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Dietary Interventions in Liver Disease: Foods, Nutrients, and Dietary Supplements [Pehme köide]

Edited by (Professor, Department of Clinical Biochemistry, Kings College Hospital, London), Edited by (Professor, Mel and Enid Zuckerman College of Public Health and School of Medicine, Arizona Health Sciences Center, University of Arizona, Tucson, AZ, USA)
  • Formaat: Paperback / softback, 428 pages, kõrgus x laius: 276x216 mm, kaal: 1180 g
  • Ilmumisaeg: 16-Jan-2019
  • Kirjastus: Academic Press Inc
  • ISBN-10: 0128144661
  • ISBN-13: 9780128144664
Teised raamatud teemal:
  • Formaat: Paperback / softback, 428 pages, kõrgus x laius: 276x216 mm, kaal: 1180 g
  • Ilmumisaeg: 16-Jan-2019
  • Kirjastus: Academic Press Inc
  • ISBN-10: 0128144661
  • ISBN-13: 9780128144664
Teised raamatud teemal:

Dietary Interventions in Liver Disease: Foods, Nutrients, and Dietary Supplements provides valuable insights into the agents that affect metabolism and other health-related conditions in the liver. It provides nutritional treatment options for those suffering from liver disease. Information is presented on a variety of foods, including herbs, fruits, soy and olive oil, thus illustrating that variations in intake can change antioxidant and disease preventing non-nutrients that affect liver health and/or disease promotion. This book is a valuable resource for biomedical researchers who focus on identifying the causes of liver diseases and food scientists targeting health-related product development.

  • Provides information on agents that affect metabolism and other health-related conditions in the liver
  • Explores the impact of composition, including differences based on country of origin and processing techniques
  • Addresses the most positive results from dietary interventions using bioactive foods to impact liver disease, including reduction of inflammation and improved function
List of Contributors
xv
Acknowledgments xix
Section I Overview of Liver Health
1 Genome-Based Nutrition in Chronic Liver Disease
Sonia Roman
Ingrid Rivera-Iniguez
Claudia Ojeda-Granados
Maricruz Sepulveda-Villegas
Arturo Panduro
1 Introduction
3(1)
1.1 Chronic Liver Disease
3(1)
1.2 Hepatopathogenic Diet and Its Variations by Liver Disease Etiology
3(1)
2 Genome-Based Nutrition: A Regionalized and Personalized Diet
4(1)
3 Genes, Microbiota, and Regionalized Diet
5(1)
4 Nutritional Intervention in Chronic Liver Disease
5(6)
4.1 Nonalcoholic Fatty Liver Disease---Nonalcoholic Steatohepatitis
6(2)
4.2 Alcoholic Liver Disease
8(1)
4.3 Hepatitis C Virus Infection
9(2)
5 Concluding Remarks
11(4)
List of Abbreviations
11(1)
Glossary
12(1)
References
12(3)
2 Current Therapeutic Strategies for Alcoholic Liver Disease
Alaa El-Din El-Sayed El-Sisi
Samia Salim Sokar
Dina Zakaria Mohamed
1 Introduction
15(1)
2 Pathogenesis of Alcoholic Liver Disease
16(1)
2.1 Alcoholic Fatty Liver (Steatosis)
16(1)
2.2 Alcoholic Hepatitis
16(1)
2.3 Alcoholic Fibrosis
16(1)
2.4 Alcoholic Cirrhosis
17(1)
3 Current Therapies for Alcoholic Liver Disease
17(14)
3.1 Abstinence and Lifestyle Modification
17(1)
3.2 Nutritional Support and Supplements
17(1)
3.3 Pharmacological Drugs and New Agents That Are Under Development
17(3)
3.4 Liver Transplantation
20(1)
3.5 Natural and Herbal Medicines for the Prevention and Treatment of ALD
20(1)
3.6 Herbal Formulas for Treatment of Alcoholic Liver Disease
20(5)
3.7 The Combination Therapies of Drugs and Natural Agents
25(1)
Endnotes
25(1)
References
25(6)
3 Features of Hepatic Encephalopathy
Mohamed M. Amin
1 Introduction
31(1)
2 Pathogenesis
31(1)
2.1 Ammonia Assumption
31(1)
2.2 Gamma-Aminobutyric Corrosive Assumption
32(1)
2.3 Changeability of Hepatic Encephalopathy
32(1)
3 Clinical Features of Hepatic Encephalopathy
32(1)
4 Laboratory Irregularities in Hepatic Encephalopathy
33(1)
5 Regular Precipitants of Hepatic Encephalopathy
33(1)
6 Distinguishable Diagnosis for Hepatic Encephalopathy
34(1)
7 Controlling of Hepatic Encephalopathy
34(3)
7.1 Methodology Respects
34(1)
7.2 Medications to Decrease Intestinal Ammonia Production
34(2)
7.3 Measurements to Upregulate Ammonia Clearance
36(1)
7.4 Medicines to Improve Sleep Disturbances
37(1)
7.5 Post-Transjugular Intrahepatic Portosystemic Shunt Hepatic Encephalopathy
37(1)
8 Insignificant Hepatic Encephalopathy
37(2)
References
37(2)
4 The Liver Before and After Bariatric Surgery
Flavio A. Cadegiani
1 Introduction: The Liver of the Obese Patient
39(6)
1.1 Biochemical Markers and Alterations of the Liver in Obesity
39(3)
1.2 Gene Expressions and Polymorphisms in the Sick Liver of the Obese
42(1)
1.3 The Challenging Management of NAFLD, NASH, Liver Fibrosis, and Cirrhosis in Obesity
42(1)
1.4 Preparation for Bariatric Surgery in the Patient With Liver Dysfunction
42(3)
2 The Liver After the Bariatric Surgery
45(7)
2.1 Methods of Analysis of the Liver (Before and) After Bariatric Surgery
47(1)
2.2 Biochemical Markers of the Liver After Bariatric Surgery
47(2)
2.3 Genes Expression After Bariatric Surgery
49(1)
2.4 Liver Transplantation and Bariatric Surgery
50(2)
2.5 Liver Complications After Bariatric Surgery
52(1)
2.6 Weight-Loss-Independent Effects of Bariatric Surgery
52(1)
3 Final Discussion
52(1)
4 Conclusion
53(6)
References
53(6)
5 Oxidative Stress and Dysfunction of the Intracellular Proteolytic Machinery: A Pathological Hallmark of Nonalcoholic Fatty Liver Disease
Takujiro Homma
Junichi Fujii
1 Introduction
59(1)
2 Intracellular Proteolysis
59(2)
2.1 The Ubiquitin-Proteasome System
59(1)
2.2 Autophagy
60(1)
2.3 Crosstalk Between the UPS and Autophagy
60(1)
3 ROS and Intracellular Proteolysis
61(2)
3.1 Inhibition of UPS by ROS
61(1)
3.2 Inhibition of Autophagy by ROS
61(2)
4 The Interconnection of ROS, Intracellular Proteolysis, and NAFLD
63(3)
4.1 Nonalcoholic Fatty Liver Disease
63(1)
4.2 Oxidative Stress and NAFLD
63(1)
4.3 Impaired Intracellular Proteolysis in NAFLD
63(1)
4.4 Multiple Mechanisms of Autophagic Dysfunction in NAFLD
64(1)
4.5 Upregulation of Rubicon in NAFLD
65(1)
5 Conclusion Remarks
66(7)
References
66(7)
Section II Fruits Improve Liver Health
6 Polyphenols in the Management of Chronic Liver Diseases Including Hepatocellular Carcinoma
Surendra Kumar Shukla
Vijay Kumar
1 Introduction
73(1)
2 Dietary Polyphenols in the Prevention of Chronic Liver Diseases
73(1)
3 Effect on Non-alcoholic Fatty Liver Diseases
74(1)
4 Effect on Nonalcoholic Steatohepatitis
75(1)
5 Effect of Polyphenols on Alcoholic Liver Diseases
75(1)
6 Control of Hepatitis B Virus Infection
75(1)
7 Control of Hepatitis C Virus Infection
76(1)
8 Management of Hepatocellular Carcinoma
76(1)
9 Conclusions
76(3)
List of Abbreviations
76(1)
Glossary
77(1)
References
77(2)
7 Phytochemicals in the Prevention of Ethanol-Induced Hepatotoxicity: A Revisit
Manjeshwar Shrinath Baliga
Arnadi Ramachandrayya Shivashankara
Sunitha Venkatesh
Harshith P. Bhat
Princy Louis Palatty
Ganesh Bhandari
Suresh Rao
1 Introduction
79(1)
2 Phytochemicals in the Protection of Alcohol-Induced Hepatotoxicity
79(7)
2.1 Beta-Carotene
79(1)
2.2 Lutein
80(1)
2.3 Meso-Zeaxanthin
81(1)
2.4 Betaine
81(1)
2.5 Ferulic Acid
82(1)
2.6 Ellagic Acid
83(1)
2.7 Epigallocatechin-3-Gallate
83(1)
2.8 Quercetin
84(1)
2.9 Morin
84(1)
2.10 Hydroxystilbenes and Resveratrol
84(1)
2.11 Ursolic Acid
85(1)
2.12 Andrographolide and Arabinogalactan Proteins of Andrographis paniculata Nees
85(1)
2.13 Picroliv
85(1)
2.14 Silymarin
85(1)
3 Mechanisms
86(1)
4 Conclusions
86(5)
List of Abbreviations
86(5)
References
87(4)
8 Protective Actions of Polyphenols in the Development of Nonalcoholic Fatty Liver Disease
Yoojin Lee
Ji-Young Lee
1 Introduction
91(1)
2 Pathogenesis and Progression of NAFLD
91(2)
2.1 Liver Steatosis
91(1)
2.2 Hepatic Oxidative Stress, Inflammation, and Apoptosis
92(1)
2.3 Liver Fibrosis
93(1)
3 Polyphenols in Foods and Natural Products
93(1)
4 Protective Action of Polyphenols Against NAFLD Progression
94(2)
4.1 Quercetin
94(1)
4.2 Epigallocatechin-3-O-Gallate
94(1)
4.3 Anthocyanins
95(1)
4.4 Resveratrol
95(1)
5 Conclusion
96(5)
References
96(5)
9 Phytotherapy for the Liver
Erika Ramos-Tovar
Pablo Muriel
1 Introduction
101(1)
2 Liver Disease Treatment
101(1)
3 Plant-Derived Compounds With Liver Beneficial Properties
101(1)
4 Curcuma Ionga
102(1)
4.1 Antiinflammatory Properties
102(1)
4.2 Antifibrotic Properties
102(1)
4.3 Anticancer Properties of Curcumin
103(1)
4.4 Anti heavy Metal Properties of Curcumin in the Liver
103(1)
4.5 Antisteatotic Properties of Curcumin
103(1)
5 Silybum marianum
103(2)
5.1 Antiinflammatory and Immunomodulation Activities
104(1)
5.2 Silymarin Prevents Fibrosis
104(1)
5.3 Beneficial Effects of Silymarin on NAFLD
104(1)
5.4 Anticancer Properties of Silymarin
104(1)
6 Quercetin
105(1)
6.1 Quercetin Inhibits Liver Inflammation
105(1)
6.2 Quercetin and Hepatic Fibrosis
105(1)
6.3 Quercetin and Nonalcoholic Steatohepatitis
106(1)
6.4 Quercetin and Hepatocellular Carcinoma
106(1)
7 Naringenin
106(1)
7.1 Antiinflammatory Properties of Naringenin
106(1)
7.2 Naringenin Antifibrogenic Effects
107(1)
7.3 Naringenin and Hepatocellular Carcinoma
107(1)
8 Coffee
107(1)
9 Stevia
108(1)
10 Resveratrol
108(1)
11 L-Theanine
108(1)
12 Hesperidin
109(1)
13 Colchicine
109(1)
14 Rosemary
109(1)
15 Glycyrrhizin (Glycyrrhizic Acid)
109(1)
16 Other Plant-Derived Compounds
110(1)
17 Conclusions and Perspectives
110(15)
Acknowledgments
114(1)
References
114(11)
Section III Herbs and Plants for Treating Liver Disease
10 Curcuma Ionga, the Polyphenolic Curcumin Compound and Pharmacological Effects on Liver
Bui Thanh Tung
Dong Thi Nham
Nguyen Thanh Hai
Dang Kim Thu
1 Introduction of Curcuma Ionga
125(2)
1.1 Chemical Composition in the Rhizome of Curcuma Ionga L.
125(2)
2 The Polyphenolic Curcumin Compound
127(4)
2.1 The Therapeutic Potential of Curcuma Ionga Components
127(1)
2.2 Antibacterial Activity
127(1)
2.3 Antioxidant Activity
127(1)
2.4 Anti-inflammatory Activity
128(1)
2.5 For Treatment of Arthritis
128(1)
2.6 For Treatment of Metabolic Syndrome
129(1)
2.7 For Treatment of Cancer
130(1)
3 Curcumin and Liver Disease
131(1)
3.1 Curcumin Against Heavy Metals-Induced Liver Damage
131(1)
3.2 The Effects of Curcumin in Preclinical In Vitro and In Vivo HCC
131(1)
3.3 Hepatitis B Virus
132(1)
4 Conclusions
132(3)
List of Abbreviations
132(3)
References
133(2)
11 Nymphaea alba and Liver Protection
Riham O. Bakr
1 Introduction
135(1)
2 Traditional Uses
135(1)
3 Phytoconstituents
136(1)
3.1 Flower Phytoconstituents
136(1)
3.2 Leaf Phytoconstituents
136(1)
3.3 Rhizome Phytoconstituents
137(1)
4 Validated Studies
137(3)
4.1 Hepatoprotective Effect of Flowers and a Powerful Anti-Inflammatory Activity
138(1)
4.2 Leaf Extract and Potent Biological Activities
139(1)
4.3 Rhizomes' Biological Activities
139(1)
5 Phenolics of N. alba and Liver Protection
140(1)
6 Conclusion
141(4)
List of Abbreviations
141(4)
References
142(3)
12 The Flavone Baicalein and Its Use in Gastrointestinal Disease
Yangchun Xie
Rui Kang
Daolin Tang
1 Introduction
145(1)
2 Extraction and Purification
145(1)
3 Metabolism and Conversion
145(1)
4 Use of Baicalein in Gastrointestinal Disease
146(2)
4.1 Ulcerative Colitis
146(1)
4.2 Gastric Ulceration
146(1)
4.3 Ischemia-Reperfusion Injury
146(1)
4.4 Liver Fibrosis
147(1)
4.5 Cancer Prevention and Therapy
147(1)
4.6 Colorectal Cancer
147(1)
4.7 Pancreatic Cancer
147(1)
4.8 Gastric Cancer
147(1)
4.9 Hepatocellular Carcinoma
148(1)
4.10 Diabetes Mellitus
148(1)
5 Mechanism of Action of Baicalein
148(3)
5.1 Regulation of Cell Death
148(1)
5.2 Regulation of Signaling Transduction
149(2)
6 Conclusion
151(6)
Acknowledgments
151(1)
References
151(6)
13 Pyrroloquinoline Quinone: Its Profile, Effects on the Liver and Implications for Health and Disease Prevention
Karen R. Jonscher
Robert B. Rucker
1 Introduction: Pyrroloquinoline Quinone
157(4)
2 Factors Contributing to the Development of NAFLD/NASH
161(1)
3 Systemic Effects of PQQ on NAFLD/NASH
162(5)
3.1 Mechanistic Modes of Action
162(1)
3.2 Pyrroloquinoline Quinone as an Antioxidant
162(1)
3.3 Pyrroloquinoline Quinone and Lipid Metabolism
162(3)
3.4 Pyrroloquinoline Quinone and Inflammation
165(1)
3.5 Pyrroloquinoline Quinone and the Microbiome
165(1)
3.6 Pyrroloquinoline Quinone and Fibrosis
166(1)
4 Human Studies and Implications for Health
167(1)
4.1 Pyrroloquinoline Quinone and Cognition
167(1)
4.2 Pyrroloquinoline Quinone and Skin Elasticity
167(1)
4.3 Pyrroloquinoline Quinone and Metabolism
168(1)
5 Conclusions
168(7)
References
168(7)
14 Herbal Weight Loss Supplements: From Dubious Efficacy to Direct Toxicity
Armando E. Gonzalez-Stuart
Jose O. Rivera
1 Introduction
175(1)
2 The Surge of Herbal Product Use Within Complementary and Alternative Medicine
175(1)
3 The Internet as a Source of Information About Herbal Weight Loss Supplements
176(1)
4 Herbal Supplement Identity, Efficacy, and Safety: Bedlam in the Cyber Marketplace
176(1)
5 Mexican Hawthorn Root
176(1)
5.1 Yellow Oleander or "Codo de Fraile"
177(1)
6 Toxicity of Thevetia spp.
177(1)
7 Candlenut Tree Seed
178(1)
8 Botanical Characteristics
178(1)
9 Use of the Candlenut Tree in Asian Traditional Medicine
178(1)
10 Weight Loss and Other Health Claims Made on the Internet for Candlenut Tree Seeds
179(1)
11 International Health Agencies Ban Candlenut Seed Due to Its Toxicity
179(1)
12 Conclusions
179(4)
References
180(3)
15 Tea (Camellia sinensis L. Kuntze) as Hepatoprotective Agent: A Revisit
Arnadi Ramachandrayya Shivashankara
Suresh Rao
Thomas George
Soniya Abraham
Marshal David Colin
Princy Louis Palatty
Manjeshwar Shrinath Baliga
1 Introduction
183(1)
2 Phytochemistry of Tea
183(1)
3 Validated Uses
183(1)
4 Tea Protects Against the Alcohol-Induced Hepatotoxicity
184(1)
5 Tea Protects Against Carbon Tetrachloride-lnduced Hepatotoxicity
185(1)
6 Effect of Tea on N-Acetaminophen-Induced Hepatotoxicity
186(1)
7 Tea Is Effective in Viral Hepatitis
186(1)
8 Effect of Tea on Ischemia-Reperfusion Injury
186(1)
9 Effect of Tea on Fatty Liver Disease
186(1)
10 Effect of Tea on Hepatotoxicity of Lead
187(1)
11 Effect of Tea on Hepatotoxicity of Arsenic
187(1)
12 Effect of Tea on Phenobarbitol-Induced Liver Damage
187(1)
13 Effect of Tea on Hepatotoxicity of Microcystin
187(1)
14 Effect of Tea on Hepatotoxicity of Aflatoxins
187(1)
15 Effect of Tea on Hepatotoxicity of Azathioprine
188(1)
16 Effect of Tea on Galactosamine-and Lipopolysaccharide-Induced Liver Damage
188(1)
17 Effect of Tea on Hepatotoxicity of Insecticides
188(1)
18 Effect of Tea on Hepatocarcinogenesis
188(1)
19 Conclusions
189(4)
List of Abbreviations
190(1)
References
190(3)
16 Hepatoprotective Effects of the Indian Gooseberry (Emblica officinalis Gaertn): A Revisit
Manjeshwar Shrinath Baliga
Arnadi Ramachandrayya Shivashankara
K.R. Thilakchand
M.P. Baliga-Rao
Princy Louis Palatty
Thomas George
Suresh Rao
1 Introduction
193(1)
2 Phytochemicals
193(1)
3 Traditional Uses
193(1)
4 Scientifically Validated Studies
194(1)
5 Effect of Amla on Hepatotoxicity of Ethanol
195(1)
6 Effect of Amla on Hepatotoxicity of Heavy Metals Arsenic and Cadmium
195(1)
7 Effect of Amla on Hepatotoxicity of Iron Overload
196(1)
8 Effect of Amla on Hepatotoxicity of Ochratoxin
196(1)
9 Effect of Amla on Hepatotoxicity of Antitubercular Drugs
196(1)
10 Effect of Amla on Hepatotoxicity of Hexachlorocyclohexane
196(1)
11 Effect of Amla on Hepatotoxicity of Carbon Tetrachloride
196(1)
12 Effect of Amla on Hepatotoxicity of Paracetamol
197(1)
13 Effect of Amla Phytochemicals on Galactosamine- and Lipopolysaccharide-Induced Liver Damage
197(1)
14 Effect of Amla Phytochemicals on Hepatotoxicity of Microcystin
197(1)
15 Effect of Amla on Hepatocarcinogenesis
197(1)
16 Effect of Amla on Hepatic Lipid Metabolism and Metabolic Syndrome
198(1)
17 Effect of Amla on Nonalcoholic Fatty Liver Disease
198(1)
18 Mechanism of Action(s) Responsible for the Hepatoprotective Effects
198(1)
19 Conclusions
199(6)
List of Abbreviations
199(1)
References
200(1)
Further Reading
201(4)
Section IV Dietary Macronutrients and Micronutrients for Healthy Liver Function
17 Major Dietary Interventions for the Management of Liver Disease
Idris Adewale Ahmed
1 Introduction
205(1)
2 Liver as an Organ
206(1)
3 Liver Failure
206(1)
4 Causes of Hepatic Injury
206(1)
5 Nonalcoholic Fatty Liver Disease
206(1)
6 Alcoholic Liver Disease
207(1)
7 Chronic Hepatitis B and Chronic Hepatitis C
207(1)
8 Hepatocellular Carcinoma
207(1)
9 Dietary Interventions in the Management of Liver Diseases
208(1)
10 Diet Types
208(1)
11 Fat
208(1)
12 Protein
208(1)
13 Carbohydrates
208(1)
14 Glycemic Index
209(1)
15 Antioxidants
209(1)
16 Bile Acids and Fiber
209(1)
17 Prebiotics and Probiotics
209(1)
18 The Mediterranean and Other Diets
210(1)
19 Zinc
210(1)
20 Niacin (Nicotinic Acid)
210(1)
21 Astaxanthin
210(1)
22 Curcumin
210(1)
23 Conclusion
210(3)
References
211(2)
18 The Effects of Dietary Advanced Glycation End Products (AGEs) on Liver Disorders
Fahimeh Agh
Farzad Shidfar
1 Advanced Glycation End Products
213(2)
2 Circulating AGEs and Liver Disorders
215(1)
3 The AGEs-RAGE System in Liver Disorders
216(2)
4 The Effects of Dietary AGEs on Liver Disorders
218(6)
4.1 Liver Histology
218(3)
4.2 Liver Enzymes
221(1)
4.3 Metabolic and Inflammatory Profiles
221(1)
4.4 Reactive Oxygen Species Production
222(1)
4.5 Receptor for Advanced Glycation End Products
223(1)
4.6 De Novo Lipogenesis
223(1)
4.7 Weight Gain
224(1)
5 Dietary Interventions to Reduce the AGEs
224(1)
6 Summary
224(9)
List of Abbreviations
227(1)
References
228(5)
19 Molecular Mechanisms of the Protective Role of Wheat Germ Oil Against Oxidative Stress---Induced Liver Disease
El-Sayed Akool
1 Introduction
233(1)
2 Reactive Oxygen Species and Liver Diseases
233(2)
3 Wheat Germ Oil and Liver Diseases
235(4)
3.1 Nutritional Composition
235(1)
3.2 Antioxidant Activity
235(1)
References
236(3)
20 Critical Role of Hepatic Fatty-Acyl Phospholipid Remodeling in Obese and Nonobese Fatty Liver Mouse Models
Walee Chamulitrat
Gerhard Liebisch
Anita Pathil
Wolfgang Stremmel
1 Introduction
239(2)
1.1 Causes of Obesity: Genetics and Diets
239(1)
1.2 Consequence of Obesity: NAFLD and NASH
239(1)
1.3 Animal Models of Obese and Nonobese NAFLD/NASH
240(1)
1.4 Comparison of Hepatic Lipids Among Obese and Nonobese NAFLD/NASH
241(1)
2 Phospholipids in NAFLD and NASH
241(3)
2.1 Linking Hepatic Triglyceride to Phospholipid in NAFLD
241(1)
2.2 Comparison of Hepatic Phospholipid Among Obese and Nonobese NAFLD/NASH
241(2)
2.3 Comparison of Hepatic Phospholipid Ratios Among Obese and Nonobese NAFLD/NASH
243(1)
3 Phospholipid-Metabolizing Genes in Obesity and NAFLD
244(3)
3.1 PLA2G6 or iPLA2β in Obesity and NAFLD
245(1)
3.2 Effects of iPLA2β Deficiency on Phospholipids in Obese Ob/Ob and HFD-Fed Mice
245(2)
3.3 Effects of iPLA2β Deficiency on Phospholipids in MCD-Fed Mice
247(1)
4 Summarized Findings and Proposed Mechanisms
247(4)
5 Perspectives
251(1)
5.1 Use of iPLA2β Antagonists for Steatosis Protection in Obese Versus Nonobese NAFLD
251(1)
5.2 Considerations and Precautions
252(1)
6 Conclusions
252(5)
List of Abbreviations
252(1)
Acknowledgments
253(1)
References
253(4)
21 Vitamin D3 and Liver Protection
Malath Azeez Al-Saadi
1 Introduction
257(1)
1.1 Mechanism of Action
257(1)
2 Materials and Methods
258(1)
2.1 Drugs
258(1)
2.2 Study Design
258(1)
2.3 Induction of Acute Hepatotoxicity
258(1)
2.4 Statistical Analysis
258(1)
3 Results
259(1)
4 Discussion
259(4)
References
260(3)
22 The Role of Carbohydrate Response Element-Binding Protein in the Development of Liver Diseases
Katsumi lizuka
1 Introduction
263(1)
2 ChREBP, a Glucose-Activated Transcription Factor That Regulates Glucose and Lipid Metabolism
263(1)
3 Dietary Composition and ChREBP
263(1)
4 ChREBP and Liver Diseases
264(4)
4.1 Nonalcoholic Fatty Liver Disease
264(1)
4.2 Alcoholic Liver Disease
265(2)
4.3 Liver Tumors
267(1)
4.4 Virus Infection
267(1)
4.5 Glycogen Storage Diseases
268(1)
5 Supplement and ChREBP
268(2)
5.1 Polyunsaturated Fatty Acids
268(1)
5.2 Ketone Bodies
269(1)
5.3 Vinegar (Acetic Acid)
269(1)
5.4 Polyphenols
269(1)
6 Conclusion
270(5)
Acknowledgments
270(1)
References
271(4)
23 Trans Fatty Acid in the Liver and Central Nervous System
Rafael Longhi
1 Introduction
275(1)
2 Hydrogenation Process
275(1)
3 Biochemical Metabolism
276(1)
4 Trans Fatty Acids and Liver Damage
276(4)
4.1 Cell Culture
276(1)
4.2 Animal Models
277(2)
4.3 Human Trials
279(1)
5 Trans Fatty Acids and the Central Nervous System
280(4)
5.1 Animal Studies
281(2)
5.2 Human Trials
283(1)
6 Final Considerations
284(3)
References
284(3)
24 Fish Oil Supplements During Perinatal Life: Impact on the Liver of Offspring
Emilio Herrera
Encarnacion Amusquivar
1 Introduction
287(1)
2 Role of Fatty Acids in Fetal Development
287(1)
3 Fatty Acids and Epigenetics
288(1)
4 Fish Oil Supplements During Pregnancy
288(2)
5 Prevalence and Pathogenic Aspects of Nonalcoholic Fatty Liver Disease
290(1)
6 Fetal Programming Origins of NAFLD
290(1)
7 Potential Protective Role of Fish Oil in the NAFLD Development
291(6)
Acknowledgments
292(1)
References
292(5)
25 Purple Rice Bran Improves Hepatic Insulin Signaling via Activation of Akt and Stabilization of IGF in Diabetic Rats
Ei Ei Hlaing
Supicha Rungcharoenarrichit
Narissara Lailerd
Sittiruk Roytrakul
Pichapat Piamrojanaphat
1 Introduction
297(1)
2 Methods
298(2)
2.1 Tissue Preparation and Homogenization
298(1)
2.2 Determination of Tissue Protein Concentration
298(1)
2.3 One-Dimensional SDS-PAGE Analysis
298(1)
2.4 In-Gel Tryptic Digestion Before LC-MS/MS Analysis
298(1)
2.5 Peptide Identification and Quantitation by LC-MS/MS Analysis
299(1)
2.6 Bioinformatics Analysis
299(1)
2.7 Confirmation of Candidate Genes and Their Affected Proteins
299(1)
2.8 mRNA Level of Affected Genes by Quantitative Real-Time PCR
300(1)
2.9 Affected Protein Expression Level by Western Blot Analysis
300(1)
2.10 Statistical Analysis
300(1)
3 Results
300(5)
3.1 LC-MS/MS Analysis and Hepatic Proteins Identification
300(1)
3.2 Functional Categories of Identified Hepatic Proteins of Diabetic Rats and Diabetic Rats With Purple Rice Bran Supplement
301(2)
3.3 Bioinformatic Analysis of Unique Proteins Found in the Hepatic Tissues of Diabetic Rats and Diabetic Rats With Purple Rice Bran Supplement
303(1)
3.4 mRNA Expression Level of Candidate Genes of Diabetic Rats' Liver
304(1)
3.5 mRNA Expression Level of Rangap1 Gene
304(1)
3.6 mRNA Expression Level of Candidate Genes of Purple Rice Bran-Supplemented Diabetic Rats' Liver
304(1)
3.7 mRNA Expression Level of Affected Genes From Hepatic Proteomic Analysis
304(1)
3.8 Protein Expression Level of Affected Proteins From Hepatic Proteomic Analysis
305(1)
4 Discussion and Conclusion
305(10)
Acknowledgments
312(1)
References
312(1)
Further Reading
312(3)
Section V Toxic Dietary Materials Including Alcohol-Induced Liver Dysfunction: Treatment
26 Heavy Metals and Low-Oxygen Microenvironment---Its Impact on Liver Metabolism and Dietary Supplementation
Kusal K. Das
Rajesh Honnutagi
Lata Mullur
R. Chandramouli Reddy
Swastika Das
Dewan Syed Abdul Majid
M.S. Biradar
1 Introduction
315(2)
2 Heavy Metals and Its Interactions
317(1)
2.1 Heavy Metal Toxicities: Nickel and Lead
317(1)
3 Hypoxia Pathophysiology
318(1)
3.1 Hypoxia Microenvironment
318(1)
3.2 Hypoxia and Heavy Metals (Nickel and Lead)
318(1)
4 Heavy Metals in Liver Diseases
319(2)
4.1 Heavy Metals and Liver Pathophysiology (Nickel and Lead)
319(2)
4.2 Possible Mechanism of Altered Hepatocellular Architecture by Heavy Metals
321(1)
5 Hypoxia and Liver Diseases
321(2)
5.1 Hypoxia---Liver Histopathology
322(1)
5.2 Hypoxia and Heavy Metals (Nickel and Lead)---Liver Histopathology
323(1)
6 Heavy Metals (Nickel and Lead), Hypoxia, and Liver Functions-Role of Dietary Supplementations
323(5)
6.1 Heavy Metals, Liver Functions, and Dietary Supplementation
324(1)
6.2 Hypoxia, Liver Function, and Dietary Supplementation
324(1)
6.3 Heavy Metals, Hypoxia, and Liver Functions---Dietary Supplementation
325(3)
7 Conclusion
328(5)
Acknowledgments
329(1)
References
329(4)
27 Cadmium and Fullerenes in Liver Diseases
Sinisa Djurasevic
Zoran Todorovic
Sladjan Pavlovic
Snezana Pejic
1 Introduction
333(2)
1.1 Cytochromes P450
333(1)
1.2 Xenobiotic Metabolism and Hepatotoxicity
334(1)
2 Liver and Oxidative Stress
335(1)
2.1 Oxidative Stress and Liver Disorders
335(1)
3 Cadmium as the Model of Hepatotoxicity
336(2)
3.1 Molecular Mechanisms of Cadmium Toxicity
337(1)
3.2 Cadmium and Oxidative Stress
337(1)
3.3 Cadmium and Liver Injury in Animals
338(1)
3.4 Cadmium and Mitochondria
338(1)
4 Fullerenes and Liver Protection
338(7)
4.1 Chemical Properties of Fullerenes
338(1)
4.2 Pharmacological Properties of Fullerenes
339(1)
4.3 Fullerenes as the Protectors in the Carbon Tetrachloride Model of Liver Toxicity
339(1)
Acknowledgments
340(1)
References
340(5)
28 Beneficial Effects of Natural Compounds on Heavy Metal-Induced Hepatotoxicity
Parisa Hasanein
Abbasali Emamjomeh
1 Introduction
345(1)
2 Arsenic Hepatotoxicity
346(1)
2.1 Mechanisms of Arsenic-Induced Hepatotoxicity
346(1)
3 Cadmium Hepatotoxicity
346(1)
3.1 Mechanisms of Cadmium-Induced Hepatotoxicity
347(1)
4 Chromium Hepatotoxicity
347(1)
4.1 Mechanisms of Chromium-Induced Hepatotoxicity
347(1)
5 Copper Hepatotoxicity
348(1)
5.1 Mechanisms of Copper-Induced Hepatotoxicity
348(1)
6 Lead Hepatotoxicity
348(1)
6.1 Mechanisms of Lead-Induced Hepatotoxicity
348(1)
7 Mercury Hepatotoxicity
349(1)
7.1 Mechanisms of Mercury-Induced Hepatotoxicity
349(1)
8 Effects of Natural Products on Heavy Metal-Induced Hepatotoxicity
350(7)
8.1 Vitamins C and E
350(1)
8.2 Curcumin
350(1)
8.3 N-Acetyl cysteine
350(1)
8.4 α-Lipoic Acid
351(1)
8.5 Melatonin
351(1)
8.6 Flavonoid-Rich Extracts
351(1)
8.7 Anthocyanidins
352(1)
8.8 Quercetin
352(1)
8.9 Naringenin
352(1)
8.10 Black Tea
352(1)
8.11 Olive Oil
352(1)
8.12 Sesame Oil
352(1)
8.13 Combination Therapy
352(1)
References
353(4)
29 Nutritional and Dietary Interventions for Nonalcoholic Fatty Liver Disease
Cindy X. Cai
Stella Carlos
Pejman Solaimani
Bansari J. Trivedi
Chuong Tran
Shobha Castelino-Prabhu
1 Introduction
357(1)
2 Epidemiology
357(1)
3 Risk Factors
357(1)
4 Pathogenesis
358(2)
5 Clinical Manifestations
360(1)
6 Histopathology
360(1)
7 Diagnosis
360(1)
8 Natural Course and Outcomes
361(1)
9 Treatment
361(5)
9.1 Lifestyle Modification for NAFLD
361(4)
9.2 Pharmacological Treatment
365(1)
9.3 Bariatric Surgery and Endoscopic Bariatric Intervention
366(1)
10 Conclusions
366(7)
References
367(6)
30 Dietary Management of Nonalcoholic Fatty Liver Disease (NAFLD) by n-3 Polyunsaturated Fatty Acid (PUFA) Supplementation: A Perspective on the Role of n-3 PUFA-Derived Lipid Mediators
S.M. Jeyakumar
A. Vajreswari
1 Background
373(1)
2 NAFLD-Worldwide Burden
373(1)
3 Dietary Carbohydrates: A Glance at Fructose
374(1)
4 Hepatic Fructose Metabolism
374(1)
5 Fructose, the Common Etiological Factor of NAFLD
374(2)
6 Management of NAFLD
376(1)
7 Pharmacotherapy
376(1)
8 Lifestyle Intervention
376(1)
9 Dietary Fat
376(2)
10 Metabolic Fate of n-3 Long-Chain PUFA: Bioactive Lipid Mediators
378(1)
11 Eicosapentaenoic Acid (EPA; C20:5n-3)--Derived Lipid Mediators
378(1)
12 Docosahexaenoic Acid (DHA; C22:6n-3)--Derived Lipid Mediators
378(1)
13 n-3 PUFA and NAFLD
379(3)
14 Lipid Mediators of n-3 PUFA and NAFLD
382(2)
15 Conclusion
384(7)
Acknowledgments
384(1)
References
384(7)
Index 391
Ronald Ross Watson, PhD, is Professor of Health Promotion Sciences at the University of Arizona, Mel and Enid Zuckerman College of Public Health. Dr. Watson began his research in public health at the Harvard School of Public Health as a Fellow in 1971 doing field work on vaccines in Saudi Arabia. He has done clinical studies in Colombia, Iran, Egypt, Saudi Arabia and the United States which provides a broad international view of public health. He has served in the military reserve hospital for 17 years with extensive training in medical responses to disasters as the chief biochemistry officer of a general hospital, retiring as a Lt. Colonel. He is a distinguished member of several national and international nutrition, immunology, and cancer societies. Dr. Watsons career has involved studying many lifestyle aspects for their uses in health promotion. He has edited over 100 biomedical reference books and 450 papers and chapters. His teaching and research focuses on alcohol, tobacco, and drugs of abuse in heart function and disease in mouse models. Victor R. Preedy BSc, PhD, DSc, FRSB, FRSPH, FRSC, FRCPath graduated with an Honours Degree in Biology and Physiology with Pharmacology. After gaining his University of London PhD, he received his Membership of the Royal College of Pathologists. He was later awarded his second doctorate (DSc), for his contribution to protein metabolism in health and disease. He is Professor of Clinical Biochemistry (Hon) at Kings College Hospital and Emeritus Professor of Nutritional Biochemistry at Kings College London. He has Honorary Professorships at the University of Hull, and the University of Suffolk. Professor Preedy was the Founding Director and then long-term Director of the Genomics Centre at Kings College London from 2006 to 2020. Professor Preedy has been awarded fellowships of the Royal Society of Biology, the Royal College of Pathologists, the Royal Society for the Promotion of Health, the Royal Institute of Public Health, the Royal Society for Public Health, the Royal Society of Chemistry and the Royal Society of Medicine. He carried out research when attached to the National Heart Hospital (part of Imperial College London), The School of Pharmacy (now part of University College London) and the MRC Centre at Northwick Park Hospital. He has collaborated with international research groups in Finland, Japan, Australia, USA, and Germany. To his credit, Professor Preedy has published over 750 articles, which includes peer-reviewed manuscripts based on original research, abstracts and symposium presentations, reviews and edited books.