Table of Contents
COVER
TITLE PAGE
COPYRIGHT PAGE
DEDICATION
FOREWORD
PREFACE
CONTRIBUTORS
1 POLYPHENOLS AND FLAVONOIDS: AN OVERVIEW
1.1 INTRODUCTION
1.2 SYNTHESIS
1.3 SOURCES
1.4 PHARMACOLOGICAL ACTIVITIES OF SELECTED FLAVONOIDS
1.5 CONCLUSIONS
REFERENCES
2 ANALYSIS OF FLAVONOIDS THROUGH CHROMATOGRAPHY
2.1 INTRODUCTION
2.2 POLYPHENOLS
2.3 CHROMATOGRAPHY
2.4 DETECTION
2.5 METHOD DEVELOPMENT
2.6 VALIDATION
2.7 SUMMARY
2.8 FUTURE DIRECTIONS
2.9 CONCLUSIONS
REFERENCES
3 CHIRAL METHODS OF FLAVONOID ANALYSIS
3.1 INTRODUCTION
3.2 FLAVONOIDS AND CHIRALITY
3.3 SEPARATION OF ENANTIOMERS THROUGH CHROMATOGRAPHY
3.4 ENANTIOMERIZATION AND RACEMIZATION
3.5 CURRENT METHODS: PROS AND CONS
3.6 FLAVANONES
3.7 CATECHINS
3.8 CONCLUSIONS
REFERENCES
4 PRECLINICAL PHARMACOKINETICS OF FLAVONOIDS
4.1 INTRODUCTION
4.2 ABSORPTION
4.3 DISTRIBUTION
4.4 METABOLISM
4.5 EXCRETION
4.6 CONCLUSIONS
REFERENCES
5 CLINICAL PHARMACOKINETICS OF FLAVONOIDS
5.1 INTRODUCTION
5.2 METHODS OF ANALYSIS
5.3 FLAVONOID PHARMACOKINETICS
5.4 DRUG INTERACTIONS
5.5 CONCLUSIONS
REFERENCES
6 TOXICOLOGY AND SAFETY OF FLAVONOIDS
6.1 INTRODUCTION
6.2 FLAVONOIDS AND THE GASTROINTESTINAL TRACT
6.3 FLAVONOIDS AND HEPATIC SIDE EFFECTS
6.4 FLAVONOIDS AND THE KIDNEY
6.5 FLAVONOIDS AND BLOOD DISORDERS
6.6 FLAVONOIDS AND CANCER
6.7 FLAVONOIDS AND THE ENDOCRINE SYSTEM
6.8 FLAVONOIDS AND OCULAR SAFETY
6.9 FLAVONOIDS AND THE CENTRAL NERVOUS SYSTEM
6.10 ALLERGY-LIKE RESPONSES AND FLAVONOIDS
6.11 FLAVONOIDS AND PREGNANCY
6.12 OVERVIEW AND CONCLUSIONS
REFERENCES
7 FLAVONOIDS AND DRUG INTERACTIONS
7.1 INTRODUCTION
7.2 FLAVONOID–DRUG INTERACTIONS MEDIATED BY FOOD, BEVERAGE, AND HERBAL INTAKE
7.3 BEVERAGE INTAKE
7.4 FOOD INTAKE
7.5 FLAVONOID–DRUG INTERACTIONS
7.6 FLAVONOID–DRUG INTERACTIONS MEDIATED BY TRANSPORTERS
7.7 EXPERIMENTAL TECHNIQUES TO STUDY FLAVONOID–ABC TRANSPORTER INTERACTIONS
7.8 P-GLYCOPROTEIN (P-GP, ABCB1)
7.9 INTERACTION BETWEEN P-GLYCOPROTEIN AND CYP450
7.10 MULTIDRUG RESISTANCE PROTEIN 2 (MRP2, ABCC2)
7.11 BREAST CANCER RESISTANCE PROTEIN (BCRP, ABCG2)
7.12 FLAVONOID MODULATION OF ABC TRANSPORTER EXPRESSION
7.13 ORGANIC ANION TRANSPORTERS (OATS)
7.14 CYTOCHROME P450
7.15 CONCLUSIONS
REFERENCES
INDEX
Copyright © 2013 by John Wiley & Sons, Inc. All rights reserved
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Published simultaneously in Canada
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ISBN: 9780470578711
Dedicated to my wife Claudia Davies
and daughters Cassandra, Daniela, and Catalina,
who have encouraged and supported me throughout the journey.
—Neal M. Davies
Dedicated to my mother Lillian Emperatriz Farfán Azpilcueta
and my grandmother Hilda Regina Farfán Aspilcueta,
whose inspirations live on with this book,
and to all my family for their
unconditional love, encouragement,
and understanding.
—Jaime A. Yáñez
FOREWORD
Natural products have been used for hundreds and even thousands of years as food products and for therapeutic benefit. Even today a large part of the world’s population relies on plants for their well-being. What at first may seem surprising is that natural products continue to be popular in developed countries, including the US, Canada, Australia, the UK, and Europe. However, this becomes understandable when one considers the factors that have led to the interest in and the continuing development of natural products in the marketplace. Among these are concerns associated with development of pharmaceuticals, particularly the increasing cost of maintaining a pipeline and bringing the small number of successful molecules to market. Developed societies continue to look toward natural products for many reasons, including a desire to maintain more control of their health care into older age, particularly given the greater awareness of side effects that have become apparent with some recently introduced drugs. Despite the explosion of biotechnology, the pharmaceutical industry continues to utilize natural products for small molecule drug discovery, and over half of small drug molecules available today continue to have their origins in natural products. The science behind natural products thus continues to be important and, indeed, essential if such agents are to continue to be used safely and effectively and as sources of new discoveries and therapies.
Polyphenols are being recognized more and more as important components of plant natural products. There are some striking examples of the importance of such agents in health care, including components of green tea, red wine, and chocolate for cardiovascular disease protection and as adjunctive cancer management. There are thousands of such compounds present in plants, and to date we have only just begun to identify a relatively small percentage of such molecules from a small percentage of plants that have been screened from nature’s bounty. Among the polyphenols are the group of molecules known as flavonoids. While thousands of flavonoids have been identified many more remain unknown and undiscovered. The potential for understanding the scientific basis of traditional medicine and for developing new therapies based on flavonoids remains enormous.
Advances in natural products must be based on the use of a multitude of techniques and practices. Greater application of research methodologies is key to such development. Only through understanding the structure and function relationships of molecules such as the flavonoids can we hope to apply what is commonly described as “reverse pharmacology”—that is, the discovery and improvement of therapies starting from traditional knowledge built over many generations in many cultures and then designing chemical, pharmacological, and clinical studies to validate and extend the value and understanding of such therapies in the context of today’s requirements for evidence-based therapeutic approaches.
This book covers the fundamental techniques that can be applied to natural product research and describes the science and methodology behind these techniques. It then provides extensive examples of the outcomes from applications of these techniques. Before the new chemical entities can be described, a variety of experimental methods of isolation, separation, and identification are needed—a complex process in natural medicines where one expects multi-component and multi-target actions underpinning clinical effectiveness. Furthermore, such understanding of the chemistry of flavonoids is essential if new molecules can be developed to overcome normal limitations of natural products and, hence, to provide wider application in modern therapy. Principles that are common in pharmaceutical research, such as identifying metabolism and describing the role of chirality of natural products, are demonstrated in this scientific evaluation; and flavonoids provide excellent examples of this. Only certain molecules have a primary role in many herbal medicines, while other components support the clinical effectiveness of the herb (such as moderating absorption and reducing toxic effects). The molecules responsible for all these attributes are often unknown. As an example, willow bark is used for arthritis and pain; yet, while it is known that salicyn is a major component and a source of salicylic acid, it has become evident that the levels of salicylate produced in the body are insufficient to explain the clinical results. Hence, one must search for other perhaps minor, but potent, components which account for the efficacy of willow bark. These may well be flavonoids and other components known to be also present in the preparations, given the wide range of pharmacological actions that have been described for such compounds.
A major limitation of herbal natural product medicines for current therapeutic applications is the bioavailability of their various components. Thus the effects obtained with natural medicines are generally slow to develop, often require high concentrations, and generally produce milder effects compared to, say, analgesics like paracetamol or aspirin (as is the case in the willow bark example above). Understanding metabolism and pharmacokinetics of the natural product components is key to understanding and ultimately improving the effectiveness of natural products, while still maintaining the benefits of their lower toxicity. This is an emerging and less-researched area of natural medicines, and the authors of this book are world experts in this specialized pharmaceutical area. They provide an excellent rationale for the experimental methods required in undertaking pharmacokinetic experiments, including the ADME parameters of absorption, distribution, metabolism, and excretion. They follow this up with a comprehensive list of examples of pharmacokinetic studies that have been undertaken preclinically and clinically in the flavonoid area. This is a major and important contribution of this book. Such studies also lead to the appropriate use of natural products, particularly with respect to the potential for interactions, both positive and negative, between herbal natural medicines and pharmaceutical drugs and other foods and supplements. In my own research, we have undertaken development of an herb–drug interaction database on such interactions; and this book provides an excellent source for studies of such interactions.
Overall, natural product state-of-the-art research is continuing to grow; and the need for more sophisticated research is growing. Flavonoids is an important class of molecules in natural medicines and various other complementary medicine products which, while appreciated for a long time, rely on state-of-the-art methodology for their understanding and for new discoveries. Having a source of information on underpinning scientific methodology and extensively documented natural product research outcomes, as provided by this book, will be invaluable for all those interested in this area or wanting to gain a greater appreciation of the potential of this approach.
BASIL D. ROUFOGALIS, PhD, DSc
Professor Emeritus
University of Sydney
PREFACE
There has been an increase in pharmaceutical and biomedical therapeutic interest in natural products as reflected in the sales of nutraceuticals and functional foods and in the global therapeutic use of traditional medicines over the last decade. The use of traditional medicines is based on knowledge, skills, and practices founded on experiences and theories from different cultures. Traditional medicines are used to prevent and maintain health, which may ultimately improve and/or treat physical and mental illnesses. The present day use of these products encompasses almost every aspect of our daily lives from health and beauty, dietary supplements, performance enhancement supplements, and food and beverage to overall health and well-being products. Over the last 30 years, scientific investigations have illustrated the therapeutic bioactivity of flavonoids in chronic disease studies and have piqued the interests of scientists from the diverse fields of nutrition, food, horticulture, and pharmaceutical sciences. Additionally, increased interest by nutraceutical manufacturers has created an abundance of flavonoid-containing dietary supplements on the market. These products and others like them are consumed by a large percentage of the Western population. Since dietary supplements are viewed by most regulatory agencies as food rather than drugs, many of these products are produced without having passed standards of safety or efficacy. The use of flavonoid-containing nutraceuticals presents a potential public health risk that could be ameliorated by flavonoid-specific research generated from a variety of fields. Hence, the objective of this book is to provide the framework for fundamental concepts and contemporary practice of methods of analysis for achiral and chiral flavonoids, preclinical and clinical pharmacokinetics, as well as toxicology and safety of flavonoids and their possible drug interactions.
It is our belief that this book provides the basic concepts to a novice graduate student and the advanced knowledge to a veteran pharmaceutical, food, or nutrition scientist. Chapter 1 provides a comprehensive overview of polyphenols and flavonoids. The methods of analysis of achiral flavonoids using chromatography are covered in Chapter 2, while methods of analysis for chiral flavonoids are described in Chapter 3. Chapters 4 and 5 present the advanced concepts of preclinical and clinical pharmacokinetics of flavonoids, respectively. The toxicology and safety of flavonoids is presented in Chapter 6, while the reported flavonoid–drug interactions are detailed in Chapter 7. The various topics of this book can be adapted by scientists to their specific research needs.
This book contains diverse topics that required a multidisciplinary effort, which would not have been possible without the great efforts of our contributors. We really appreciate the expertise, willingness, and patience of our contributors during the completion process of this book project. We would like to express our sincere thanks to Mr. Jonathan Rose for his support, patience, and confidence in us. We would also like to express our appreciation to our families and colleagues for their support and encouragement. Finally, we would like to thank Professor Basil Roufogalis, an innovator and world leader in herbal medicine research and education, for writing such an inspiring foreword for this book.
NEAL M. DAVIES, PhD
JAIME A. YÁÑEZ, PhD
CONTRIBUTORS
Preston K. Andrews, Department of Horticulture and Landscape Architecture, Washington State University, Pullman, WA, USA
Nagendra V. Chemuturi, Drug Metabolism and Pharmacokinetics, Alcon Research, Ltd., a Novartis Company, Fort Worth, TX, USA
Neal M. Davies, Faculty of Pharmacy, University of Manitoba, Winnipeg, Manitoba, Canada
Karen D. Gerde, College of Pharmacy, Department of Pharmaceutical Sciences, Washington State University, Pullman, WA, USA
Stephanie E. Martinez, Faculty of Pharmacy, University of Manitoba, Winnipeg, Manitoba, Canada
Connie M. Remsberg, Division of Clinical Pharmacology and Experimental Therapeutics, University of California, San Francisco, CA, USA
Jonathan K. Reynolds, College of Pharmacy, Department of Pharmacotherapy, Washington State University, Pullman, WA, USA
Casey L. Sayre, Faculty of Pharmacy, University of Manitoba, Winnipeg, Manitoba, Canada
Jody K. Takemoto, John A. Burns School of Medicine, Department of Cell and Molecular Biology, University of Hawaii, Honolulu, HI, USA
Karina R. Vega-Villa, College of Pharmacy, The University of Oklahoma, Oklahoma City, OK, USA
Scott W. Womble, Drug Metabolism and Pharmacokinetics, Alcon Research, Ltd., a Novartis Company, Fort Worth, TX, USA
Jaime A. Yáñez, Drug Metabolism and Pharmacokinetics, Alcon Research, Ltd., a Novartis Company, Fort Worth, TX, USA
1
POLYPHENOLS AND FLAVONOIDS: AN OVERVIEW
Jaime A. Yáñez, Connie M. Remsberg, Jody K. Takemoto, Karina R. Vega-Villa, Preston K. Andrews, Casey L. Sayre, Stephanie E. Martinez, and Neal M. Davies
1.1 INTRODUCTION
There has been an increase in pharmaceutical and biomedical therapeutic interest in natural products as reflected in sales of nutraceuticals and in the global therapeutic use of traditional medicines.1–9 Use of traditional medicines is based on knowledge, skills, and practices based on experiences and theories from different cultures that are used to prevent and maintain health, which may ultimately improve, and/or to treat physical and mental illnesses.10 The popularity of these products encompasses almost every aspect of our daily lives from health and beauty, dietary supplements, performance enhancement supplements, food and beverage to overall health and well-being products.1 It is apparent that this growing demand for phytotherapies could be very profitable for nutraceutical and pharmaceutical companies. Nutraceutical as well as pharmaceutical companies are interested in many of these naturally occurring compounds that can be extracted from plants and be further modified, synthesized, formulated, manufactured, marketed, and sold for their reported health benefits. Pharmaceutical companies are also using these natural compounds as lead drug candidates that can be modified and formulated to be potential new drug candidates. From drug discovery and development to marketing, between 15 and 20 years may lapse with billions of dollars spent on drug development and research of pharmaceuticals.11,12 Consumers are looking for beneficial health-related products that have efficacy at a low cost to the consumer, while the nutraceutical industry is struggling to develop therapies at a low cost and to bring them to the market. Through scientific studies, natural products can be scrutinized using pharmaceutical approaches to develop and provide alternative or adjunctive therapies.
The drug discovery process is expensive and time-consuming. It has been estimated to take 10–15 years and $800 million to get a drug to the approval process.13 Part of this cost is due to advances in technology whereby drug manufacturers have adopted a target-based discovery paradigm with high throughput screening of compound libraries. This approach, although expected to have vast potential, has not necessarily proven itself. Reviews of new chemical entities have shown that natural products or derivatives of natural products are still the majority of newly developed drugs. For instance, 63% of the 974 new small molecule chemical entities developed between 1981 and 2006 were directly isolated from nature or semisynthetic derivatives of a natural product.14 This trend continues even into this century where approximately 50% of new small molecule chemical entities approved from 2000 to 2006 have a natural origin.14 It is apparent that natural products are important compounds to be explored in the drug discovery process. More importantly, however, there remains a multitude of bioactive compounds yet to be systematically characterized. It is estimated that of the 250,000–750,000 higher plant species, only 10–15% have been screened for potential therapeutic agents.15 Characterizing bioactive molecules in microbial and marine life is even more limited. Nonetheless, natural products remain a reservoir of potential therapeutic agents.
It has been reported that 5000–10,000 compounds are screened before a single drug makes it to the market, and on average, it takes 10–15 years to develop a single drug.16 Of the successfully developed drugs, 60% have a natural origin, either as modified or unmodified drug entities, or as a model for synthetic drugs—not all of them used for human diseases—and it is estimated that 5–15% of the approximately 250,000–750,000 species of higher plants have been systematically screened for bioactive compounds.15 Structure–activity relationship (SAR) programs are generally employed to improve the chances of phytochemicals being developed as drug entities.17 Further studies to develop more drugs of natural origin have been limited in part due to their structural complexity, which is sometimes incompatible with high throughput formats of drug discovery and high extraction costs.16 The potentially long resupply time and unforeseen political reasons such as warfare in developing nations also limit the development of plant-based drugs.17 As a result, plants remain and represent a virtually untouched reservoir of potential novel compounds. Nevertheless, the number of drugs developed each year based on natural products has remained constant over the last 22 years.17
A class of molecules with well-documented therapeutic potential is the polyphenols. Polyphenols are small molecular weight (MW) compounds (MW 200–400 g/mol) that occur naturally. They are produced as secondary metabolites that serve to protect the plant from bombardment of pathogens and ultraviolet (UV) radiation. Upon environmental threat, the plant host activates one of the synthesis pathways and polyphenol structures are produced and subsequently secreted.18 Which specific polyphenol is produced depends largely on its host, the region of origin, and the environmental stimuli. Many polyphenols are synthesized by the phenylpropanoid pathway. Several classes of polyphenols exist including flavonoids, stilbenes, isoflavonoids, and lignans. Polyphenols of all classes are found in a wide range of plants and plant by-products such as herbal supplements and beauty products.
1.2 SYNTHESIS
An understanding of the biosynthesis of natural compounds will enable researchers to further investigate possible therapeutic uses based on the activity of phytochemicals in plants. Plant chemicals are often given the moniker “phytochemicals” and can be classified either as primary or secondary metabolites.19 Primary metabolites are widely distributed in nature and are needed for physiological development in plants. On the other hand, secondary metabolites are derived from the primary metabolites, are limited in distribution in the plant kingdom, and are restricted to a particular taxonomic group (Fig. 1.1). Secondary metabolites usually play an ecological role; for example, they act as pollinator attractants, are involved in chemical defense, are often end products from chemical adaptations to environmental stresses, or are synthesized in specialized cell types at different developmental stages of plant development or during disease or are induced by sunlight.19
Allelochemicals are phytotoxic compounds produced by higher plants that include flavonoids. Like other secondary metabolites, flavonoids have complex structures where multiple chiral centers are common.19 Flavonoids consist of a C15 unit with two benzene rings A and B connected by a three-carbon chain (Fig. 1.2). This chain is closed in most flavonoids, forming the heterocyclic ring C; however, chalcones and dihydrochalcones present as an open ring system.20 Depending on the oxidation state of the C ring and on the connection of the B ring to the C ring,21 flavonoids can be classified into various subclasses. Flavonoids can undergo hydroxylation, methylation, glycosylation, acylation, prenylation, and sulfonation; these basic chemical metabolic substitutions generate the different subclasses: flavanols, flavanones, flavones, isoflavones, flavonols, dihydroflavonols, and anthocyanidins.20,21 Flavonoids in nature are naturally most often found as glycosides and other conjugates; likewise, many flavonoids are polymerized by plants themselves or as a result of food processing.21
1.2.1 Synthesis of Flavonoids
In plants, primary metabolites such as sugar are associated with basic life functions including, but not limited to, cell division, growth, and reproduction.22 On the other hand secondary metabolites are involved in the adaptive necessity of plants to their environments, such as pigmentation, defense from toxins, and enzyme inhibition;23–25 additionally, these secondary metabolites can have pathogenic or symbiotic effects.26 Secondary metabolites including polyphenols have been associated with having many health benefits.27 The abundance of polyphenols in foodstuffs is apparent, although they often have not been adequately characterized; however, an assortment of polyphenols is prevalent in unprocessed and processed foods and beverages and nutraceuticals.28
Structurally, polyphenols or phenolics have one or more aromatic rings with hydroxyl groups and can occur as simple and complex molecules.29 Polyphenols can be subdivided into two major groups: hydroxybenzoic acids and hydroxycinnamic acids (Fig. 1.3). Examples of hydroxybenzoic acids include gallic and vanillic acids. They are typically found in the bound form as a smaller entity of a ligand or tannin or are linked to a sugar or an organic acid in plant foods.25 Alternatively, hydroxycinnamic acid examples include p-coumaric and caffeic acids. These molecules are found esterified with small molecules, bound to cell walls, and/or proteins.25 A subcategory of p-coumaric acid derivatives is the flavonoids (flavonones, flavanones, flavonols, flavanols [proanthocyanidins, catechins, epicatechins, procyanidins, prodelphinidins], and anthocyanins) as these are the most abundant polyphenols in our diets (Fig. 1.4).30,31 Flavonones and isoflavones can be predominantly found in citrus fruits and soy products, respectively. Proanthocyanidins are complex polymeric flavanols found in conjunction with flavanol catechins from apples, pears, grape, and chocolate products; these flavonoids are primarily responsible for the astringency of foods. Anthocyanins are located in an assortment of fruits (cherries, plums, strawberries, raspberries, blackberries, and currants). In addition to these polyphenol subclasses, in nature, flavonoids are also prevalent as a glycoside (parent compound or aglycone with a sugar moiety attached) as this sugar moiety helps to facilitate water solubility and transportability of the aglycone.26,32,33 Another important factor to consider is that the distribution of polyphenols in plant tissues is heterogenous; thus, the seed, pericarp, flavedo, and albedo contain polyphenols in different proportions.31
Flavonoids are synthesized via the phenylpropanoid pathway and are derived from estrogen.34 The phenylalanine structure from phenolic compounds is transformed to cinnamate by the enzyme phenylalanine ammonia-lyase (PAL). The cinnamate 4-hydroxylase (C4H) converts cinnamate to p-coumarate, and then an acetyl-CoA group is added by the CoA ligase enzyme to yield cinnamoyl-CoA. Lastly, this product is transformed by chalcone synthase (CHS) to yield a general chalcone structure. Stilbenoids are synthesized in much the same fashion except for the C4H enzymatic step (Fig. 1.5).
The chalcone structure is further metabolized by the chalcone isomerase (CHI) to the general chiral flavanone structure. From the general chiral flavanone structure, the other derivatives, namely, dihydroflavonols, flavonols, flavones, flavan-3-ols, flavan-3,4-diols, isoflavonoids, and neoflavonoids, are further metabolized by a well-characterized enzymatically derived process (Fig. 1.6). Anthocyanidins and anthocyanins are derived from flavan-3,4-diols by leuocyanidin oxygenase (LO) and anthocyanidins-3-O-glucosyltransferase, respectively. Chromones are synthesized from isoflavonoids through the chromone synthase (ChS), while lignans and coumarins are derived from neoflavonoids by lignan synthase (LS) and coumarin synthase (CS), respectively (Fig. 1.6).
In addition to flavanone, other small natural compounds found in a wide variety of food and plant sources exist. These compounds, namely, flavonoids, isoflavonoids, and lignans, have generated much scientific interest in their potential clinical applications in the possible dietary prevention of different diseases. Flavanones, stilbenes, lignans, isoflavonoids, and other flavonoid derivatives are similar in structure and provide host-protective purposes. They share the common parent compound, estrogen, in their synthesis and are differentiated based on key structural differences, specific plant hosts, and the environment (Fig. 1.7).
1.3 SOURCES
In 1936, Professor Szent-Györgyi reported the isolation of a substance that was a strong reducing agent acting as a cofactor in the reaction between peroxidase and ascorbic acid. This substance was initially given the name “vitamin P”; this substance has been subsequently categorized as the flavonoid rutin. Professor Szent-Györgyi’s seminal investigations identified rutin and reported its isolation from both lemons and red pepper.35 Since this time, more than other 4000 flavonoids have being identified and studied. Flavonoids are a group of polyphenolic compounds of low MW36 that present a common benzo-γ-pyrone structure.37 They are categorized into various subclasses including flavones, flavonols, flavanones, isoflavanones, anthocyanidins, and catechins.
Consumption of polyphenols could be close to 1 g/day in our diet, making polyphenols the largest source of antioxidants.38 Dietary sources of polyphenols include fruits, vegetables, cereals, legumes, chocolate, and plant-based beverages such as juices, tea, and wine.38 Extensive biomedical evidence suggests that polyphenolic compounds no matter their class may contribute to the prevention of cardiovascular disease, cancer, osteoporosis, diabetes, and neurodegenerative diseases.39–41 As polyphenols are found in plant sources consumed regularly or that are used in traditional medicine, there is a necessity to study these potentially beneficial compounds. Additionally, potential health benefiting properties such as antiinflammatory, antiproliferative, and colon protection may call for development of these compounds into future therapeutic agents. The average human diet contains a considerable amount of flavonoids, the major dietary sources of which include fruits (i.e., orange, grapefruit, apple, and strawberry), vegetables (i.e., onion, broccoli, green pepper, and tomato), soybeans, and a variety of herbs.42,43 Due to the constant and significant intake of these compounds in our diet, the United States Department of Agriculture (USDA) has created a database that contains the reported average content of these compounds in different foodstuffs.44 Among the classes of flavonoids, flavanones have been defined as citrus flavonoids44–46 due to their almost unique presence in citrus fruits.44,47–57 However, flavanones have been also reported in tomatoes,35,58–60 peanuts,61,62 and some herbs such as mint,63 gaviota tarplant,62,64 yerba santa,62,65 and thyme.62,66 Flavonoids are consumed in the human diet; the calculated flavonoid intake varies among countries since cultural dietary habits, available flora, and weather influence what food is consumed and, therefore, the amount and subclasses of flavonoids ingested.21 However, in the Western diet, the overall amount of flavonoids consumed on a daily basis is likely in the milligram range. It has been determined that the consumption of selected subclasses of flavonoids may be more important in determining health benefits than the total flavonoid intake. The content of flavonoids is also potentially influenced by food processing and storage conditions, which can result in transformation of flavonoids, and loss of flavonoid content.21
Flavonoids in general have been studied for more than 70 years in in vivo and in vitro systems. They have been shown to exert potent antioxidant activity 48,59,67–69 in some instances, stronger than α-tocopherol (vitamin E).70 They have been also shown to exhibit beneficial effects on capillary permeability and fragility,23,37,48,68,71–77 to have antiplatelet,23,37,48,67,68,71–76 hypolipidemic,67,78–81 antihypertensive,51,67,82 antimicrobial,67 antiviral,23,37,48,67,68,71–76,83,84 antiallergenic,85 antiulcerogenic,67 cytotoxic,67 antineoplastic,47,50,67,86–90 antiinflammatory,23,37,48,67,68,71–76 antiatherogenic,67,91 and antihepatotoxic67 activities. There are multiple chiral flavanones; however, they have been generally thought of as achiral entities and their chiral nature, in many cases, has not been recognized or denoted. Furthermore, the USDA database reports these compounds as achiral entities and uses the aglycone terminology interchangeably with the glycosides.92
The importance of considering the chiral nature of naturally occurring compounds and xenobiotics has been previously reviewed by Yáñez et al.93 The chirality of flavonoids was initially examined by Krause and Galensa’s studies in the early 1980s.62,94,95 Chirality plays an important role in biological activity; disciplines like agriculture, nutrition, and pharmaceutical sciences have long recognized the existence of natural chiral compounds; however, developed methods of analysis have often failed to stereospecifically separate and discriminate compounds into their respective antipodes. The advantage of chiral separation methods includes a more thorough appreciation of the stereospecific disposition of natural compounds including flavonoids. Moreover, the lack of configurational stability is a common issue with chiral xenobiotics. Some chiral flavonoids have been reported to undergo nonenzymatic interconversion of one stereoisomer into another in isomerization processes such as racemization and enantiomerization.93 Racemization refers to the conversion of an enantioenriched substance into a mixture of enantiomers. Alternatively, enantiomerization refers to a reversible interconversion of enantiomers. The importance of isomerization in stereospecific chromatography as well as in the pharmaceutical manufacturing process has been described.93 Therefore, the development of chiral methodology to analyze this kind of xenobiotics is necessary.
The study of the stereochemistry of flavonoids comprises mainly C-2 and C-3; nevertheless, the majority of natural flavonoids possess only one stereochemical isomer at the C-2 position. C-2 and C-3 act as chiral centers of dihydroxyflavonols and are important in flavonoid metabolism. The nomenclature of flavonoids with two chiral centers remains a topic of debate since the use of symbolism (+/−) or 2,3-cis or -trans seems to be inadequate to describe four possible enantiomers.96 It is also argued that the R, S nomenclature for absolute configuration is confusing for flavonoids because the designation of R or S changes at C-2 depending on the priority of neighboring groups, even though the stereochemistry remains the same.96 An alternative nomenclature system was proposed by Hemingway et al.97 based on that used for carbohydrate chemistry. In this system, the prefix ent- has been used for the mirror images. However, scientific consensus has not been reached on stereochemical lexicon cognates, and, to date, all these systems of nomenclature still remain being used and appearing in the biomedical, biochemical, agricultural, and food science literature.
1.4 PHARMACOLOGICAL ACTIVITIES OF SELECTED FLAVONOIDS
Humans have utilized and/or consumed polyphenols for health benefits. For centuries, alternative medicine has been practiced in different countries as exemplified by the use of plant extracts as traditional medicinal folk agents in the prevention and treatment of an assortment of ailments like menses, coughing, digestive problems, and so on. There are a variety of health benefits that can be attributed to the use/consumption of polyphenols including antioxidant, anticancer, antihyperlipidemic, antiallergenic, antibacterial, antiviral, and antiinflammatory.25 Conversely, there are also toxic effects associated with the use/consumption of polyphenols such as anemia due to the inhibited absorption of nutrients and minerals and inhibitory effects on cytochrome P450 enzymes (P450) resulting in potential drug–drug interactions. Current uses of polyphenols, in addition to their dietary health-related benefits and herbal remedies, are their use as dietary supplements and as pharmaceutical leads; thus, the reported intake of polyphenols is in the tens to hundreds of milligrams per day in human diets.21,31
The World Health Organization (WHO), published a comprehensive study and analysis in September 2008 naming the leading causes of mortality in the world in 2004 to include cardiovascular and pulmonary ailments and cancer accounting for approximately 22.9 million deaths.98 These statistics remain consistent with the data published in 2007 with similar primary causes of mortality as seen in 2002.99 There appears to be evidence that suggests that the leading causes of death are often multifactorial and intertwined, for example, dyspnea, malignant pericardial effusion, malignant pleural effusion, and superior vena cava syndrome, all of which are cardiopulmonary and/or vascular problems.100 Biomedical literature suggests etiologies of cardiovascular and pulmonary ailments and cancer have been linked to diet and nutrition, environment, exercise, genetics, hormones, lifestyles, radiation, sex, and weight; however, direct correlations of the disease, etiologies, and pathogenic mechanisms have not been fully elucidated. Contemporary Western medicine provides a variety of options to prevent and treat cardiovascular and pulmonary ailments and cancer. It is becoming increasingly popular and apparent that there is a need for other effective means to prevent, treat, and develop newer drugs or alternatives to disease treatment for both the consumer and the nutraceutical and pharmaceutical industry at a lower cost.
There are a several assay methodologies to determine the total polyphenolic content of a sample through the use of the Folin–Denis and Folin–Ciocalteu reagents and complexation with aluminum III ion.101–103 The Folin–Denis or Folin–Ciocalteu reducing reagents are able to form phosphomolybdic–phosphotungstic–phenol complexes, which can be monitored at a visible wavelength of 760 nm via reduction–oxidation reaction. These assays may have some inherent falsely elevated values because of interference as there may be other components in the sample that are also reducing reagents. As previously mentioned, the total phenolic content of the sample can be quantified; thus, this method is a nonspecific measurement of polyphenol content. Alternatively, complexation of polyphenols with aluminum III ion can be used to determine the quantity of polyphenols in the sample monitored at a wavelength of 425 nm. This method is dependent upon the aluminum ion complexing with the carbonyl and hydroxyl groups of the polyphenol. Again, these processes are not specific for a particular polyphenol; therefore, it is necessary to develop analytical methods to quantify individual polyphenols in a sample to enable determination of a correlation between the amount of a polyphenol in a sample and a health-related benefit.
1.4.1 Hesperidin and Hesperetin
Hesperidin ((+/−) 3,5,7-trihydroxy-4′-methoxyflavanone 7-rhamnoglucoside) C28H34O15, MW 610.56 g/mol, experimental octanol to water partition coefficient (XLogP) value of −1.1 (Fig. 1.8), is a chiral flavanone-7-O-glycoside consumed in oranges and in other citrus fruits and herbal products.104 The rutinose sugar moiety is rapidly cleaved off the parent compound to leave the aglycone bioflavonoid hesperetin (+/−3,5,7-trihydroxy-4′-methoxyflavanone) C16H14O6, MW 302.28 g/mol, XLogP value of 2.174 (Fig. 1.9), also a chiral flavonoid. There is current interest in the medical use of bioflavonoids, including hesperetin, in the treatment of a variety of cancers and vascular diseases.105
1.4.1.1 Antifungal, Antibacterial, and Antiviral Activity
Hesperidin extracted from grapefruit (Citrus paradise Macf., Rutaceae) seed and pulp ethanolic extracts has been related to have antibacterial and antifungal activity against 20 bacterial and 10 yeast strains.106 The level of antimicrobial effects was assessed employing an in vitro agar assay and standard broth dilution susceptibility test. It was observed that hesperidin exhibits strong antimicrobial activity against Salmonella enteritidis (minimum inhibitory concentration [MIC] of 2.06% extract concentration—m/V), while its activity against other bacteria and yeasts ranged from 4.13% to 16.5% m/V.106 Furthermore, hesperidin has also been observed to have protective effects in infected mice with encephalomyocarditis (EMC) virus and Staphylococcus aureus that were administered with hesperidin before or coadministered with the lethal viral-bacterial dose.107
In the case of the aglycone hesperetin, it has been shown to have MIC > 20 µg/mL against Helicobacter pylori. However, neither hesperetin nor other flavonoids and phenolic acids inhibited the urease activity of H. pylori.108 Furthermore, hesperetin has shown to be an effective in vitro agent against severe acute respiratory syndrome (SARS) (or similar) coronavirus (CoV) infections.109 Hesperetin inhibits the SARS-CoV replication by interacting with the spike (S) glycoprotein (S1 domain) in the host cell receptor and fusing the S2 domain with the host cell membrane activating the replicase polyproteins by the virus-encoded proteases (3C-like cysteine protease [3CLpro] and papain-like cysteine protease) and other virus-encoded enzymes such as the NTPase/helicase and RNA-dependent RNA polymerase. The blocking of the S1 may play an important role in the immunoprophylaxis of SARS.109 Similar activities have also been observed for hesperetin against the replication of the neurovirulent Sindbis strain (NSV) having 50% inhibitory doses (ID50) of 20.5 µg/mL. However, its glycoside, hesperidin, did not have inhibitory activity, indicating the possibility that the rutinose moiety of flavanones blocks the antiviral effect.110 Nevertheless, hesperetin has also been reported to be effective against the replication of herpes simplex virus type 1 (HSV-1), poliovirus type 1, parainfluenza virus type 3 (Pf-3), and respiratory syncytial virus (RSV) in in vitro cell culture monolayers employing the technique of viral plaque reduction.83
1.4.1.2 Antiinflammatory Activity
The inflammatory process involves a series of events encompassed by numerous stimuli such as infectious agents, ischemia, antigen–antibody interactions, and chemical, thermal, or mechanical injury. The inflammatory responses have been characterized to occur in three distinct phases, each apparently mediated by different mechanisms: an acute phase characterized by local vasodilatation and increased capillary permeability, a subacute phase characterized by infiltration of leukocyte and phagocyte cells, and a chronic proliferative phase, in which tissue degeneration and fibrosis occur.111 Different animal models have been developed to study the different phases of an inflammatory response. In the case of testing acute inflammatory response, the carrageenan-induced paw edema in mice112 and the xylene-induced ear edema113 are widely employed. Methods to test the proliferative phase (granuloma formation) include the cotton pellet granuloma model.114 Another model that allows the assessment of acute and chronic inflammation is the adjuvant–carrageenan-induced inflammation (ACII) model to induce adjuvant arthritis.115 Hesperidin and hesperetin were tested under these models, and it was observed that only hesperetin had a positive effect in reducing the carrageenan-induced paw edema in mice by 48% and 29% after 3 and 7 hours postinflammatory insult.111 In the case of the xylene-induced ear edema model, both hesperidin and hesperetin had a positive effect by reducing the edema by 45% and 44%, respectively.111 Similar observations were observed in the cotton pellet granuloma, whereas hesperidin and hesperetin inhibited granuloma formation by 30% and 28%, respectively.111 In the case of the ACII model, hesperidin exhibited activity in the acute phase (day 6) by causing a reduction in paw edema of 52% and exhibited a more moderate reduction in the chronic phase (7–21 days) by reducing the paw edema by 36%, 44%, 47%, 38%, and 31% at 7, 8, 10, 12, and 16 days postinflammatory insult, respectively.111 Different mechanisms to elucidate how hesperidin, hesperetin, and other polyphenols might carry their antiinflammatory activity have been proposed. Among these, it has been observed that after carrageenan injection, there is an initial release of histamine and serotonin during the first 1.5 hours with a posterior release of kinin between 1.5 and 2.5 hours, followed with a release of prostaglandins until 5 hours.116–118 Thus, it is believed that hesperidin and hesperetin might be involved with a variety of steps during the development of inflammation.
Other studies have reported that hesperidin downregulates the lipopolysaccharide (LPS)-induced expression of different proinflammatory (tumor necrosis factor-alpha [TNF-α], IL-1 beta, interleukin-6 [IL-6]) and antiinflammatory mediators (IL-12), cytokines as well as cytokines (KC, MCP-1 and MIP-2), while enhancing the production of other antiinflammatory cytokines (IL-4 and IL-10).119 In this study, mice were challenged with intratracheal LPS (100 µg) 30 minutes before treatment with hesperidin (200 mg/kg oral administration) or vehicle. After 4 and 24 hours, bronchoalveolar lavage fluid was collected, observing that hesperidin significantly reduced the total leukocyte counts, nitric oxide production, and inducible nitric oxide synthase (iNOS) expression.119 These results correlate with in vitro studies that have demonstrated that hesperidin suppresses the expression of IL-8 on A549 cells and THP-1 cells, the expression of TNF-α, IL-1 beta, and IL-6 on THP-1 cells, and the expression of intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) (responsible for cell adhesion) on A549 cells. The suppression of these inflammatory mediators is regulated by nuclear factor-kappa B (NF-κB) and AP-1, which are activated by IκB and mitogen-activated protein kinase (MAPK) pathways, indicating that hesperidin might interact within these pathways to exert its antiinflammatory activity.119
1.4.1.3 Antioxidant Activity
Hesperidin and its aglycone, hesperetin, have been assessed in various in vitro chemical antioxidant models (cell-free bioassay systems). It has been observed that both hesperidin and hesperetin exhibited similar patterns of 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activities.120 Similar results have been reported elsewhere for hesperidin, an antioxidant that was comparable in efficacy to Trolox® (positive control).121 Furthermore, hesperetin alone has been reported to effectively scavenge peroxynitrite (ONOO−) in a concentration-dependent manner. Peroxynitrite (ONOO−) is a reactive oxidant formed from superoxide (*O2−) and nitric oxide (*NO), which can oxidize several cellular components, including essential protein, nonprotein thiols, DNA, low density lipoproteins (LDLs), and membrane phospholipids.122
Both hesperidin and hesperetin have also been assessed for their antioxidant capacity in vivoin vivo12312412512641272+22120