Exam 2 Flashcards

1
Q

Basic principles of motor function (why do motivational neuroscientists study movement?)

A

Motivational neuroscientists study movement to understand how behavior is linked to motivation, emotion, and decision-making. Movement is a key component of how organisms interact with their environment, acquire resources, and respond to challenges. By studying movement, researchers can gain insights into neural mechanisms underlying behavior and motivation.

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2
Q

Reflexive Movements (Different Kinds of Movements and the Order of Motor Control)

A

Involuntary, automatic responses to stimuli (e.g., withdrawal reflex).

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3
Q

Voluntary (Different Kinds of Movements and the Order of Motor Control)

A

Conscious, planned actions (e.g., reaching for an object)

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4
Q

Rhythmic (Different Kinds of Movements and the Order of Motor Control)

A

Repetitive actions (e.g., walking, running).

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5
Q

Spinal Cord and lower motor neurons (Hierarchy of Movement)

A

The spinal cord contains lower motor neurons that directly innervate skeletal muscles, facilitating basic reflexes and movements.

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6
Q

Brainstem and Cerebellum (Hierarchy of Movement)

A

The brainstem integrates sensory information and coordinates basic movements, while the cerebellum fine-tunes motor activity, balance, and timing.

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7
Q

Basal Banglia (Hierarchy of Movement)

A

Basal Ganglia: Involved in action selection, sequencing of movements, and motivational aspects of movement. They help initiate and regulate voluntary motor activity.

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8
Q

Cortical Region (Hierarchy of Movement)

A

Cortical Regions: The primary motor cortex initiates voluntary movements, while the premotor cortex is involved in planning and coordinating complex movements.

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9
Q

Spinal Cord (Areas of the brain and movement)

A

Spinal Cord and Lower Motor Neurons: Responsible for reflex actions and transmitting signals to muscles.

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10
Q

Cerebellum (areas of the brain and movement)

A

Cerebellum: Coordinates smooth and precise movements, motor learning, and timing.

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11
Q

Brain stem (areas of the brain and movement)

A

Brainstem: Regulates basic bodily functions and integrates motor pathways.

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12
Q

Basal ganglia (areas of the brain and movement)

A

Basal Ganglia: Facilitates the initiation and suppression of movements, essential for action planning and motivation.

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13
Q

Cortical Regions (areas of the brain and movement)

A

Cortical Regions:
Primary Motor Cortex (M1): Directly controls voluntary movements.
Premotor Cortex: Involved in planning and executing movement sequences.

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14
Q

Ethology and Movement

A

Ethology is the scientific study of animal behavior, focusing on how animals interact with their environments and the biological significance of their movements.

Definition and Areas of Study

Definition: Ethology examines behaviors in natural contexts, often focusing on instinctual and learned behaviors.

Areas of Study: Includes communication, foraging, mating behaviors, and territoriality, exploring how movement relates to survival and reproductive success.

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15
Q

Types of Motor Patterns (Ethology)

A

Ethology looks at:

Fixed Action Patterns (FAPs): Stereotypical sequences of movements triggered by specific stimuli (e.g., courtship dances).
Learned behaviors: How animals adapt their movement based on experience.

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16
Q

Types of Motor Patterns (Ethology)

A

Ethology looks at:

Fixed Action Patterns (FAPs): Stereotypical sequences of movements triggered by specific stimuli (e.g., courtship dances).
Learned behaviors: How animals adapt their movement based on experience.

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17
Q

Experimental Work in Ethology

A

Research often involves:

Observational studies in natural settings to understand movement and behavior.
Controlled experiments to test hypotheses about movement patterns and their adaptive significance.

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18
Q

Motivation

A

the processes that initiate, guide, and maintain goal-oriented behaviors. It involves the interplay of biological, emotional, social, and cognitive forces.

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19
Q

Key properties of MOTIVATION include:

A

Direction: The goal or outcome toward which behavior is directed.
Intensity: The energy and effort put forth in pursuing a goal.
Persistence: The duration of effort towards achieving a goal despite obstacles.

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20
Q

Arousal Theory (Theories of Motivation)

A

Arousal Theory: Suggests that people are motivated to maintain an optimal level of arousal, which varies by individual and situation.
Advantages: Explains behaviors beyond basic needs (e.g., thrill-seeking).
Disadvantages: Does not account for why some individuals seek low arousal.

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21
Q

Instinct Theory (Theories of motivation)

A

Instinct Theory: Proposes that certain behaviors are innate and driven by biological instincts.
Advantages: Highlights the role of evolution in behavior.
Disadvantages: Lacks empirical support; oversimplifies complex behaviors.

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22
Q

Drive/Homeostasis Theory (Theories of Motivation)

A

Drive/ Homeostasis Theory: Focuses on maintaining balance (homeostasis) within the body, suggesting that unmet biological needs create drives to restore balance.
Advantages: Explains physiological drives (e.g., hunger, thirst).
Disadvantages: Does not fully explain behaviors that are not directly linked to homeostatic needs.

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23
Q

Incentive Theory (Theories of motivation)

A

Incentive Theory: Suggests that behavior is motivated by external rewards and incentives rather than internal drives alone.
Advantages: Accounts for the influence of external factors on behavior.
Disadvantages: May underestimate the role of intrinsic motivation.

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24
Q

Homeostasis and Related Concepts

A

Homeostasis: The process by which biological systems maintain stability while adjusting to conditions that are optimal for survival.
Set Points vs. Settling Points:
Set Points: Predetermined levels of physiological variables (e.g., body temperature, weight).
Settling Points: More flexible, representing a range around which levels can fluctuate based on various factors, including environmental influences.

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25
Q

Drive Reduction Theory

A

Hydraulic Model: Describes how unmet needs build up pressure (drive) until they are satisfied, which reduces tension and restores homeostasis.
Drives and Psychological Needs: Drives (e.g., hunger, thirst) arise from unmet physiological needs, while psychological needs (e.g., achievement, affiliation) can also motivate behavior.

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26
Q

Intervening Variables and Central Motive States

A

Intervening Variables: Factors that influence the relationship between a stimulus and a response (e.g., cognitive appraisal).
Central Motive State: Refers to an internal state that drives behavior, integrating various needs and motivations.

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27
Q

Biological Basis of Motivation

A

Research explores the neural mechanisms underlying motivation, examining how brain structures and neurochemicals regulate motivated behavior.

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28
Q

Incentive Motivation Theory

A

Suggests that external rewards and incentives shape motivation. The anticipation of rewards influences behavior and can enhance motivation.
Expectations and Motivation: Individuals are motivated by the expected outcomes of their actions, which can influence their persistence and effort.

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29
Q

Key Brain Regions Involved in Reward Processing

A

Ventral Tegmental Area (VTA): Critical for the release of dopamine, involved in reward anticipation.
Nucleus Accumbens: Plays a key role in the processing of rewards and reinforcement.
Prefrontal Cortex: Involved in decision-making and evaluating potential rewards.
Amygdala: Important for emotional responses related to rewards.
Wanting vs. Liking:
Wanting refers to the desire for a reward, often linked to dopamine activity.
Liking relates to the pleasure experienced when obtaining a reward, associated with other neurotransmitters (e.g., opioids).

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30
Q

Ventral Tegmental Area (VTA) (Reward processing)

A

Ventral Tegmental Area (VTA): Critical for the release of dopamine, involved in reward anticipation.

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31
Q

Nucleus Accumbens (Reward processing)

A

Nucleus Accumbens: Plays a key role in the processing of rewards and reinforcement.

32
Q

Prefrontal Cortex (Reward Processing)

A

Prefrontal Cortex: Involved in decision-making and evaluating potential rewards.

33
Q

Amygdala (Reward Processing)

A

Amygdala: Important for emotional responses related to rewards.

34
Q

Homeostasis and Homeostatic Models

A

Homeostasis: The body’s ability to maintain stable internal conditions despite external changes.
Homeostatic Models: Frameworks that describe how physiological systems regulate variables (e.g., hunger, energy balance) to achieve stability.

35
Q

Glucostat and Lipostat

A

Glucostat: Mechanisms that regulate blood glucose levels. Signals like insulin and glucagon help maintain glucose homeostasis.
Lipostat: Mechanisms that monitor fat storage and regulate energy intake and expenditure, with leptin as a key hormone indicating fat levels.

36
Q

Appetite

A

The desire to eat, influenced by physiological, psychological, and environmental factors.

37
Q

Palatability and Taste

A

Palatability: The pleasantness of food, which influences appetite and food choices.
Taste: The sensory experience derived from the interaction of food with taste buds, affecting food preferences and intake.

38
Q

Satiety

A

The feeling of fullness that suppresses the desire to eat, often following a meal.

39
Q

Digestion

A

The process by which food is broken down into absorbable units, allowing nutrients to enter the bloodstream.

40
Q

Macronutrients

A

Fats (Lipids): Important for energy storage and cellular functions.
Amino Acids: Building blocks of proteins, essential for growth and repair.
Glucose: A primary energy source derived from carbohydrates.
Carbohydrates: Sugars and starches that provide energy.
Protein: Necessary for tissue repair and enzyme functions.

41
Q

Phases of Digestion

A

Cephalic Phase: Anticipatory response triggered by the sight, smell, or thought of food.
Gastric Phase: Digestion in the stomach involving mechanical and chemical breakdown.
Intestinal Phase: Digestion and absorption of nutrients in the small intestine.

42
Q

Key Factors Influencing Feeding (perspectives and clinical implications)

A

Physiological Signals: Hormones (e.g., ghrelin stimulates hunger, while leptin promotes satiety) and nutrient levels.
Environmental Cues: Availability of food, social contexts, and sensory stimuli can trigger eating behaviors.

43
Q

Hypothalamus and Feeding (perspectives and clinical implications)

A

Hypothalamus: A critical brain region in regulating hunger and satiety.
Subregions involved in feeding:
Lateral Hypothalamus: Stimulates hunger and feeding.
Ventromedial Hypothalamus: Promotes satiety and inhibits hunger.

44
Q

Eating Disorders and Hormones (perspectives and clinical implications)

A

Obesity: Characterized by excessive body fat; defined biologically by BMI and societally by stigma and health implications.
Neural Changes in Eating Disorders: Alterations in brain structure and function, particularly in reward pathways, decision-making areas, and homeostatic controls, can be seen in conditions like obesity.

45
Q

Biomedical-Based Treatments (perspectives and clinical implications)

A

Bariatric Surgery: Surgical procedures that reduce stomach size or alter the digestive tract to promote weight loss in obese individuals.
Hormonal Treatments: Use of hormones like GLP-1 or leptin to regulate appetite and metabolism.
Medications: Pharmacological approaches (e.g., appetite suppressants) to aid in weight management and treatment of eating disorders.

46
Q

Sexual Behavior

A

Definitions: Sexual behavior can be defined broadly as actions that promote reproduction, including mating, courtship, and various sexual activities. It can also be defined through biological, psychological, and social lenses.

47
Q

Measuring Sexual Behaviours

A

Measuring Sexual Behavior: In animal models, researchers often measure sexual behavior through:
Observational methods: Recording mating rituals and frequency.
Physiological measures: Monitoring hormone levels and physical responses (e.g., genital arousal).
Behavioral assays: Tests designed to assess sexual motivation and preference.

48
Q

Phases of Sex and Behavioral Order

A

Appetitive Phase: Preparation for sexual activity, including courtship and arousal.
Consummatory Phase: The act of sexual intercourse itself.
Post-Copulatory Phase: Behaviors following mating, such as bonding or caregiving.
The sequence of these phases is critical; disruptions can affect reproductive success and behavioral outcomes.

49
Q

Phases of Sex Motivation

A

Motivational Phases:
Initiation: Desire to engage in sexual activity.
Sustained Arousal: Maintenance of interest and physical arousal during sexual behavior.
Satisfaction: Completion and emotional response post-coitus.
These phases are interrelated; for example, effective initiation depends on prior arousal.

50
Q

Sexual Dimorphism (Biology of Sex: Dimorphisms and Brain Basis)

A

Sexual Dimorphism: Refers to differences between males and females in body size, shape, and behavior, often influenced by hormones.

51
Q

Brain Basis (Biology of sex: dimorphism and brain basis)

A

Certain brain regions exhibit sexual dimorphism, affecting behavior and motivation related to sex.

52
Q

Organizational vs. Activational Effects (Biology of Sex: Dimorphisms and Brain Basis)

A

Organizational Effects: Long-lasting changes that occur during critical periods of development (e.g., prenatal hormone exposure affecting brain structure).
Activational Effects: Immediate effects of hormones that influence behavior in adulthood (e.g., testosterone increasing sexual motivation).

53
Q

Brain Mechanisms of Sexual Behavior (hypothalamus & forebrain)

A

Hypothalamus: Plays a crucial role in regulating sexual behavior by integrating hormonal signals and controlling sexual motivation.
Forebrain Regions: Other areas, such as the amygdala and ventral striatum, are involved in processing emotional and reward aspects of sexual behavior.
These regions work together to coordinate appetitive behaviors (e.g., seeking out partners) and consummatory behaviors (e.g., engaging in copulation).

54
Q

Sexual Disorders and Holistic Treatments

A

Sexual Disorders: Conditions that impair sexual function or desire.

Holistic approaches consider psychological, relational, and biological factors in treatment.

Bottom-up treatments might include hormone therapy, psychotherapy, and addressing physical health to improve sexual function.

55
Q

Sexual Disorders and Holistic Treatments

A

Sexual Disorders: Conditions that impair sexual function or desire.

Holistic approaches consider psychological, relational, and biological factors in treatment.

Bottom-up treatments might include hormone therapy, psychotherapy, and addressing physical health to improve sexual function.

56
Q

Exceptional Human Sexual Development Cases

A

Turner Syndrome: A condition where females have a missing or incomplete X chromosome, leading to developmental issues and infertility.

Androgen Insensitivity Syndrome (AIS): A condition where individuals with XY chromosomes develop female characteristics due to a lack of response to androgens. They typically have female genitalia but may lack a uterus.

Congenital Adrenal Hyperplasia (CAH): A genetic disorder affecting adrenal hormone production, leading to increased androgen levels in females, which can cause ambiguous genitalia and other masculinizing traits.

57
Q

Insels Paper (summary)

A

Insel’s review emphasizes the importance of oxytocin and vasopressin in social behaviors, particularly maternal care and pair-bonding. The paper highlights both animal models and human research to illustrate how these hormones facilitate social connections and the complexities of human social behavior. The exploration of receptive and expressive processes, along with the concept of “dark matter,” suggests that understanding social neuroscience requires a deeper examination of the biological underpinnings of social interactions.

58
Q

Receptive vs. Expressive Processes (INSEL’S PAPER)

A

Receptive vs. Expressive Processes: Insel differentiates between receptive processes (how individuals receive social signals) and expressive processes (how individuals communicate and express emotions). He emphasizes that both processes are critical for understanding social behavior.

59
Q

Dark Matter of Social Science (INSEL’S PAPER)

A

This term refers to the underlying, often unmeasured biological mechanisms that contribute to social behavior but are not immediately observable. It suggests that there is much about the neurobiology of social interactions that remains unexplored or poorly understood, much like dark matter in physics.

60
Q

Maternal Care (Key Studies and Support for Oxytocin and Vasopressin) - Insel Paper

A

Animal Models: Studies have shown that oxytocin plays a critical role in maternal behaviors. For example, when researchers manipulate oxytocin levels in rodent models, they observe significant changes in maternal care behaviors, such as licking and grooming of pups.

Brain Manipulations: Lesion studies in the hypothalamus (where oxytocin is produced) reveal that disruptions in oxytocin signaling can lead to deficits in maternal behaviors, indicating its essential role in nurturing and bonding.

61
Q

Pair-Bonding and Affiliative Behaviour (Prairie Voles and humans)- Insel paper

Relates to Key Studies and Support for Oxytocin and Vasopressin

A

Prairie Vole Model: Prairie voles are well-studied for their monogamous pair-bonding behavior. Research has shown that oxytocin and vasopressin are crucial in forming and maintaining these bonds.
When prairie voles are given oxytocin or vasopressin, their affiliative behaviors (like grooming and cuddling) increase, enhancing pair-bond formation.
Conversely, blocking oxytocin receptors disrupts bonding and partner preference, demonstrating the hormone’s vital role.

Related Human Research: In humans, oxytocin has been linked to behaviors such as trust, empathy, and social bonding. Studies show that intranasal administration of oxytocin can enhance prosocial behaviors and increase feelings of closeness and trust in social interactions.

62
Q

Psychopharmacology in the Neuroscience of Motives and Emotions

A

Integration with Neuroscience: Psychopharmacology studies how drugs affect the brain and behavior, specifically in relation to motives (the drives behind actions) and emotions (the feelings that influence behavior). Understanding the neurochemical basis of these processes can illuminate how drugs can alter mood, motivation, and overall behavior.

Emotional and Motivational Pathways: Many drugs affect neurotransmitter systems that are crucial for regulating emotions and motivations, such as dopamine (reward and pleasure), serotonin (mood regulation), and norepinephrine (arousal and alertness).

63
Q

Basics of Pharmacology in Studying Drug Effects

A

Methods: Researchers use various methods to study drug effects on behavior, including:
Animal Models: Behavioral assays (e.g., operant conditioning tasks) assess the effects of drugs on motivation and behavior.
Clinical Trials: Controlled studies in humans to evaluate the efficacy and safety of medications.
Neuroimaging: Techniques like fMRI and PET scans help visualize brain activity and chemical changes in response to drugs.

64
Q

Drug/Medication Types and Their Effects

A

Categories:
Stimulants (e.g., cocaine, amphetamines): Increase alertness and energy, often enhancing dopamine activity. Can lead to tolerance and withdrawal symptoms such as fatigue and depression.

Depressants (e.g., alcohol, benzodiazepines): Decrease arousal and reduce anxiety. Tolerance can develop, and withdrawal may involve anxiety, tremors, and seizures.

Hallucinogens (e.g., LSD, psilocybin): Alter perception and mood without typical withdrawal symptoms but can cause psychological distress.

Opioids (e.g., heroin, morphine): Provide pain relief and euphoria. Highly addictive, with severe withdrawal symptoms including pain, nausea, and cravings.

65
Q

Tolerance and Withdrawal

A

Tolerance: A process where increasing amounts of a drug are needed to achieve the same effects due to the body’s adaptation to the drug.

Withdrawal: Symptoms that occur when a drug is reduced or discontinued, often opposite to the drug’s effects and can lead to cravings and relapse.

66
Q

Sensitization and Drug Addiction

A

Sensitization: Refers to an increased response to a drug following repeated use, often associated with the drug’s effects on motivational and reward pathways. This can enhance cravings and increase the likelihood of relapse.

Addiction: Characterized by compulsive drug-seeking behavior and use despite harmful consequences, often linked to neuroadaptations in reward pathways.

67
Q

Brain Model of Drug Addiction

A

Phases of Addiction: The model often includes three phases:

Binge/Intoxication Phase: Initial use characterized by the activation of the brain’s reward system (mainly involving dopamine).

Withdrawal/Negative Affect Phase: Withdrawal symptoms emerge, creating a cycle of negative emotions and cravings.

Preoccupation/Anticipation Phase: Intense cravings and planning for drug use, often influenced by environmental cues and memories.

68
Q

Treatment Approaches:

A

Pharmacotherapy: Medications (e.g., methadone for opioid addiction) that help manage withdrawal symptoms and reduce cravings.

Behavioral Therapies: Techniques that address the psychological aspects of addiction, such as cognitive-behavioral therapy (CBT) and contingency management.

Support Systems: Involvement of social support and rehabilitation programs to foster recovery and prevent relapse.

69
Q

Stomach Signals (levels of eating decisions)

A

The stomach plays a crucial role in signaling hunger and satiety. Stretch receptors in the stomach send signals to the brain when it is empty or full, influencing the decision to eat.

70
Q

Pancreas: Insulin and Glucagon (levels of eating decisions)

A

Insulin: A hormone released by the pancreas in response to increased blood glucose levels (usually after eating). It facilitates the uptake of glucose by cells and helps store excess energy as fat.

Glucagon: Released when blood glucose levels are low, it promotes the release of glucose from stored glycogen in the liver, increasing blood sugar levels.

71
Q

Duodenum (levels of eating decisions)

A

The first part of the small intestine, where food mixes with digestive enzymes. It also releases hormones that signal fullness, playing a key role in regulating appetite.

72
Q

Cholecystokinin (CCK) (levels of eating decisions)

A

A hormone released by the duodenum in response to fat and protein intake. CCK promotes satiety by slowing gastric emptying and sending signals to the brain to reduce hunger.

73
Q

Cholecystokinin (CCK) (levels of eating decisions)

A

A hormone released by the duodenum in response to fat and protein intake. CCK promotes satiety by slowing gastric emptying and sending signals to the brain to reduce hunger.

74
Q

Brain Regions Involved in Eating (levels of eating decisions)

A

Ventromedial Hypothalamus (VMH): Associated with satiety; lesions in this area can lead to overeating and obesity.

Lateral Hypothalamus (LH): Associated with hunger; lesions can result in reduced eating and weight loss.

Arcuate Nucleus: A key region in the hypothalamus that integrates signals related to energy balance, including those from leptin and ghrelin.

Paraventricular Nucleus (PVN): Involved in regulating energy expenditure and food intake; responds to various hormonal signals to influence appetite.

75
Q

Hormones Involved in Appetite Regulation

A

Insulin: Helps regulate blood sugar levels and signals satiety.

Glucagon: Counteracts insulin, increasing blood sugar when needed.

Leptin: Secreted by adipose (fat) tissue; signals to the brain about energy storage and helps regulate body weight. High levels typically suppress appetite.

Cholecystokinin (CCK): Signals fullness and aids in digestion.
Neuropeptide Y (NPY): A potent appetite stimulant produced in the brain, particularly during energy deficits.

76
Q

Sham Eating:

A

An experimental procedure where an animal is allowed to eat without the food being absorbed (e.g., food is removed before digestion). This helps researchers study the sensory and cognitive aspects of eating without physiological feedback.

77
Q

Sensory Specific Satiety:

A

The phenomenon where the desire to eat specific foods decreases after consumption, leading to a preference for different foods. This helps promote dietary variety and encourages continued eating.