Showing posts with label Multiple choice questions. Show all posts
Showing posts with label Multiple choice questions. Show all posts

Wednesday, 20 May 2020

Gupta's Series 18: Brain Storming Questions in Toxicology : MCQ's

Prof PK Gupta Toxicologist








Brain Storming Questions in Toxicology by Prof PK Gupta

First edition published 2020 by CRC Press 6000 Broken Sound Parkway NW, Suite 300,Boca Raton, FL 33487-2742

CONTENTS

Preface ix

Author xi

Section 1: General toxicology

Chapter 1 Principles of Toxicology 3
Chapter 2 Disposition and Toxicokinetics 21
Chapter 3 Mechanistic Toxicology 45

Section 2: Organ toxicity

Chapter 4 Target Organ Toxicity 65

Section 3: Non-organ-directed toxicity

Chapter 5 Carcinogenicity and Mutagenicity 101

Section 4: Toxic agents

Chapter 6 Toxic Effects of Pesticides and Agrochemicals 119
Chapter 7 Toxic Effects of Metals and Micronutrients 135
Chapter 8 Toxic Effects of Non-metals and Micronutrients 151
Chapter 9 Toxicological Hazards of Solvents, Gases, Vapours,
and Other Chemicals 155
Chapter 10 Hazards of Radiation and Radioactive Materials 163
Chapter 11 Toxicities from Human Drugs 169

Section 5: Plants

Chapter 12 Toxic Effects of Plants 177

Section 6: Poisonous organisms, food and feed toxicity

Chapter 13 Biotoxins and Venomous Organisms 199
Chapter 14 Food Hazards and Feed-Contaminant Toxicity 207
Chapter 15 Mycotoxicoses 221

Section 7: Environmental toxicology

Chapter 16 Pollution and Ecotoxicology 231

Section 8: Applications in toxicology

Chapter 17 Forensic and Clinical Toxicology 255

Section 9: Special topics

Chapter 18 Adverse Effects of Calories 293
Chapter 19 Toxic Effects of Nanoparticles 297
Chapter 20 Occupational Toxicology 301
Chapter 21 Veterinary Drug Residue Hazards 305
Further Reading 309
Index 311

PREFACE

This book entitled Brain Storming Questions in Toxicology serves as a comprehensive and quick reference for various examinations. This book contains multiple-choice questions, true or false/correct or incorrect statements, and match the correct statement, which are widely used in entrance tests, competitive examinations, and at some places in certifying examinations. It is therefore of utmost importance to induct items that not only tests the knowledge, understanding, and application ability of the student but also helps in learning objectives, methods of self-study, and selfassessment. Solving such brainstorming questions could help the crystallization and assimilation of the fundamental principles and applications in drug toxicology, clinical pharmacology, clinical toxicology, and medical toxicology, and for forensic toxicologists, environmentalists, and veterinarians.
Thus, this book will be a useful tool and essential guide for those who want to prepare for licensure and certification exams, persons seeking continuing education, etc. This will also serve as a refresher for academicians and professionals in the field. With these objectives, the book has been divided in several chapters that cover the general principles of toxicology, disposition and kinetics, mechanistic toxicology, target and non-target-directed toxicity, and the toxic effects of various xenobiotics, such as pesticides, metals and micronutrients, non-metals, solvents, gases and vapours, poisonous and venomous organisms, toxicity from humanuse drugs, plant toxins, food and feed contaminants, radiation and radioactive materials, adverse effects of pollution and ecotoxicology, forensic and clinical toxicology, adverse effects of calories, toxic effects of nanomaterials, occupational exposure, and residual drug toxicity. Each chapter is in the format of objective questions and answers; thus, it is a unique book in toxicology that reflects the breadth and multidisciplinary nature of toxicology with an objective approach to the subject.
In brief, the book is an essential guide and has been specifically targeted for a very specific audience of students, teachers, and established toxicologists. Therefore, the author believes that this book will serve the students, academic institutions, and industry as follows:
• It is an excellent contribution for the students who need a study aid for toxicology but wants more than a textbook because they need a self-testing regime.
• It will be a useful tool for the teachers of toxicology who need inspiration when composing questions for their students.
• It will also help established toxicologists test their own knowledge of understanding the subject matter.
• It will be useful at universities and colleges and in industry for in-house training courses in toxicology, which I know exist in some pharmaceutical and chemical companies.
• It is required for all those who want to study for the toxicology boards and other examinations.
Thus, the main strength of this book is to improve the engagement and understanding of the subject. Toxicology is a rapidly evolving field. Suggestions and comments are welcome to help the author improve the contents of the book. Please also suggest the deficiencies that need to be covered at drpkg_brly@yahoo.co.in or drpkg1943@gmail.com if you have any topics you feel should be better covered in any future editions.
P. K. Gupta

Chapter 1

PRINCIPLES OF TOXICOLOGY

1.1 MULTIPLE-CHOICE QUESTIONS(Choose the most appropriate response.)
Exercise 1
Q.1. ‘It is the dose that differentiates a toxicant from a poison.’ This statement was made
by scientist ________.
a) Paracelsus
b) Hippocrates
c) Socrates
d) Homer
Q.2. The branch of science that deals with assessing the toxicity of substances of plant and animal
origin and those produced by pathogenic bacteria is ________.
a) toxicology
b) toxinology
c) toxicokinetics
d) toxicodynamics
Q.3. Minimum dose of a toxicant producing the desired response is called ________.
a) ceiling dose
b) threshold dose
c) both a and b
d) none
Q.4. The Arthus reaction is seen in the hypersensitivity of ________.
a) type I
b) type II
c) type III
d) type IV
Q.5. The Coolie breeds of dogs are hypersensitive to ________.
a) Albendazole
b) Ivermectin
c) both
d) none
Q.6. The measure of the margin of safety of a toxicant is obtained by ________.
a) LD50/ED 99
b) LD 1/ED 99
c) ED50/LD 50
d) LD50/ED 50
Q.7. A substance is called as moderately toxic if its median lethal dose is ________.
a) 1–5 mg
b) 5–500 mg
c) 0.5–1 g
d) >1 g
Q.8. A toxic substance produced by a biological system is specially referred to as a ________.
a) toxicant
b) toxin
c) xenobiotic
d) poison
Q.9. Allergic contact dermatitis is ________.
a) a non-immune response caused by a direct action of an agent on the skin
b) an immediate type-I hypersensitivity reaction
c) a delayed type-IV hypersensitivity reaction
d) characterized by the intensity of reaction being proportional to the elicitation dose
e) not involved in photoallergic reactions
Q.10. The reference dose (RfD) is generally determined by applying which of the following
default procedures?
a) An uncertainty factor of 100 is applied to the NOAEL in chronic animal studies
b) A risk factor of 1000 is applied to the NOAEL in chronic animal studies
c) A risk factor of 10,000 is applied to the NOAEL in subchronic animal studies
d) An uncertainty factor between 10,000 and 1 million is applied to the NOEL from
chronic animal studies
e) Multiplying the NOAEL from chronic animal studies by 100
Q.11. Which of the following concerning the use of the ‘benchmark dose’ in risk assessment is
not correct?
a) Can use the full range of doses and responses studied
b) Allows use of data obtained from experiments where a clear ‘no observed adverse
effect level’ (NOAEL) has been attained
c) May be defined as the lower confidence limit on the 10% effective dose
d) Is primarily used for analyses of carcinogenicity data and has limited utility for analyses
of developmental and reproduction studies that generate quantal data
e) Is not limited to the values of the administered doses
Q.12. Administration by oral gavage of a test compound that is highly metabolized by the liver
versus subcutaneous injection will most likely result in ________.
a) less parent compound present in the systemic circulation
b) more local irritation at the site of administration caused by the compound
c) lower levels of metabolites in the systemic circulation
d) more systemic toxicity
e) less systemic toxicity
Q.13. The phrase that best defines ‘toxicodynamics’ is the ________.
a) linkage between exposure and dose
b) linkage between dose and response
c) dynamic nature of toxic effects among various species
d) dose range between desired biological effects and adverse health effects
e) loss of dynamic hearing range due to a toxic exposure
Q.14. Which of the following was banned under the Delaney Clause of the Food Additive
Amendment of 1958?
a) Butylated hydroxytoluene
b) Sulfamethazine
c) Cyclamate
d) Phytoestrogens
e) Aflatoxin
Q.15. Which of the following toxicity can occur from a single exposure?
a) Acute toxicity
b) Subacute toxicity
c) Subchronic toxicity
d) Chronic toxicity
Q.16. Which of the following assumptions is not correct regarding risk assessment for male
reproductive effects in the absence of mechanistic data?
a) An agent that produces an adverse reproductive effect in experimental animals is
assumed to pose a potential reproductive hazard to humans.
b) In general, a non-threshold is assumed for the dose-response curve for male reproductive
toxicity.
c) Effects of xenobiotics on male reproduction are assumed to be similar across species
unless demonstrated otherwise.
d) The most sensitive species should be used to estimate human risk.
e) Reproductive processes are similar across mammalian species.
Q.17. A newly formed hapten protein complex usually stimulates the formation of a significant
amount of antibodies in ________.
a) 1–2 min
b) 1–2 hours
c) 1–2 days
d) 1–2 weeks
Q.18. Prolonged muscle relaxation after succinylcholine is an example of a/an ________.
a) IGE-mediated allergic reaction
b) idiosyncratic reaction
c) immune complex reaction
d) reaction related to a genetic increase in the activity of a liver enzyme
Q.19. Increased production of methemoglobin is due to decreased activity of ________.
a) cytochrome P450 2B6
b) NADH cytochrome b5 reductase
c) cytochrome oxidase
d) cytochrome a3
Q.20. The most common target organ of toxicity is the ________.
a) heart
b) lung
c) CNS (brain and spinal cord)
d) skin
Answers
1. a 6. d 11. d 16. b
2. b 7. b 12. a 17. c
3. b 8. b 13. b 18. d
4. c 9. c 14. c 19. b
5. b 10. a 15. a 20. c 

FURTHER READING
Aiello, Susan E. (2016). The Merck Veterinary Manual, 11th ed. Merck & Co Inc, Kenilworth, NJ.
Beasley, V. (1999). Absorption, distribution, metabolism, and elimination: Differences among
species. In: Veterinary Toxicology, Ed. V. Beasley, International Veterinary Information
Service (www.ivis.org), Ithaca, NY. https://www.researchgate.net/publication/268347521_
Absorption_Distribution_Metabolism_and_Elimination_Differences_Among_Species_9-
Aug-1999.
FAO, Health hazards associated with animal feed. FAO Rome, Section 1, http://www.fao.org/
docrep/012/i1379e/i1379e01.pdf.
Fruncillo, M.D., Richard, J. (2011). 2,000 Toxicology Board Review Questions, Xlibris.
Gupta Ramesh, C. (2018). Veterinary Toxicology: Basic and Clinical Principles, 3rd ed. Academic
Press/Elsevier, San Diego, CA.
Gupta, P.K. (2014). Essential Concepts in Toxicology, BSP Pvt Ltd, Hyderabad, India.
Gupta, P.K. (2016). Fundamental in Toxicology: Essential Concepts and Applications in Toxicology,
1st ed. Elsevier/BSP, London, UK.
Gupta, P.K. (2018). Illustrative Toxicology, 1st ed. Elsevier, San Diego, CA.
Gupta, P.K. (2019). Concepts and Applications in Veterinary Toxicology: An Interactive Guide, 1st
ed. Routledge, London, UK.
Gupta, P.K. Ed. (2010). Modern Toxicology: Adverse Effects of Xenobiotics, Vol. 2, 2nd reprint.
PharmaMed Press, Hyderabad, India.
Gupta, P.K. Ed. (2010). Modern Toxicology: Basis of Organ and Reproduction Toxicity, Vol. 1, 2nd
reprint. PharmaMed Press, Hyderabad, India.
Gupta, P.K. Ed. (2010). Modern Toxicology: Clinical Toxicology, Vol. 3, 2nd reprint. PharmaMed
Press, Hyderabad, India.
Klaassen, C.D. (2019). Casarett and Doull’s Toxicology: The Basic Science of Poisons, 9th ed.
McGraw-Hill, New York.
Klaassen, C.D., Watkins, III JB. Ed. (2015). Casarett & Doull’s Essentials of Toxicology, 3rd ed.
McGraw-Hill, New York.
Renwick, A.G. (2008). Toxicokinetic. In: Hays, A.W. (Ed.), Principles and Methods of Toxicology,
5 ed. Taylor & Francis Groups, Boca Raton, FL.
Sutmoller, P. (1997). Contaminated food of animal origin: Hazards and risk management. OIE
Scientific and Technical Review. 16(2). http://siteresources.worldbank.org/INTARD/ 843432-
1111149860300/20434404/ContaminatedFood.pdf.
Timbrell, J.A. (1997). Study Toxicology Through Questions, 1st ed. Routledge, London, UK.

Saturday, 10 February 2018

Series 7: Multiple Choice Questions and fill in blanks TOXICOLOGY Question and Answer bank by Dr Pawan K (PK) Gupta


INTRODUCTION
TOXICOLOGY Question and Answer bank is aimed to make the study of toxicology simple and understandable ---------------------

Series 7: Multiple Choice Questions and fill in blanks

Multiple Choice Questions

Exercises
Q. 1. Examples of significant concentrations of a toxicant in a tissue that is not a target organ include all of the following except-----------.
a) lead in bone
b) DDT in adipose tissue
c) paraquat in lung
d) TCDD in adipose tissue
Q. 2. the ability of a chemical to cause acute skin and eye irritation is usually evaluated in a ------
a) rabbit
b) rat
c) mouse
d) dog
Q. 3.  before a potential pharmaceutical compound can be given to humans .-------.
a) an NDA must be filed with the FDA
b) an IND must be filled with the FDA
c) acute toxicity studies on 4 species must be conducted
d) a 2-year dog carcinogenicity study must be completed
Q. 4.  phase 1 clinical trials are conducted to determine all of the following except ---
a) pharmacokinetics
b) safety
c) rare adverse effects
d) preliminary efficacy
Q. 5. MTD stands for ------------------
a) minimum tolerated dose
b)maximum total dose
c) maximum tolerated dose
d) maximum threshold dose
Q. 6. the acute toxicity study in animals provides ------
a) an appropriate lethal dose
b) information on target organs
c) information on dose selection for long-term studies
d)all of the above
Q. 7. a subacute toxicity study in rats usually lasts ------.
a) 3 days
b)14 days
c) 3 months
d) 6 months
Q. 8. the period of organogenesis in rats is ---.
a) day 3-10
b) day 7-17
c)  day 12-25
d) day 17-56
Q. 9.  a dose of investigational drug that suppresses body weight gain slightly in a 90-day animal study is defined by some regulatory agencies to be-------.
a) LOAEL
b) NOAEL
c)MTD
d) reference dose
Q. 10. a subchronic animal study required by the FDA will usually include-----
a) two species (usually one rodent and one nonrodents)
b) both genders
c) at least three doses (low, intermediate, and high)
d) all of the above

Q.11 A dose of a compound A is toxic to animals in vivo. Another chemical B is not toxic when given at doses several orders of magnitude higher but when the two are given together the toxic response is greater than that of the given dose of A alone.
a) antagonism
b) synergism
c) additivity
d) potentiation
e) none of the above
Q.12 Which information may be gained from an acute toxicity study
a) no effect level
b) LD50 
c) therapeutic index
d) target organ
e) all of the above
Q.13The therapeutic index is usually defined as
a) TD50 / LD50 
b) ED50 / LD50 
c) LD50   / ED50
d) ED50  / TD50
e) LD50   / ED50
Q.14 1000 ppm is equivalent to 1%
a) True
b) False

Answers
1. c;      2. a;      3. b ;     4.c ;      5.c ;      6.d ;      7.b ;     8.b ;      9.c ;      10. d; 11. d; 12. e; 13. c ; 14. b.

Fill in blanks

Q. 1. The branch of science which deals with the harmful effects of physical and chemical agents of human and animal life is ------------------------------------
Q. 2. In the term toxicology, the word ‘toxicon’ (Greek) means --------------------
Q. 3. The branch of toxicology, which deals with diagnosis, treatment and management of toxic substances, is known as -----------------------------------
Q. 4. The development and interpretation of mandatory toxicology testing programs is addressed by -------------------------------------------
Q. 5 Investigating and controlling the toxic effects of various substances on the community is dealt by ----------------------.
Q. 6. The study of toxicity produced by subsances of plant, animal and microbial origin is termed as -------------
Q. 7. A foreign chemical substance, which is not normally produced in the body or forms a part of the food, is known as --------------------.
Q. 8. The source of adverse effect/ damage is known as ----------------------
Q. 9. The likelyhood/probability of adverse effect upon exposure to a hazard is known as --------------------.
Q. 10. The statement, “all substances are poisons; the dose differentiates poison from a remedy” is associate with -------------------------.

Answers
1.TOXICOLOGY; 2. POISON; 3.CLINICA L TOXICOLOGY; 4. REGULATORY TOX COLOGY; 5 TOXICOVIGILANCE; 6. TOXINOLOGY; 7. XENOIOTIC; 8 HAZARD. (eg: Water containing Fluoride; Here fluoride is the hazard and fluorosis is the adverse effect. Hazard is independent of dose or exposure i.e., it is present whether someone drinks the water or not).
9. RISK. (eg: While drinking water containing fluoride, the chances of getting fluorosis is called risk. Risk can range from 0 to 100% depending on dose and exposure i.e., one should be exposed to a hazard to calculate the risk); 10. PARACELSUS

Exercises
Q. 1 The scientist referred to as ‘Father of Toxicology’ is ------------------------
Q. 2.  DDT (Dichlorodiphenytrichloro ethane) which is used to control malaria and typus was discovered by ----------------------------
Q. 3. The person who is known as ‘Father of Nerve Agents’ is ------------------------------
Q. 4. The author of the book ‘Silent Spring’ in which the detrimental effect of DDT and other pesticides on environment –particularly on birds was document is -------------------------. 
Q. 5. Bhopal gas tragedy, which is considered to be the world’s worst industrial disaster, was caused due to the leakage of------------------------------------ from Union Carbide fertilizer company.
Q. 6. Use of thalidomide in pregnant women for treating women for treating morning sickness led to -------------------------condition in the infants.
Q. 7. If the action of one substance opposes or neutralizes the effect of another substance, the relationship is referred to as -------------------------..
Q. 8. Rodents are preferred for oral toxicity testing as they lack ------------------ reflex.
Q. 9. Maximum acceptable/ permitted amount of a drug present in feed and foods is known as ----------------------------------------------------------------------.
Q. 10. The highest dose of a compound, which produces adverse effects but no mortality is called -----------------------------------------------------------------------.
Answers
1. M.J.B. Orfila; 2. Pau Muller; 3 GERHARD SCHRADER; 4. RACHEL CARSON;5. METHYL-ISOCYANATE (MIC); 6. PHOCOMELIA; ;7. ANTAGONISM (All antidotes have antagonistic relationship with their respective toxicants) have antagonistic relationship with the irrespective toxicants); 8. VOMITION; 9 MAXIMUM RESIDUE LEVEL (MRL). (For pesticides – MAXIMUM RESIDUE LIMIT); 10 MAXIMUM TOLERATED DOSE {(MTD),  MTD is also referred to as LD0 (Zero) as it will cause adverse effects but no mortality)}.

Exercise
Q.1. If the period of exposure of a toxicant is more than 3 months, the type of study is termed as ---------------------.
Q. 2. The type of toxicity which results due to progressive accumulation of a toxicant in the body is known as ------------------------------.
Q. 3. The amount of toxicant in food and water, which can be consumed daily over a life time without any significant health risk, is called as ------------------------------------------.
Q. 4 Unlawful or criminal killing of animals through administration of poisonsis known as -----------------------
Q. 5. Unintentional addition of toxicants and contaminants in feed  and water is known as ----------------------.
Q. 6. Man -made sources of toxicants are referred to as ------------------------ sources.
Q. 7. Genetically determined abnormal reactivity of an individual to a chemical is known as----------------------------..
Q. 8. Failure to elicit a response to an ordinary dose of a substance due prior usage is known as --------------------------.
Q. 9. The beneficial effects of toxic substances at low doses are known as-----------------.
Q. 10. In the event of irreparable injury, the cell undergoes a process of programmed cell death known as ----------------------------.
Q. 11 A substance is classified as extremely toxic if the lethal dose (LD) is LESS THAN ------------- and as practically non-toxic if the LD is ------------.
Q. 12. The ability of a substance to induce cancer is known as ------------------.    

Answers
1. CHRONIC TOXICITY; 2. CUMULATIVE TOXICITY(Several toxicants such as heavy metals, alcohol, DDT etc cause cumulative toxicity.); 3. ACCEPTABLE DAILY INTAKE (ADI); 4. MALICIOUS POISONING; 5. ACCIDENTAL POISONING; 6. ANTHROPOGENIC; 7. IDIOCYNCARY; 8. TOLERANCE(Tolerance is generally caused due to the induction of metabolizing enzymes in liver. However, in case of chronic alcoholism, pseudo-tolerance is observed, due to thickened GIT mucosa, which reduces absorption);

9. HORMESIS; 10. APOPTOSIS(Apoptosis is also involved in number of physiological process such as embryogenesis, ageing, cancer prevention etc); 11. 1mg/kg, 5 to 15 g/kg(It should be remembered that more the LD of a compound, less is its toxicity); 12. CARCINOGENESIS

FURTHER READING

Gupta PK (2018) Illustrative Toxicology with Question bank. 1st Edition. Elsevier, USA

Gupta PK (2016) Fundamentals of Toxicology: Essential concepts and applications. 1st Edition. ISBN-9780128054260, pp 438, BSP/Elsevier, USA

The Merck Veterinary Manual (2016). Chapter “Herbicide Poisoning” by PK GUPTA 11th edition, Merck & Co. Inc Whitehouse Station, NJ, USA  2969-99

The Merck Veterinary Manual (2016). Chapter “Pentachlorophenol Poisoning” by PK GUPTA 11th edition, Merck & Co. Inc Whitehouse Station, NJ, USA  pp 3052-53

Gupta PK (2016) Essential Concepts in Toxicology. Published by PharmaMed Press (A unit of BSP Books Pvt. Ltd), Hyderabad, India pp 362.

Gupta PK (2010) Modern Toxicology, Basis of organ and reproduction toxicity. Vol 1. Published by Pharma  Med Press (A unit of BSP Books Pvt. Ltd). Hyderabad, India pp 1-460.

Gupta PK (2010) Modern Toxicology, Adverse effects of xenobiotics. Vol 2, Published by PharmaMed Press (A unit of BSP Books Pvt. Ltd). Hyderabad, India pp 1-460.

Gupta PK (2010) Modern Toxicology, Immuno and clinicsal toxicology Vol 3. Published by PharmaMed Press (A unit of BSP Books Pvt. Ltd). Hyderabad, India pp 1-340.


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