stress. These aims will be addressed by experiments on rat and human theca-interstitial cell cultures. The results of these studies will provide a new insight into the role of mevalonate pathway on the growth and function of ovarian mesenchyme. Ultimately, the proposed research may shed new light on the pathophysiology of PCOS and provide an impetus towards the development of new therapeutic approaches, such as clinical use of statins.
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会议论文
Mevalonate pathway and thecal-interstitial function
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批准号:7260120
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项目类别:
-
资助金额:$0.0万
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财政年份:2007
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负责人:Antoni J Duleba
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依托单位:
Mevalonate pathway and thecal-interstitial function
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批准号:8099791
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项目类别:
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资助金额:$30.08万
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财政年份:2007
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负责人:Antoni J Duleba
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依托单位:
Effects of Statins on Endometrial Stoma
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批准号:7318135
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项目类别:
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资助金额:$28.26万
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财政年份:2007
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负责人:Antoni J Duleba
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依托单位:
Mevalonate pathway and thecal-interstitial function
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批准号:7501132
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项目类别:
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资助金额:$31.68万
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财政年份:2007
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负责人:Antoni J Duleba
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依托单位:
Mevalonate pathway and thecal-interstitial function
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批准号:7638018
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项目类别:
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资助金额:$31.65万
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财政年份:2007
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负责人:Antoni J Duleba
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依托单位:
Mevalonate pathway and thecal-interstitial function
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批准号:7429638
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项目类别:
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资助金额:$31.65万
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财政年份:2007
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负责人:Antoni J Duleba
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依托单位:
Role of Antioxidants in Ovarian Thecal Hyperplasiar
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批准号:6862633
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项目类别:
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资助金额:$29.43万
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财政年份:2002
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负责人:Antoni J Duleba
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依托单位:
Role of Antioxidants in Ovarian Thecal Hyperplasiar
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批准号:6430576
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项目类别:
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资助金额:$22.07万
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财政年份:2002
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负责人:Antoni J Duleba
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依托单位:
Role of Antioxidants in Ovarian Thecal Hyperplasiar
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批准号:6701749
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项目类别:
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资助金额:$29.43万
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财政年份:2002
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负责人:Antoni J Duleba
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依托单位:
Role of Antioxidants in Ovarian Thecal Hyperplasiar
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批准号:6621113
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项目类别:
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资助金额:$29.43万
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财政年份:2002
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负责人:Antoni J Duleba
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依托单位:
Effects of Statins on Endometrial Stoma
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批准号:8065989
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项目类别:
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资助金额:$33.52万
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财政年份:--
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负责人:Antoni J Duleba
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依托单位:
Effects of Statins on Endometrial Stoma
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批准号:8256515
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项目类别:
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资助金额:$31.75万
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财政年份:--
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负责人:Antoni J Duleba
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依托单位:
Effects of Statins on Endometrial Stoma
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批准号:7656586
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项目类别:
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资助金额:$31.79万
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财政年份:--
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负责人:Antoni J Duleba
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依托单位:
Effects of Statins on Endometrial Stoma
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批准号:7880010
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项目类别:
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资助金额:$34.68万
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财政年份:--
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负责人:Antoni J Duleba
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依托单位:
海外基金