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  1. NTU Theses and Dissertations Repository
  2. 生物資源暨農學院
  3. 動物科學技術學系
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/55392
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dc.contributor.advisor吳兩新(Leang-Shin Wu),邱智賢(Chih-Hsien Chiu)
dc.contributor.authorJyun-Yuan Wangen
dc.contributor.author王俊淵zh_TW
dc.date.accessioned2021-06-16T04:00:03Z-
dc.date.available2018-02-03
dc.date.copyright2015-02-03
dc.date.issued2014
dc.date.submitted2014-11-13
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/55392-
dc.description.abstract動物透過內分泌系統以調控許多生理機制,睪丸內的萊吉氏細胞(Leydig cells)、卵巢內的粒性細胞(granulosa cell)、黃體細胞(luteal cell)以及腎上腺皮質細胞(adrenal cortical cell)透過類固醇生成(steroidogenesis)合成許多類固醇內泌素以調控生理功能。這些細胞主要受到內泌素分子調控其功能,然而處理特定蛋白質、藥物或是來自植物中的植化素(phytochemicals)亦可以調控類固醇生成細胞,因此本研究的目的在探討特定情況下類固醇生成會如何受到調控。
雄性素為前列腺癌細胞生長所必需,因此抑制體內雄性素濃度為治療前列腺癌的第一要務。文獻指出薑黃所萃取的薑黃素(curcumin)具有抑制腫瘤細胞生長並促進凋亡的功效,本研究則發現薑黃素亦有抑制萊吉氏細胞合成睪固酮的功效。此現象與細胞內促進Star表現的轉錄因子之mRNA表現量受到薑黃素抑制有關,證實了薑黃素可抑制睪固酮合成,因此在治療前列腺癌更有優勢。
代謝症候群(metabolic syndrome)已成為廣受討論的健康議題並且與代謝性症狀包括高血壓、高血脂以及糖尿病息息相關。糖尿病在男性糖尿病患者中造成的併發症包括勃起障礙(erectile dysfunction, ED),其成因除了神經與心血管性之外,亦有研究認為高血糖會對睪丸產生氧化壓力(oxidative stress)而使其所合成的睪固酮濃度低下而使得血管內皮細胞無法合成足夠的一氧化氮(nitric oxide)以維持血管舒張以及勃起反應。本研究以模擬糖尿病的動物模式,證實高血糖或胰島素阻抗的情況下,確實會透過增加睪丸內氧化壓力,並抑制類固醇生成基因表現以及睪固酮合成,給予槲黃素(quercetin)處理可以有效改善因胰島素阻抗所造成的睪固酮濃度低下;肥胖亦為代謝症候群中常見的症狀之一,肥胖時體內上升的瘦體素(leptin)已被證實能抑制腎上腺對ACTH刺激的反應而抑制其醣類皮質素的分泌。在高脂飼糧誘發肥胖小鼠模式中,我們證實了體內瘦體素濃度較高的小鼠對於ACTH的反應較差,處理槲黃素後則可改善。根據相關文獻我們推論,槲黃素可以影響瘦體素下游訊息傳遞路徑,並增加腎上腺細胞內cAMP濃度,以維持其類固醇生成功能,然確切的證據仍需細胞學的研究加以證實。
類固醇內泌素中多數為性內泌素,因此類固醇生成的調控在生殖生理中至為重要。有文獻指出懷孕母畜攝食松葉會造成流產,肇因於松葉中的異柏油酸(isocupressic acid)具有抑制孕酮分泌的功能。小鼠萊吉氏細胞株MA-10的研究成果顯示,處理異柏油酸會抑制蛋白激酶A的磷酸化,並抑制Star與Cyp11a1的表現最後抑制類固醇生成。最後,近年來對於kisspeptin在生殖生理方面的研究都集中在其對於腦部的功能,本研究的最後一部分則探討其是否具有直接調控睪丸類固醇生成的功能。結果發現kisspeptin並不會直接調控初代萊吉氏細胞的睪固酮分泌能力,但後續實驗則暗示了kisspeptin可能參與調控睪丸的發育過程。
綜上所述,除了現今已知的內泌素分子之外,植化素亦有調控類固醇生成的能力。這些研究的成果提供了新藥開發可參考的未來方向可透過影響類固醇內泌素的合成以調控正常生理。
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dc.description.abstractAnimals use endocrine system to regulate physiological mechanisms. Leydig cell, granulosa cell, luteum cell and adrenal cortical cell producing steroid hormones controlled by endrocrine system through steroidogenesis. However, specific peptides, chemicals and phytochemicals extract from plants are found can regulate steroidogenesis. The purpose of this study is to clearify the mechanism of how steroidogenesis be effected under specific condition.
Androgen is necessary for prostate cancer growth so decreasing androgen level is important in prostate cancer treatment. Curcumin was found inhibiting proliferation and metastasis of prostate cancer cell lines. Here we found that curcumin inhibits testosterone production in Leydig cell via suppressing expression of sterodiogenic genes. These results provide more evidences on curcumin as an effective drug for the treatment of prostate cancer.
Metabolic syndrome is closely links to many symptoms including hypertension, hypercholesterolemia and diabetes. Erectile dysfunction is one symptoms of diabetes. With diabetic mice models, we comfirmed that hyperglycemia induced oxidative stress decrease testosterone level through suppressing steroidogenic genes expressionn in testis. Support quercetin as antioxidant restores testosterone production under insulin resistance. The other hand, leptin elevated in obese individual suppresses adrenal response to ACTH stimulation also glucocorticoid secretion. In this study, we confirm high leptin level in high-fat diet-induced obese mice cause poor adrenal response to ACTH while quercetin restores adrenal response. We hypothesize that quercetin interfere JAK2-PI3K pathway to restore adrenal steroidogenesis suppressed by leptin, more evidences are need to prove this hypothesis.
Consumption of ponderosa pine needles causes late-term abortions in cattle and isocupressic acid (IA) responsible for the effect. With murine Leydig cell MA-10, we found that IA does not affect enzyme activities of steroidogenic genes but inhibits their expression through attenuating cAMP-PKA signaling. Thus, steroid production was suppressed. Since testes are essential for male reproduction and recent studies show that Kiss1 and Kiss1r are expressed in testes. To investigate their function in testes, primary mice Leydig cell was used in this study. Our results showed that Kiss1 did not affect testosterone production in primary Leydig cells, but suggest that expression pattern of KISS1 follows the stages of testicular development. Future studies are need to determine if kisspeptin regulates testicular development during puberty.
In general, steroidogenesis is important to physiological regulation, this report demonstrate that some phytochemicals can effect steroids production directly, these results provide new direction on new food additives development and new drog discovery.
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Previous issue date: 2014
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dc.description.tableofcontents摘要 1
Abstract 3
第1章 緒言 6
1.1 類固醇內泌素 6
1.2 類固醇分泌細胞膜上受體之交互作用 8
1.3 類固醇生成(steroidogenesis)之分子機制 14
1.4 植化素(phytochemicals) 16
第2章 薑黃素抑制類固醇生成之分子機制探討 (The Molecular Mechanism of Inhibitory Effect by Curcumin on Steroidogenesis) 19
第一節 前言 19
2.1.1 前列腺癌與去勢抗性前列腺癌(castration-resistant prostate cancer, CRPC) 19
2.1.2 類固醇生成路徑與非傳統路徑(backdoor pathway) 20
2.1.3 Abiraterone Acetate 21
2.1.4 薑黃素(curcumin)與其對前列腺癌效果之相關研究 22
2.1.5 薑黃素對類固醇生成之影響 23
第二節 材料與方法 25
2.2.1 試劑與藥品 25
2.2.2 初代小鼠萊吉氏細胞培養 25
2.2.3 薑黃素處理對C57BL/6小鼠初代萊吉氏細胞睪固酮分泌能力之影響 26
2.2.4 細胞培養 26
2.2.5 SRB assay 27
2.2.6 MTT assay 27
2.2.7 孕酮、皮質醇、皮質固酮與睪固酮之測定 28
2.2.8 細胞內鈣離子染色 28
2.2.9 RNA萃取與cDNA合成 29
2.2.10 即時聚合酶連鎖反應(real-time PCR) 29
2.2.11 蛋白質萃取與定量 29
2.2.12 西方點墨法 30
第三節 結果 31
2.3.1 薑黃素對初代培養萊吉氏細胞類固醇生成的影響 31
2.3.2 薑黃素對MA-10細胞類固醇生成的影響 32
2.3.3 薑黃素對腎上腺細胞類固醇生成的影響 32
2.3.4 薑黃素處理對MA-10細胞內鈣離子濃度變化之影響 33
2.3.5 薑黃素對類固醇生成相關基因表現量之影響 34
2.3.6 薑黃素處理對轉錄因子mRNA表現量之影響 35
第四節 討論 36
第五節 結論 41
第3章 代謝症候群中高血糖對類固醇生成的影響 (Effect of Leptin and Hyperglycemia on Steroidogenesis)) 54
第一節 前言 54
3.1.1 代謝症候群(metabolic syndrome, Mts) 54
3.1.2 糖尿病 55
3.1.3 胰島素的生理功能 56
3.1.4 胰島素阻抗(insulin resistance) 59
3.1.5 胰島素阻抗與慢性發炎 61
3.1.6 STZ誘發第一型糖尿病動物模式 62
3.1.7 糖尿病與勃起障礙 62
3.1.8 高血糖對類固醇生成的影響 63
3.1.9 植化素的抗氧化效果與其作為治療高血糖透過氧化壓力抑制類固醇生成藥物之潛力 66
第二節 材料與方法 68
3.2.1 試劑與藥品 68
3.2.2 血漿萃取類固醇 68
3.2.3酵素免疫分析法(enzyme immunoassay, EIA) 69
3.2.4 STZ誘發第一型糖尿病小鼠 69
3.2.6 小鼠萊吉氏細胞初代培養 71
3.2.7 口服葡萄糖耐受性試驗(oral glucose tolerance test, OGTT) 71
3.2.8 胰島素耐受性試驗(insulin resistance test, IRT) 72
3.2.9 血液生化值分析 72
3.2.10 RNA萃取與cDNA合成 73
3.2.11 即時聚合酶連鎖反應(real-time PCR) 73
3.2.13 小鼠睪丸丙二醛(malondialdehyde, MDA)測定 74
3.2.15 胰島素測定與HOMA計算 75
3.2.16 數據整理 75
第三節 結果 77
3.3.1 STZ誘導第一型糖尿病小鼠之體重、血糖與血液生化值變化 77
3.3.2 STZ處理對小鼠性腺與睪固酮分泌能力之影響 77
3.3.3 槲黃素處理對胰島素阻抗之效果 79
3.3.4 第一型糖尿病模式小鼠睪丸中睪固酮合成所需基因之表現差異 79
3.3.5 氧化壓力下睪丸中內質網壓力相關基因與Hmox1表現 80
第四節 討論 81
第五節 結論 90
第4章 槲黃素回復瘦體素抑制腎上腺類固醇生成之效用評估 (Evaluation of Recoverable Ability of Qucetin on Leptin Suppressed Adrenal Steroidogenesis) 106
第一節 前言 106
4.1.1 腎上腺解剖構造與腎上腺皮質生理功能 106
4.1.2 下視丘-腦垂線-腎上腺軸(hypothalamic pituitary adrenal axis, HPA axis) 107
4.1.3 腎上腺皮質類固醇生成的分子機制 108
4.1.4 醣類皮質素在能量代謝中扮演的角色 110
4.1.5 肥胖與瘦體素(leptin) 113
4.1.6 瘦體素對腎上腺功能之影響 115
4.1.7 槲黃素(quercetin) 116
第二節 材料與方法 119
4.2.1 試劑與藥品 119
4.2.2 酵素免疫分析法 119
4.2.3 活體試驗 120
4.2.4 ACTH challenge測試 120
4.2.5 口服葡萄糖耐受性試驗 121
4.2.6 血漿中瘦體素含量分析 121
4.2.7 血漿中胰島素含量分析 122
4.2.8 細胞株培養及類固醇產物分析 122
4.2.9 數據整理 123
第三節 結果 124
4.3.1 高脂飼糧與槲黃素處理對C57BL/6小鼠體重、血糖,採食量與飲水量之變化 124
4.3.2 高脂飼糧與槲黃素處理對C57BL/6小鼠腎上腺對ACTH反應及血漿瘦體素含量之影響 124
4.3.3 高脂飼糧與槲黃素處理對C57BL/6小鼠血漿胰島素與homeostatic modem assssment (HOMA)之影響 125
4.3.4 高脂飼糧與槲黃素處理對C57BL/6小鼠肝比重與脂肪分佈之影響 125
4.3.5 高脂飼糧與槲黃素處理對C57BL/6小鼠血液生化值之影響 126
4.3.6 瘦體素對H295細胞皮質醇分泌能力之影響 126
第四節 討論 127
第五節 結論 132
第5章 異柏油酸抑制MA-10細胞類固醇生成之分子機制探討 (Molecular Mechanism of Isocupressic Acid Suppress MA-10 Cell Steroidogenesis) 146
第一節 前言 146
第二節 材料與方法 148
5.2.1 試劑與藥品 148
5.2.2 初代小鼠萊狄氏細胞培養 148
5.2.3 MA-10細胞培養 149
5.2.4 MTT assay 149
5.2.5 孕酮及睪固酮之測定 150
5.2.6 RNA萃取與cDNA合成 150
5.2.7 即時聚合酶連鎖反應 151
5.2.8 西方點墨法 151
5.2.9 數據整理 152
第三節 結果 153
5.3.1 IA對初代培養小鼠萊狄氏細胞睪固酮合成能力之影響 153
5.3.2 IA對MA-10細胞孕酮合成能力與細胞活性之影響 153
5.3.3 IA對由22R-OHC或孕烯醇酮增進的MA-10孕酮分泌之影響 154
5.3.4 IA對MA-10細胞類固醇生成相關基因的表現量影響 154
5.3.4 IA對MA-10細胞類固醇生成相關基因之蛋白質表現量影響 155
第四節 討論 156
第五節 結論 160
第6章 小鼠萊吉氏細胞中Kisspeptin表現與年齡之關係 (Kisspeptin Expression in Mouse Leydig Cells Correlates with Age)) 171
第一節 前言 171
第二節 材料與方法 173
6.2.1 試劑與藥品 173
6.2.2 動物實驗 173
6.2.3 初代小鼠萊吉氏細胞培養 174
6.2.4酵素免疫分析法測定睪固酮 174
6.2.5 RNA萃取,cDNA合成及即時聚合酶連鎖反應 175
6.2.6 免疫組織化學染色 176
6.2.7數據分析 177
第三節 結果 178
6.3.1 Kisspeptin與peptide 234對初代萊吉氏細胞由ovine LH促進之睪固酮合成能力之影響 178
6.3.2 Kisspeptin與peptide 234對初代萊吉氏細胞22-hydroxycholesterol或孕烯醇酮促進之睪固酮合成能力之影響 178
6.3.3 小鼠發育時睪丸成長以及血漿中睪固酮的變化 179
6.3.4 小鼠發育時睪丸內Lhcgr, Star, Cyp11a1, 與 Hsd3b1 mRNA 表現量差異 179
6.3.5小鼠發育時睪丸內Kiss1, Kiss1r 與 Esr1 mRNA 表現量差異 179
第四節 討論 181
第五節 結論 185
參考文獻 194
附錄 234
實驗溶液配方 234
著作發表: 241
dc.language.isozh-TW
dc.subject類固醇生成zh_TW
dc.subject植化素zh_TW
dc.subject睪固酮zh_TW
dc.subject醣類皮質素zh_TW
dc.subject代謝症候群zh_TW
dc.subjectPhytochemicalsen
dc.subjectTestosteroneen
dc.subjectGlucocorticoidsen
dc.subjectSteroidogenesisen
dc.subjectMetabolic Syndromeen
dc.title植化素調節類固醇生成機制之探討zh_TW
dc.titleStudy of Regulation of Steroidogenesis by Phytochemicalsen
dc.typeThesis
dc.date.schoolyear103-1
dc.description.degree博士
dc.contributor.oralexamcommittee鍾德憲(De-Shien Jong),陳億乘(Yi-Chen Chen),梁耀仁(Yao-Jen Liang)
dc.subject.keyword類固醇生成,植化素,睪固酮,醣類皮質素,代謝症候群,zh_TW
dc.subject.keywordSteroidogenesis,Phytochemicals,Testosterone,Glucocorticoids,Metabolic Syndrome,en
dc.relation.page241
dc.rights.note有償授權
dc.date.accepted2014-11-14
dc.contributor.author-college生物資源暨農學院zh_TW
dc.contributor.author-dept動物科學技術學研究所zh_TW
顯示於系所單位:動物科學技術學系

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