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Expectorant and antioxidative effects of semen oroxyli.January 2004 (has links)
Chan Yiu-Pong. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2004. / Includes bibliographical references (leaves 98-112). / Abstracts in English and Chinese. / Abstract --- p.i / Acknowledgement --- p.v / Declaration --- p.vi / Table of content --- p.vii / List of Tables --- p.x / List of Figures --- p.xi / List of abbreviation --- p.xiv / Chapter Chapter 1 --- Introduction --- p.1 / Chapter 1.1 --- Introduction of Semen Oroxyli --- p.1 / Chapter 1.1.1 --- Chemical constituents of Oroxylum indicum seed --- p.3 / Chapter 1.1.2 --- Pharmacological studies --- p.3 / Chapter 1.2 --- Introduction to tracheal secretion --- p.6 / Chapter 1.2.1 --- Mucus composition --- p.6 / Chapter 1.2.2 --- Sputum formation --- p.6 / Chapter 1.2.3 --- Expectorant --- p.7 / Chapter 1.2.3.1 --- Secretolytic drugs --- p.7 / Chapter 1.2.3.2 --- Mucolytic drugs --- p.8 / Chapter 1.2.4 --- Assays of studying expectorant activity --- p.10 / Chapter 1.2.4.1 --- Tracheal phenol red secretion system --- p.10 / Chapter 1.3 --- Introduction to oxidant and antioxidant --- p.11 / Chapter 1.3.1 --- Oxidants/ reactive oxygen species --- p.11 / Chapter 1.3.1.1 --- Production of oxidants/ reactive oxygen species --- p.11 / Chapter 1.3.1.2 --- Reactive oxygen species reaction products --- p.12 / Chapter 1.3.1.2.1 --- DNA damage --- p.13 / Chapter 1.3.1.2.2 --- Protein damage --- p.13 / Chapter 1.3.1.2.3 --- Lipid damage --- p.14 / Chapter 1.3.2 --- Antioxidant --- p.14 / Chapter 1.3.2.1 --- Endogenous antioxidants --- p.15 / Chapter 1.3.2.1.1 --- Superoxide dismutase --- p.15 / Chapter 1.3.2.1.2 --- Catalase --- p.15 / Chapter 1.3.2.1.3 --- Glutathione and glutathione peroxidases --- p.15 / Chapter 1.3.3 --- Synthetic and natural antioxidants --- p.16 / Chapter 1.3.3.1 --- Vitamin C --- p.17 / Chapter 1.3.3.2 --- Tocopherols (Vitamin E) --- p.17 / Chapter 1.3.4 --- Assays for studying antioxidative activities --- p.19 / Chapter 1.3.4.1 --- DPPH radical scavenging system --- p.19 / Chapter 1.3.4.2 --- PMS-NADH system --- p.19 / Chapter 1.3.4.3 --- APPH-induced hemolysis system --- p.20 / Chapter 1.4 --- Objectives of the research --- p.22 / Chapter Chapter 2 --- Materials and Methods --- p.24 / Chapter 2.1 --- Materials --- p.24 / Chapter 2.1.1 --- Semen Oroxyli --- p.24 / Chapter 2.1.2 --- Animals --- p.24 / Chapter 2.1.3 --- Chemicals --- p.25 / Chapter 2.2 --- Methods --- p.28 / Chapter 2.2.1 --- Assay for studying expectorant activity --- p.28 / Chapter 2.2.1.1 --- Phenol red standard curve --- p.28 / Chapter 2.2.1.2 --- Tracheal phenol red secretion system --- p.28 / Chapter 2.2.2 --- Assays for studying antioxidative activity --- p.30 / Chapter 2.2.2.1 --- DPPH radicals scavenging system --- p.30 / Chapter 2.2.2.2 --- PMS-NADH system --- p.31 / Chapter 2.2.2.3 --- AAPH-induced red blood cell hemolysis system --- p.32 / Chapter 2.2.3 --- "Extraction, fractionation and purification of Semen Oroxyli" --- p.33 / Chapter 2.2.3.1 --- 70% ethanol extraction of Semen Oroxyli --- p.33 / Chapter 2.2.3.2 --- Fractionation in polyamide column --- p.33 / Chapter 2.2.3.3 --- Fractionation in resin column --- p.34 / Chapter 2.2.3.4 --- Sub-fractions separation from 95% ethanol soluble fraction --- p.34 / Chapter 2.2.3.5 --- Pure compounds obtained from sub-fractions --- p.34 / Chapter 2.2.4 --- Nulcear magnetic resonance (NMR) for identification --- p.38 / Chapter Chapter 3 --- Results of Expectorant Activity --- p.39 / Chapter 3.1 --- Expectorant Activity --- p.39 / Chapter 3.1.1 --- Expectorant Activity on Semen Oroxyli ethanol extract --- p.39 / Chapter 3.1.2 --- Expectorant activities of fractionations of Semen Oroxyli ethanol extract --- p.39 / Chapter Chapter 4 --- Results of Antioxidative Activity --- p.44 / Chapter 4.1 --- Antioxidative activity --- p.44 / Chapter 4.1.1 --- Antioxidative activity of 70% ethanol extract --- p.44 / Chapter 4.1.2 --- Antioxidative activity of fractions of 70% ethanol extract --- p.49 / Chapter 4.1.3 --- Antioxidative activity on sub-fractions fractionated from 95% ethanol-soluble fraction --- p.50 / Chapter 4.1.4 --- Antioxidative activity on pure compounds isolated from sub-fractions --- p.59 / Chapter Chapter 5 --- Results of Identification of Pure compounds --- p.68 / Chapter 5.1 --- Identification of compounds --- p.68 / Chapter 5.1.1 --- Compound A --- p.68 / Chapter 5.1.2 --- Compound B --- p.69 / Chapter 5.1.3 --- Compound C --- p.69 / Chapter 5.1.4 --- Compound D --- p.70 / Chapter 5.1.5 --- Compound E --- p.71 / Chapter Chapter 6 --- Discussion --- p.73 / Chapter 6.1 --- Discussion of expectorant activity of Semen Oroxyli --- p.73 / Chapter 6.2 --- Discussion of antioxidative activity of Semen Oroxyli --- p.75 / Chapter 6.3 --- General Discussion --- p.77 / Chapter Chapter 7 --- Conclusions --- p.82 / Appendix A Procedures for preparing the phenol red standard curve for tracheal phenol red secretion system. --- p.85 / Appedix B 1H NMR and 13C NMR spectra --- p.87 / References --- p.98
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Toward the Refinement of Expiratory Muscle Strength Training for Cough and Swallowing RehabilitationDakin, Avery January 2024 (has links)
Expiratory muscle strength training (EMST) is a resistance exercise targeting the expiratory musculature that has predominated rehabilitation research for cough and swallowing. While there have been consistent improvements in expiratory muscle strength with EMST, and promising findings in cough and swallowing, there remains a substantial gap in our understanding of the physiologic adaptations associated with training and how to optimize rehabilitative outcomes. This dissertation consists of two studies aimed at refining EMST protocols for cough and swallowing rehabilitation.
Chapter 1 is an introduction that provides an overview of exercise prescription principles, outlines what is known related to exercise protocols and EMST outcome measures, and finally describes the current research gaps and dissertation aims. Chapter 2 focuses on quantifying the relationship between resistive load and ratings of perceived exertion (RPE) during EMST, examines variability in RPE in healthy adults, and compares RPE using two respiratory devices.
In Chapter 3, we examine the impact of modifying exercise parameters on physiologic adaptations and RPE, while also beginning to establish links between EMST, cough, and swallowing by assessing task specificity. Chapter 4 synthesizes the research findings into the greater scientific literature, discusses the clinical implications of this work, outlines limitations, and suggests avenues for future research.
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Chemical and pharmacological investigations into an antitussive traditional Chinese medicinal herb. / CUHK electronic theses & dissertations collectionJanuary 2001 (has links)
Chung Hoi Sing. / "August 2001." / Thesis (Ph.D.)--Chinese University of Hong Kong, 2001. / Includes bibliographical references (p. 186-204) / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Mode of access: World Wide Web. / Abstracts in English and Chinese.
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Antitussive alkaloids of stemona tuberosa. / CUHK electronic theses & dissertations collectionJanuary 2006 (has links)
Bioassays of total alkaloids of S. tuberosa samples representing the four types of chemical profiles were conducted on guinea pigs using citric acid aerosol for inducing cough. These results demonstrated their antitussive properties and thus suggested the possibility of other antitussive alkaloids than neotuberostemonine in S. tuberosa. So it became necessary to identify the major components in the samples of S. tuberosa representing the four types of chemical profiles. / Bioassays on guinea pigs of the four major components of S. tuberosa demonstrated their antitussive properties. Except a lower potency in tuberostemonine, antitussive effects of croomine and stemoninine showed similar or even stronger potency than neotuberostemonine at 25 and 50 mg/kg by intragastric administration. These four antitussive alkaloids could be used as lead compounds for the development of new antitussive drugs and as bioactive markers in quality control of the herb S. tuberosa and related products. / Cough is an airway defensive reflex, which is responsible for keeping the airway free of obstruction and harmful substances. As the commonest symptom for which medical advices is sought, enormous costs are spent on cough treatments. Regretfully, currently used antitussives are less than satisfactory due to their low potency or obvious side effects. So it is necessary to continue developing new and better antitussives. / Electrical stimulation of the superior laryngeal nerve on guinea pigs at 100 mg/kg through intraperitoneal administration indicated that croomine acted on the central pathway of cough reflex accompanied by respiratory depression. On the other hand, neotuberostemonine, tuberostemonine and stemoninine acted on the peripheral pathway without any observable side effects. These three alkaloids could be promising for developing new peripherally acting antitussives. Further, tuberostemonine was tested on primary cultured nodose ganglion cells by patch clamp and, at 0.5 mM, was demonstrated to significantly decrease the change amplitude of membrane potential induced by 1.0 mM citric acid solution. The results suggested that tuberostemonine could depress electrical excitability of nodose ganglion cells and thus inhibit the afferent signals of cough reflex leading to its antitussive activity. / In order to determine if the different chemical profiles of Stemona total alkaloids were the result of species difference or variations within the same species, the three Stemona species registered in the PRC Pharmacopoeia were collected from different areas in China. They were planted to flowering in our greenhouse and authenticated by both reproductive and vegetative characters. Microscopic examination on these authentic species showed that tuberous roots of S. tuberosa differed by epidermal cells with smooth outer surface and fibers in the cortex and pith from those of S. japonica and S. sessilifolia. The chemical profiles of authentic samples were analyzed on a HPLC-ELSD system. The results indicated that species-specific differences were present in the HPLC profiles of the three Stemona species. Within S. tuberosa, the chemical profiles of different samples were found to be very variable and they could be roughly divided into four types in the tested samples. Neotuberostemonine was present in one of the four types of S. tuberosa. Since antitussive effects of neotuberostemonine were demonstrated by Chung et al. (2003), it became necessary to determine if the samples containing alkaloids other than neotuberostemonine had antitussive properties. / The Chinese herb Radix Stemonae (Baibu) has long been used as an antitussive in Chinese medicine for some two thousand years. Its source materials, according to the Pharmacopoeia of the People's Republic of China (PRC Pharmacopoeia), come from the tuberous roots of three Stemona species, namely, S. japonica (Blume) Miq., S. sessilifolia (Miq.) Miq. and S. tuberosa Lour. However, hardly any experimental study is available to document their antitussive functions. Chung et al. (2003) reported that the antitussive components of S. tuberosa were neotuberostemonine and related stenine type Stemona alkaloids. And the antitussive potency of neotuberostemonine through intraperitoneal administration was reported to be comparable to codeine but not involving opioid receptors. In continuation with the study of the antitussive properties of the herb, it was found that total alkaloids of different samples of the herb appeared to vary in chemical profiles, whereas neotuberostemonine was found in only a few samples. / The major components of S. tuberosa including stemoninine, croomine and neotuberostemonine were isolated and determined by spectroscopic methods. It was the first time to isolate croomine from Stemona species, lending support to retaining the two genera Stemona and Croomina in the family Stemonaceae according to chemotaxonomy. Tuberostemonine, another major component of S. tuberosa was also isolated and determined in our team. Neotuberostemonine and tuberostemonine were two isomers but mutually exclusive in our tested samples. Moreover, these major components of S. tuberosa belonged to three types in molecular structure. Stemoninine was stemonamide type, croomine tuberostemospironine type and both neotuberostemonine and tuberostemonine stenine type. These results suggested that antitussive effects of S. tuberosa might be related to the components belonging to these three molecular types. / Xu Yantong. / "March 2006." / Adviser: Paul But. / Source: Dissertation Abstracts International, Volume: 67-11, Section: B, page: 6231. / Thesis (Ph.D.)--Chinese University of Hong Kong, 2006. / Includes bibliographical references (p. 137-155). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstracts in English and Chinese. / School code: 1307.
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Chemical, pharmacological and intestinal absorption studies of stemona alkaloids from radix stemonae. / CUHK electronic theses & dissertations collectionJanuary 2006 (has links)
Finally, intestinal absorption of compounds A and H were also investigated by Caco-2 monolayer cell model. These results demonstrated, for the first time, that these stemona alkaloids were well absorbed in a gastrointestinal cell culture model. Furthermore, compound A was demonstrated to have a marked preference in the basolateral to apical transport direction, and such efflux (basolateral to apical) transport was inhibited by both verapamil and cyclosporine A, P-glycoprotein (P-gp) inhibitors, but not by probenecid and MK371, multidrug resistant-associated protein (MRP) inhibitors. The results suggested that compound A transported through active efflux mechanisms via P-gp but not MRP pathway. / High performance liquid chromatography (HPLC) coupled with evaporative laser scattering detector (ELSD) was developed to qualitatively and quantitatively determine the chemical profiles of Radix Stemonae. The results demonstrated that the type and quantity of the main bioactive ingredients, stemona alkaloids, present in various herbal samples varied significantly. Compound A (neotuberostemonine) was identified as a predominant alkaloid in two commercial Radix Stemonae samples, whereas compound F (croomine), compound H (tuberostemonine) and compound G (oxoneotuberostemonine) were identified as the major alkaloids present in other three commercial samples, respectively. Chemical variations were observed in several fresh Radix Stemona samples collected in mainland China. These chemical variations might be due to species and/or environmental differences. / In addition to the antitussive activities, it was found that a high dose of compound A caused markedly behavioral changes, including head and body shaking via both intraperitoneal and intracerebroventricular administration. Such adverse effect was abolished by a centrally acting dopamine D2 antagonist haloperidol, suggesting that a central dopaminergic effect might contribute to the behavioral activities produced by compound A. Moreover, compound A was found, for the first time, to dose-dependently and competitively inhibit monoamine oxidase (MAO)-B and compound A was identified to be a weak and non-competitively inhibitor on MAO-A. It was further demonstrated that compound A increased the intercellular concentration of dopamine in the cultured PC12 cells and prevented MPTP-induced cell death in PC12 cells via inhibition of MAO. Therefore, the behavioral changes induced by compound A was suggested to be involved with dopaminergic pathway via reduction of dopamine metabolism caused by inhibition of MAO. / On the other hand, compound F was demonstrated to cause acute lethal toxicity via intraperitoneal but not via oral administration. The results suggested that compound F might have a low oral bioavaiIability. Further absorption study by Caco-2 model demonstrated that this alkaloid had a good intestinal absorption, thus its low oral bioavailability could be due to extensive first-pass effects in the gastrointestinal tract. / Pharmacological properties of stemona alkaloids were studied in vivo using the citric acid-induced guinea pig cough model. The three stemona alkaloids present in different Radix Stemonae samples were all found to be antitussive. Compounds A and H were both orally active and had similar antitussive potencies via both oral and intraperitoneal (i.p.) administrations. Compound F was demonstrated to be antitussive via i.p. administration only. The mechanism of antitussive activity of the representative stemona alkaloid, compound A, was further investigated. However, none of the currently known antitussive pathways were identified to be involved in compound A. Thus, compound A and also other stemona alkaloids are likely to produce their antitussive activity via a novel pathway. / Radix Stemonae is derived from the root tubes of three different species of Stemona genus (Stemonaceae). This herb has been prescribed in traditional Chinese medicine (TCM) as an antitussive agent for over thousands of years. To date, over fifty stemona alkaloids have been identified from various Stemona species. However, there is a lack of direct evidence to link stemona alkaloids to the effectiveness of the herb in the treatment of cough. The aim of the present study is to investigate Stemona species used as plant sources for Radix Stemonae, the chemical and pharmacological properties in relation to antitussive activity of the herb, and the intestinal absorption of the main bioactive constituents, stemona alkaloids, in the herb. / The identity of fresh Radix Stemonae samples was investigated using a DNA based polymorphism assay. 5S-rRNA, ITS-1 and ITS-2 are highly conserved spacer regions; thus, the diversity of these spacer regions was used for the identification of Radix Stemonae samples. The amplified spacer regions of different Radix Stemona samples collected from different geographical locations in Mainland China were sequenced and compared. The result demonstrated that there were at least three different DNA patterns among seven samples examined and this DNA sequential assay could distingue species in Stemona genus from species in other genera. However, the findings suggested that the variation in chemical profiles of different Radix Stemonae samples was not directly related to their DNA sequences. DNA sequential method could be used to authenticate the correct plant sources for Radix Stemonae but it can not to provide information on chemical profiles of the herb. / The overall results demonstrated that the quantities and types of stemona alkaloids varied significantly depending upon plant sources. Furthermore, these stemona alkaloids differed considerably in pharmacological activities, toxicological effects and absorption profiles. Therefore, these variations in different Radix Stemonae samples may lead to different therapeutic outcomes, including efficacies, adverse effects, and potential herb-drug and herb-herb interactions. Nevertheless, the present study provided a scientific basis for the therapeutic use of Radix Stemonae and illustrated a potential for the development of herbal Radix Stemonae or pure stemona alkaloids into a new class of antitussive TCM herbal products or TCM-based agents in the future. / Leung Pak Ho Henry. / "January 2006." / Adviser: Ge Lin. / Source: Dissertation Abstracts International, Volume: 67-11, Section: B, page: 6328. / Thesis (Ph.D.)--Chinese University of Hong Kong, 2006. / Includes bibliographical references (p. 179-197). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstracts in English and Chinese. / School code: 1307.
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