Modulation of vascular reactivity by selective estrogen receptor modulators and dihydropyridines in porcine coronary arteries.
Leung Hok Sum. === Thesis (M.Phil.)--Chinese University of Hong Kong, 2005. === Includes bibliographical references (leaves 128-147). === Abstracts in English and Chinese. === Declaration --- p.i === Acknowledgements --- p.ii === Abbreviation --- p.iii === Abstract in English --- p.iv === Abstra...
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Online Access: | http://library.cuhk.edu.hk/record=b5892728 http://repository.lib.cuhk.edu.hk/en/item/cuhk-325237 |
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Coronary circulation Selective estrogen receptor modulators Dihydropyridine Coronary Circulation--drug effects Selective Estrogen Receptor Modulators--therapeutic use Selective Estrogen Receptor Modulators--metabolism Dihydropyridines |
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Coronary circulation Selective estrogen receptor modulators Dihydropyridine Coronary Circulation--drug effects Selective Estrogen Receptor Modulators--therapeutic use Selective Estrogen Receptor Modulators--metabolism Dihydropyridines Modulation of vascular reactivity by selective estrogen receptor modulators and dihydropyridines in porcine coronary arteries. |
description |
Leung Hok Sum. === Thesis (M.Phil.)--Chinese University of Hong Kong, 2005. === Includes bibliographical references (leaves 128-147). === Abstracts in English and Chinese. === Declaration --- p.i === Acknowledgements --- p.ii === Abbreviation --- p.iii === Abstract in English --- p.iv === Abstract in Chinese --- p.vi === Contents --- p.viii === Chapter Chapter I - --- Introduction === Chapter 1.1. --- Steroid Hormone --- p.1 === Chapter 1.2. --- Estrogen Receptors --- p.2 === Chapter 1.3. --- Selective Estrogen Receptor Modulators --- p.5 === Chapter 1.3.1. --- Tamoxifen --- p.5 === Chapter 1.3.1.1. --- Cardiovascular Effects of Tamoxifen --- p.6 === Chapter 1.3.1.2. --- Acute Vascular Effects of Tamoxifen --- p.6 === Chapter 1.3.1.3. --- Chronic Vascular Effects of Tamoxifen --- p.7 === Chapter 1.3.1.4. --- Antioxidant Effects of Tamoxifen --- p.8 === Chapter 1.3.2. --- Raloxifene --- p.8 === Chapter 1.3.2.1. --- Cardiovascular Effects of Raloxifene --- p.8 === Chapter 1.3.2.2. --- Acute Vascular Effects of Raloxifene --- p.9 === Chapter 1.3.2.3. --- Chronic Vascular Effects of Raloxifene --- p.10 === Chapter 1.3.2.4. --- Ovariectomy and Raloxifene Treatment --- p.11 === Chapter 1.4. --- Mechanism of Action of SERMs --- p.15 === Chapter 1.5. --- Effects of Functional Endothelium and Nitric Oxide --- p.18 === Chapter 1.6. --- Dihydropyridine (DHP) Calcium Channel Antagonists --- p.19 === Chapter 1.6.1. --- Development of Newer Generation of Dihydropyridines --- p.19 === Chapter 1.6.2. --- Effects of Dihydropyridines on Vascular Endothelium (I) --- p.20 === Chapter 1.6.3. --- Effects of Dihydropyridines on Vascular Endothelium (II) --- p.21 === Chapter 1.6.4. --- Effects of Dihydropyridines on Nitric Oxide Synthase (NOS) --- p.21 === Chapter 1.6.5. --- Clinical Studies of Dihydropyridines --- p.22 === Chapter 1.7. --- Vascular Ion Channels --- p.25 === Chapter 1.8. --- Objectives of The Present Study --- p.26 === Chapter Chapter II - --- Materials and Methods === Chapter 2.1. --- Tissue Preparation --- p.27 === Chapter 2.1.1. --- Preparation of The Porcine Left Circumflex Coronary Arteries --- p.27 === Chapter 2.1.2. --- Removal of Functional Endothelium --- p.27 === Chapter 2.1.3. --- Organ Bath Setup --- p.27 === Chapter 2.1.4. --- Isometric Force Measurement --- p.29 === Chapter 2.2. --- In situ Endothelial [Ca2+]i Imaging --- p.29 === Chapter 2.2.1. --- Preparation of Porcine Left Circumflex Coronary Arteries --- p.29 === Chapter 2.2.2. --- Setup For In situ Endothelial [Ca2+]i Imaging --- p.30 === Chapter 2.3. --- Electrophysiological Measurement of BKCa Current --- p.31 === Chapter 2.3.1. --- Enzymatic Dissociation of Coronary Artery Smooth Muscle Cells --- p.31 === Chapter 2.3.2. --- Electrophysiological Measurement --- p.31 === Chapter 2.4. --- DPPH Free Radical Scavenging Assay --- p.31 === Chapter 2.5. --- Solutions and Drugs --- p.32 === Chapter 2.5.1. --- "Drugs, Chemicals and Enzymes" --- p.32 === Chapter 2.5.2. --- Solutions Used in Force Measurement --- p.34 === Chapter 2.6. --- Statistical Analysis --- p.34 === Chapter Chapter III - --- Tamoxifen-Induced Endothelial Nitric Oxide-Dependent Relaxation in Porcine Coronary Arteries via Ouabain- and BaCl2-Sensitive Mechanisms === Chapter 3.1. --- Abstract --- p.35 === Chapter 3.2. --- Introduction --- p.36 === Chapter 3.3. --- Methods and Materials --- p.37 === Chapter 3.3.1. --- Vessel Preparation --- p.37 === Chapter 3.3.2. --- Isometric Force Measurement --- p.38 === Chapter 3.3.3. --- In situ Endothelial [Ca2+]i Imaging --- p.39 === Chapter 3.3.4. --- Chemicals --- p.40 === Chapter 3.3.5. --- Data Analysis --- p.40 === Chapter 3.4. --- Results --- p.41 === Chapter 3.4.1. --- Relaxant Responses --- p.41 === Chapter 3.4.2. --- Effects of Inhibitors of NO-Dependent Relaxation --- p.41 === Chapter 3.4.3. --- Effects of Putative K+ Channel Blockers and Ouabain --- p.41 === Chapter 3.4.4. --- "Effects of Ouabain, Removal of Extracellular K+ Ions and BaCI2" --- p.42 === Chapter 3.4.5. --- SNP-Induced Relaxation --- p.42 === Chapter 3.4.6. --- Effects of Actinomycin D and Cycloheximide --- p.42 === Chapter 3.4.7. --- Relaxant Effect of 17β-Estradiol --- p.43 === Chapter 3.4.8. --- Effects on Endothelial [Ca2+]i in Isolated Coronary Arteries With Endothelium --- p.43 === Chapter 3.5. --- Discussion --- p.53 === Chapter Chapter IV - --- Endothelium-Independent Relaxation to Raloxifene in Porcine Coronary Arteries === Chapter 4.1. --- Abstract --- p.57 === Chapter 4.2. --- Introduction --- p.58 === Chapter 4.3. --- Methods and Materials --- p.59 === Chapter 4.3.1. --- Vessel Preparation --- p.59 === Chapter 4.3.2. --- Isometric Force Measurement --- p.60 === Chapter 4.3.3. --- Electrophysiological Measurement of BKCa Current --- p.61 === Chapter 4.3.3.1. --- Enzymatic Dissociation of Coronary Artery Smooth Muscle --- p.61 === Chapter 4.3.3.2. --- Electrophysiological Measurement --- p.62 === Chapter 4.3.4. --- Chemicals --- p.63 === Chapter 4.3.5. --- Data Analysis --- p.63 === Chapter 4.4. --- Results --- p.64 === Chapter 4.4.1. --- Effect of Raloxifene on Agonist-Induced Contractions --- p.64 === Chapter 4.4.2. --- Role of Endothelium --- p.64 === Chapter 4.4.3. --- Effect of ER Antagonist --- p.65 === Chapter 4.4.4. --- Effect of Putative K+ Channel Blockers --- p.65 === Chapter 4.4.5. --- Effect of Elevated Extracellular K+ Concentrations --- p.65 === Chapter 4.4.6. --- Effects of Raloxifene on BKCa Current --- p.65 === Chapter 4.5. --- Discussion --- p.75 === Chapter Chapter V - --- Therapeutic Concentrations of Raloxifene Augment Bradykinin Mediated Nitric Oxide-Dependent Relaxation in Porcine Coronary Arteries === Chapter 5.1. --- Abstract --- p.78 === Chapter 5.2. --- Introduction --- p.79 === Chapter 5.3. --- Methods and Materials --- p.80 === Chapter 5.3.1. --- Vessel Preparation --- p.80 === Chapter 5.3.2. --- Isometric Force Measurement --- p.80 === Chapter 5.3.3. --- In situ Endothelial [Ca2+]i Imaging --- p.81 === Chapter 5.3.4. --- Free Radical Scavenging Assay --- p.82 === Chapter 5.3.5. --- Chemicals --- p.83 === Chapter 5.3.6. --- Data Analysis --- p.83 === Chapter 5.4. --- Results --- p.84 === Chapter 5.4.1. --- Relaxation to Bradykinin --- p.84 === Chapter 5.4.2. --- Effect of Raloxifene on Bradykinin-Induced Relaxation --- p.84 === Chapter 5.4.3. --- Effect of Raloxifene on Relaxation Induced by Substance P and --- p.85 === Chapter 5.4.4. --- Effect of Estrogen on Bradykinin-Induced Relaxation --- p.85 === Chapter 5.4.5. --- Effect of Raloxifene on Sodium Nitroprusside-Induced Relaxation --- p.86 === Chapter 5.4.6. --- Free Radical Scavenging Effect --- p.86 === Chapter 5.4.7. --- Raloxifene Augmentation of Bradykinin-Stimulated Endothelial [Ca2+]i --- p.86 === Chapter 5.5. --- Discussion --- p.99 === Chapter Chapter VI - --- "Cilnidipine, a Slow-Acting Ca2+ Channel Blocker, Induces Relaxation in Porcine Coronary Arteries: Role of Endothelial Nitric Oxide and [Ca2+]i" === Chapter 6.1. --- Abstract --- p.102 === Chapter 6.2. --- Introduction --- p.103 === Chapter 6.3. --- Methods and Materials --- p.104 === Chapter 6.3.1. --- Vessel Preparation --- p.104 === Chapter 6.3.2. --- Isometric Force Measurement --- p.105 === Chapter 6.3.3. --- In situ Endothelial [Ca2+]i Imaging --- p.106 === Chapter 6.3.4. --- Free Radical Scavenging Assay --- p.107 === Chapter 6.3.5. --- Chemicals --- p.108 === Chapter 6.3.6 --- Data Analysis --- p.108 === Chapter 6.4. --- Results --- p.108 === Chapter 6.4.1. --- Relaxant Responses --- p.108 === Chapter 6.4.2. --- Role of the Endothelium --- p.109 === Chapter 6.4.3. --- Effect of Inhibitors of NO-Dependent Relaxation --- p.109 === Chapter 6.4.4. --- Effect of Indomethacin and w-conotoxin --- p.110 === Chapter 6.4.5. --- Effect of Cilnidipine on Sodium Nitroprusside-Induced Relaxation --- p.110 === Chapter 6.4.6. --- Effects on Endothelial [Ca2+]i in Isolated Endothelium-Intact Coronary Arteries --- p.110 === Chapter 6.4.7. --- Free Radical Scavenging Effect --- p.110 === Chapter 6.5. --- Discussion --- p.120 === Chapter Chapter VII - --- General Summary --- p.123 === References --- p.128 |
author2 |
Leung, Hok Sum. |
author_facet |
Leung, Hok Sum. |
title |
Modulation of vascular reactivity by selective estrogen receptor modulators and dihydropyridines in porcine coronary arteries. |
title_short |
Modulation of vascular reactivity by selective estrogen receptor modulators and dihydropyridines in porcine coronary arteries. |
title_full |
Modulation of vascular reactivity by selective estrogen receptor modulators and dihydropyridines in porcine coronary arteries. |
title_fullStr |
Modulation of vascular reactivity by selective estrogen receptor modulators and dihydropyridines in porcine coronary arteries. |
title_full_unstemmed |
Modulation of vascular reactivity by selective estrogen receptor modulators and dihydropyridines in porcine coronary arteries. |
title_sort |
modulation of vascular reactivity by selective estrogen receptor modulators and dihydropyridines in porcine coronary arteries. |
publishDate |
2005 |
url |
http://library.cuhk.edu.hk/record=b5892728 http://repository.lib.cuhk.edu.hk/en/item/cuhk-325237 |
_version_ |
1718990269550952448 |
spelling |
ndltd-cuhk.edu.hk-oai-cuhk-dr-cuhk_3252372019-03-05T03:34:23Z Modulation of vascular reactivity by selective estrogen receptor modulators and dihydropyridines in porcine coronary arteries. Coronary circulation Selective estrogen receptor modulators Dihydropyridine Coronary Circulation--drug effects Selective Estrogen Receptor Modulators--therapeutic use Selective Estrogen Receptor Modulators--metabolism Dihydropyridines Leung Hok Sum. Thesis (M.Phil.)--Chinese University of Hong Kong, 2005. Includes bibliographical references (leaves 128-147). Abstracts in English and Chinese. Declaration --- p.i Acknowledgements --- p.ii Abbreviation --- p.iii Abstract in English --- p.iv Abstract in Chinese --- p.vi Contents --- p.viii Chapter Chapter I - --- Introduction Chapter 1.1. --- Steroid Hormone --- p.1 Chapter 1.2. --- Estrogen Receptors --- p.2 Chapter 1.3. --- Selective Estrogen Receptor Modulators --- p.5 Chapter 1.3.1. --- Tamoxifen --- p.5 Chapter 1.3.1.1. --- Cardiovascular Effects of Tamoxifen --- p.6 Chapter 1.3.1.2. --- Acute Vascular Effects of Tamoxifen --- p.6 Chapter 1.3.1.3. --- Chronic Vascular Effects of Tamoxifen --- p.7 Chapter 1.3.1.4. --- Antioxidant Effects of Tamoxifen --- p.8 Chapter 1.3.2. --- Raloxifene --- p.8 Chapter 1.3.2.1. --- Cardiovascular Effects of Raloxifene --- p.8 Chapter 1.3.2.2. --- Acute Vascular Effects of Raloxifene --- p.9 Chapter 1.3.2.3. --- Chronic Vascular Effects of Raloxifene --- p.10 Chapter 1.3.2.4. --- Ovariectomy and Raloxifene Treatment --- p.11 Chapter 1.4. --- Mechanism of Action of SERMs --- p.15 Chapter 1.5. --- Effects of Functional Endothelium and Nitric Oxide --- p.18 Chapter 1.6. --- Dihydropyridine (DHP) Calcium Channel Antagonists --- p.19 Chapter 1.6.1. --- Development of Newer Generation of Dihydropyridines --- p.19 Chapter 1.6.2. --- Effects of Dihydropyridines on Vascular Endothelium (I) --- p.20 Chapter 1.6.3. --- Effects of Dihydropyridines on Vascular Endothelium (II) --- p.21 Chapter 1.6.4. --- Effects of Dihydropyridines on Nitric Oxide Synthase (NOS) --- p.21 Chapter 1.6.5. --- Clinical Studies of Dihydropyridines --- p.22 Chapter 1.7. --- Vascular Ion Channels --- p.25 Chapter 1.8. --- Objectives of The Present Study --- p.26 Chapter Chapter II - --- Materials and Methods Chapter 2.1. --- Tissue Preparation --- p.27 Chapter 2.1.1. --- Preparation of The Porcine Left Circumflex Coronary Arteries --- p.27 Chapter 2.1.2. --- Removal of Functional Endothelium --- p.27 Chapter 2.1.3. --- Organ Bath Setup --- p.27 Chapter 2.1.4. --- Isometric Force Measurement --- p.29 Chapter 2.2. --- In situ Endothelial [Ca2+]i Imaging --- p.29 Chapter 2.2.1. --- Preparation of Porcine Left Circumflex Coronary Arteries --- p.29 Chapter 2.2.2. --- Setup For In situ Endothelial [Ca2+]i Imaging --- p.30 Chapter 2.3. --- Electrophysiological Measurement of BKCa Current --- p.31 Chapter 2.3.1. --- Enzymatic Dissociation of Coronary Artery Smooth Muscle Cells --- p.31 Chapter 2.3.2. --- Electrophysiological Measurement --- p.31 Chapter 2.4. --- DPPH Free Radical Scavenging Assay --- p.31 Chapter 2.5. --- Solutions and Drugs --- p.32 Chapter 2.5.1. --- "Drugs, Chemicals and Enzymes" --- p.32 Chapter 2.5.2. --- Solutions Used in Force Measurement --- p.34 Chapter 2.6. --- Statistical Analysis --- p.34 Chapter Chapter III - --- Tamoxifen-Induced Endothelial Nitric Oxide-Dependent Relaxation in Porcine Coronary Arteries via Ouabain- and BaCl2-Sensitive Mechanisms Chapter 3.1. --- Abstract --- p.35 Chapter 3.2. --- Introduction --- p.36 Chapter 3.3. --- Methods and Materials --- p.37 Chapter 3.3.1. --- Vessel Preparation --- p.37 Chapter 3.3.2. --- Isometric Force Measurement --- p.38 Chapter 3.3.3. --- In situ Endothelial [Ca2+]i Imaging --- p.39 Chapter 3.3.4. --- Chemicals --- p.40 Chapter 3.3.5. --- Data Analysis --- p.40 Chapter 3.4. --- Results --- p.41 Chapter 3.4.1. --- Relaxant Responses --- p.41 Chapter 3.4.2. --- Effects of Inhibitors of NO-Dependent Relaxation --- p.41 Chapter 3.4.3. --- Effects of Putative K+ Channel Blockers and Ouabain --- p.41 Chapter 3.4.4. --- "Effects of Ouabain, Removal of Extracellular K+ Ions and BaCI2" --- p.42 Chapter 3.4.5. --- SNP-Induced Relaxation --- p.42 Chapter 3.4.6. --- Effects of Actinomycin D and Cycloheximide --- p.42 Chapter 3.4.7. --- Relaxant Effect of 17β-Estradiol --- p.43 Chapter 3.4.8. --- Effects on Endothelial [Ca2+]i in Isolated Coronary Arteries With Endothelium --- p.43 Chapter 3.5. --- Discussion --- p.53 Chapter Chapter IV - --- Endothelium-Independent Relaxation to Raloxifene in Porcine Coronary Arteries Chapter 4.1. --- Abstract --- p.57 Chapter 4.2. --- Introduction --- p.58 Chapter 4.3. --- Methods and Materials --- p.59 Chapter 4.3.1. --- Vessel Preparation --- p.59 Chapter 4.3.2. --- Isometric Force Measurement --- p.60 Chapter 4.3.3. --- Electrophysiological Measurement of BKCa Current --- p.61 Chapter 4.3.3.1. --- Enzymatic Dissociation of Coronary Artery Smooth Muscle --- p.61 Chapter 4.3.3.2. --- Electrophysiological Measurement --- p.62 Chapter 4.3.4. --- Chemicals --- p.63 Chapter 4.3.5. --- Data Analysis --- p.63 Chapter 4.4. --- Results --- p.64 Chapter 4.4.1. --- Effect of Raloxifene on Agonist-Induced Contractions --- p.64 Chapter 4.4.2. --- Role of Endothelium --- p.64 Chapter 4.4.3. --- Effect of ER Antagonist --- p.65 Chapter 4.4.4. --- Effect of Putative K+ Channel Blockers --- p.65 Chapter 4.4.5. --- Effect of Elevated Extracellular K+ Concentrations --- p.65 Chapter 4.4.6. --- Effects of Raloxifene on BKCa Current --- p.65 Chapter 4.5. --- Discussion --- p.75 Chapter Chapter V - --- Therapeutic Concentrations of Raloxifene Augment Bradykinin Mediated Nitric Oxide-Dependent Relaxation in Porcine Coronary Arteries Chapter 5.1. --- Abstract --- p.78 Chapter 5.2. --- Introduction --- p.79 Chapter 5.3. --- Methods and Materials --- p.80 Chapter 5.3.1. --- Vessel Preparation --- p.80 Chapter 5.3.2. --- Isometric Force Measurement --- p.80 Chapter 5.3.3. --- In situ Endothelial [Ca2+]i Imaging --- p.81 Chapter 5.3.4. --- Free Radical Scavenging Assay --- p.82 Chapter 5.3.5. --- Chemicals --- p.83 Chapter 5.3.6. --- Data Analysis --- p.83 Chapter 5.4. --- Results --- p.84 Chapter 5.4.1. --- Relaxation to Bradykinin --- p.84 Chapter 5.4.2. --- Effect of Raloxifene on Bradykinin-Induced Relaxation --- p.84 Chapter 5.4.3. --- Effect of Raloxifene on Relaxation Induced by Substance P and --- p.85 Chapter 5.4.4. --- Effect of Estrogen on Bradykinin-Induced Relaxation --- p.85 Chapter 5.4.5. --- Effect of Raloxifene on Sodium Nitroprusside-Induced Relaxation --- p.86 Chapter 5.4.6. --- Free Radical Scavenging Effect --- p.86 Chapter 5.4.7. --- Raloxifene Augmentation of Bradykinin-Stimulated Endothelial [Ca2+]i --- p.86 Chapter 5.5. --- Discussion --- p.99 Chapter Chapter VI - --- "Cilnidipine, a Slow-Acting Ca2+ Channel Blocker, Induces Relaxation in Porcine Coronary Arteries: Role of Endothelial Nitric Oxide and [Ca2+]i" Chapter 6.1. --- Abstract --- p.102 Chapter 6.2. --- Introduction --- p.103 Chapter 6.3. --- Methods and Materials --- p.104 Chapter 6.3.1. --- Vessel Preparation --- p.104 Chapter 6.3.2. --- Isometric Force Measurement --- p.105 Chapter 6.3.3. --- In situ Endothelial [Ca2+]i Imaging --- p.106 Chapter 6.3.4. --- Free Radical Scavenging Assay --- p.107 Chapter 6.3.5. --- Chemicals --- p.108 Chapter 6.3.6 --- Data Analysis --- p.108 Chapter 6.4. --- Results --- p.108 Chapter 6.4.1. --- Relaxant Responses --- p.108 Chapter 6.4.2. --- Role of the Endothelium --- p.109 Chapter 6.4.3. --- Effect of Inhibitors of NO-Dependent Relaxation --- p.109 Chapter 6.4.4. --- Effect of Indomethacin and w-conotoxin --- p.110 Chapter 6.4.5. --- Effect of Cilnidipine on Sodium Nitroprusside-Induced Relaxation --- p.110 Chapter 6.4.6. --- Effects on Endothelial [Ca2+]i in Isolated Endothelium-Intact Coronary Arteries --- p.110 Chapter 6.4.7. --- Free Radical Scavenging Effect --- p.110 Chapter 6.5. --- Discussion --- p.120 Chapter Chapter VII - --- General Summary --- p.123 References --- p.128 Leung, Hok Sum. Chinese University of Hong Kong Graduate School. Division of Physiology. 2005 Text bibliography print xi, 148 leaves : ill. (some col.) ; 30 cm. cuhk:325237 http://library.cuhk.edu.hk/record=b5892728 eng chi Use of this resource is governed by the terms and conditions of the Creative Commons “Attribution-NonCommercial-NoDerivatives 4.0 International” License (http://creativecommons.org/licenses/by-nc-nd/4.0/) http://repository.lib.cuhk.edu.hk/en/islandora/object/cuhk%3A325237/datastream/TN/view/Modulation%20of%20vascular%20reactivity%20by%20selective%20estrogen%20receptor%20modulators%20and%20dihydropyridines%20in%20porcine%20coronary%20arteries.jpghttp://repository.lib.cuhk.edu.hk/en/item/cuhk-325237 |