General Principles of Toxicology

GENERAL PRINCIPLES OF TOXICOLOGY

ROBERT C. JAMES, STEPHEN M. ROBERTS, and PHILLIP L. WILLIAMS

The intent of this chapter is to provide a concise description of the basic principles of

toxicology and to illustrate how these principles are used to make reasonable

judgments about the potential health hazards and the risks associated with chemical

exposures. This chapter explains

• Some basic definitions and terminology

• What toxicologists study, the scientific disciplines they draw upon, and specialized

areas of

interest within toxicology

• Descriptive toxicology and the use of animal studies as the primary basis for hazard

identification, the importance of dose, and the generation of dose–response

relationships

• How dose–response data might be used to assess safety or risk

• Factors that might alter a chemical’s toxicity or the dose–response relationship

• The basic methods for extrapolating dose–response data when developing

exposure guide-

lines of public health interest

1.1 BASIC DEFINITIONS AND TERMINOLOGY

toxic entered the

English language around 1655 from the Late Latin word toxicus (which meant

poisonous), itself

derived from toxikón, an ancient Greek term for poisons into which arrows were

dipped. The early

history of toxicology focused on the understanding and uses of different poisons, and

even today most

people tend to think of poisons as a deadly potion that when ingested causes almost

immediate harm

or death. As toxicology has evolved into a modern science, however, it has

expanded to encompass all

forms of adverse health effects that substances might produce, not just acutely

harmful or lethal effects.

The following definitions reflect this expanded scope of the science of toxicology:

Toxic—having the characteristic of producing an undesirable or adverse health

effect.

Toxicity—any toxic (adverse) effect that a chemical or physical agent might produce

within a living

organism.
Toxicology—the science that deals with the study of the adverse effects (toxicities)

chemicals or

physical agents may produce in living organisms under specific conditions of

exposure. It is

a science that attempts to qualitatively identify all the hazards (i.e., organ toxicities)

associated

with a substance, as well as to quantitatively determine the exposure conditions

under which

those hazards/toxicities are induced. Toxicology is the science that experimentally

investigates

the occurrence, nature, incidence, mechanism, and risk factors for the adverse

effects of toxic

substances.

As these definitions indicate, the toxic responses that form the study of toxicology

span a broad

biologic and physiologic spectrum. Effects of interest may range from something

relatively minor such

as irritation or tearing, to a more serious response like acute and reversible liver or

kidney damage, to

an even more serious and permanent disability such as cirrhosis of the liver or liver

cancer. Given this

unfamiliar with

toxicology to define some additional terms, listed in order of relevance to topics that

might be discussed

in Chapters 2–22 of this book.

Exposure—to cause an adverse effect, a toxicant must first come in contact with an

organism. The

means by which an organism comes in contact with the substance is the route of

exposure

(e.g., in the air, water, soil, food, medication) for that chemical.

Dose—the total amount of a toxicant administered to an organism at specific time

intervals. The

quantity can be further defined in terms of quantity per unit body weight or per body

surface

area.

Internal/absorbed dose—the actual quantity of a toxicant that is absorbed into the

organism and

distributed systemically throughout the body.

Delivered/effective/target organ dose—the amount of toxicant reaching the organ

(known as the

target organ) that is adversely affected by the toxicant.

Often it is considered to be a single exposure (or dose) but may consist of repeated

exposures within a short time period. Subacute exposure—resembles acute

exposure except that the exposure duration is greater, from several days to one

month. Subchronic exposure—exposures repeated or spread over an intermediate

time range. For animal testing, this time range is generally considered to be 1–3

months. Chronic exposure—exposures (either repeated or continuous) over a long

(greater than 3 months) period of time. With animal testing this exposure often

continues for the majority of the experimental animal’s life, and within occupational

settings it is generally considered to be for a number of years.

Acute toxicity—an adverse or undesirable effect that is manifested within a relatively

short time interval ranging from almost immediately to within several days following

exposure (or dosing). An example would be chemical asphyxiation from exposure to

a high concentration of carbon monoxide (CO). Chronic toxicity—a permanent or

lasting adverse effect that is manifested after exposure to a toxicant. An example

would be the development of silicosis following a long-term exposure to silica in

workplaces such as foundries.

Local toxicity—an adverse or undesirable effect that is manifested at the toxicant’s

site of contact

with the organism. Examples include an acid’s ability to cause burning of the eyes,

upper

respiratory tract irritation, and skin burns.

organism or in

an organ with selective vulnerability distant from the point of entry of the toxicant

(i.e.,

toxicant requires absorption and distribution within the organism to produce the toxic

effect).

Examples would be adverse effects on the kidney or central nervous system

resulting from

the chronic ingestion of mercury.

Reversible toxicity—an adverse or undesirable effect that can be reversed once

exposure is stopped.

Reversibility of toxicity depends on a number of factors, including the extent of

exposure

(time and amount of toxicant) and the ability of the affected tissue to repair or

regenerate. An

example includes hepatic toxicity from acute acetaminophen exposure and liver

regeneration.

Delayed or latent toxicity—an adverse or undesirable effect appearing long after the

initiation

and/or cessation of exposure to the toxicant. An example is cervical cancer during

adulthood
resulting from in utero exposure to diethylstilbestrol (DES).

Allergic reaction—a reaction to a toxicant caused by an altered state of the normal

immune

response. The outcome of the exposure can be immediate (anaphylaxis) or delayed

(cell-mediated).

Idiosyncratic reaction—a response to a toxicant occurring at exposure levels much

lower than those

generally required to cause the same effect in most individuals within the population.

This

response is genetically determined, and a good example would be sensitivity to

nitrates due

to deficiency in NADH (reduced-form nicotinamide adenine dinucleotide phosphate)–

methemoglobin reductase.

Mechanism of toxicity—the necessary biologic interactions by which a toxicant exerts

its toxic

effect on an organism. An example is carbon monoxide (CO) asphyxiation due to the

binding

of CO to hemoglobin, thus preventing the transport of oxygen within the blood.

Toxicant—any substance that causes a harmful (or adverse) effect when in contact

with a living

organism at a sufficiently high concentration.

that is, naturally

produced toxicants. An example would be the pyrethrins, which are natural

pesticides

produced by pyrethrum flowers (i.e., certain chrysanthemums) that serve as the

model for the

man made insecticide class pyrethroids.

Hazard—the qualitative nature of the adverse or undesirable effect (i.e., the type of

adverse effect)

resulting from exposure to a particular toxicant or physical agent. For example,

asphyxiation

is the hazard from acute exposures to carbon monoxide (CO).

Safety—the measure or mathematical probability that a specific exposure situation or

dose will not produce a toxic effect. Risk—the measure or probability that a specific

exposure situation or dose will produce a toxic effect. Risk assessment—the process

by which the potential (or probability of) adverse health effects of exposure are

characterized.