Which of the following is NOT listed as a factor that can contribute to dysbiosis?
A. Excessive or inappropriate use of antibiotics
B. Frequent use of antacids
C. Increased intake of sugar or protein
D. Regular physical exercise
D. Regular physical exercise
Exposure to which combination of factors is associated with the development of dysbiosis?
A. Chronic stress, artificial sweeteners, and pesticide exposure
B. High fiber intake, probiotics, and reduced alcohol consumption
C. Increased sleep duration and low protein intake
D. Vitamin supplementation and balanced nutrition
A. Chronic stress, artificial sweeteners, and pesticide exposure
Exposure to which combination of factors is associated with the development of dysbiosis?
A)Poor dental hygiene
B) anxiety
C) both a and b
D)Vitamin supplementation
C) both a and b
The gut–brain axis is best defined as:
A. Unidirectional signaling from the brain to the gut
B. Communication between the enteric nervous system only
C. Bidirectional communication between the central nervous system and gut microbiota
D. Hormonal signaling limited to the digestive tract
C. Bidirectional communication between the central nervous system and gut microbiota
Which of the following substances released from the gut can signal to the brain?
A. Hormones, neurotransmitters, and immunological factors
B. Digestive enzymes only
C. Bile salts and fatty acids only
D. Vitamins and minerals only
A. Hormones, neurotransmitters, and immunological factors
Signals from the gut to the brain may reach the CNS:
A. Only through the bloodstream
B. Only through the vagus nerve
C. Directly or via autonomic neurons
D. Only through immune cells
C. Directly or via autonomic neurons
Which of the following functions is regulated by the vagus nerve?
A. Voluntary skeletal muscle movement
B. Regulation of digestion, heart rate, and respiratory rate
C. Visual and auditory processing
D. Thermoregulation via brown adipose tissue
B. Regulation of digestion, heart rate, and respiratory rate
Which reflex action is mediated by the vagus nerve?
A. Pupillary light reflex
B. Knee-jerk reflex
C. Swallowing
D. Stretch reflex
C. Swallowing
What evidence supports the role of the vagus nerve in microbiota–brain communication?
A. Increased immune signaling in germ-free mice
B. Neurochemical and behavioral effects persisted after vagotomy
C. Neurochemical and behavioral effects were absent in vagotomized mice
D. Microbiota signals bypass the nervous system
C. Neurochemical and behavioral effects were absent in vagotomized mice
The gut–brain connection involves chemicals called neurotransmitters that primarily regulate:
A. Digestion and nutrient absorption
B. Immune cell differentiation
C. Feelings and emotions
D. Blood pressure and heart rate
C. Feelings and emotions
Which statement about neurotransmitter production is correct?
A. Neurotransmitters are produced only in the brain
B. Gut cells and microbes can produce neurotransmitters
C. Only immune cells produce neurotransmitters
D. Neurotransmitters are produced exclusively by neurons
B. Gut cells and microbes can produce neurotransmitters
A large proportion of which neurotransmitter is produced in the gut?
A. Dopamine
B. GABA
C. Serotonin
D. Norepinephrine
C. Serotonin
Gamma-aminobutyric acid (GABA) is primarily involved in regulating:
A. Appetite and digestion
B. Fear and anxiety
C. Motor coordination
D. Sleep–wake cycles
B. Fear and anxiety
Studies in mice show that probiotics such as Lactobacillus and Bifidobacterium can:
A. Eliminate serotonin production
B. Decrease GABA production
C. Increase GABA production and reduce anxiety- and depression-like behavior
D. Increase stress hormone secretion
C. Increase GABA production and reduce anxiety- and depression-like behavior
Which function of the gut–brain axis involves regulation of peristalsis and enzyme secretion?
A. Cognitive function
B. Energy homeostasis
C. Digestion and motility
D. Immune modulation
C. Digestion and motility
The gut–brain axis helps maintain energy homeostasis by regulating:
A. Blood oxygen levels and ventilation
B. Hunger, satiety, food preferences, and metabolism
C. Electrolyte balance only
D. Circadian rhythms
B. Hunger, satiety, food preferences, and metabolism
Gut microbiota can influence the body’s stress response primarily through which system?
A. Renin–angiotensin system
B. Sympathetic–adrenal–medullary axis
C. Hypothalamic–pituitary–adrenal (HPA) axis
D. Parasympathetic reflex arcs
C. Hypothalamic–pituitary–adrenal (HPA) axis
Dysbiosis of the gut microbiota has been associated with changes in:
A. Vision and hearing
B. Mood, anxiety, depression, and pain sensitivity
C. Muscle strength only
D. Bone density
B. Mood, anxiety, depression, and pain sensitivity
Chronic gut-driven inflammation may impact brain function and contribute to:
A. Improved memory formation
B. Neurodegenerative disorders
C. Increased synaptic plasticity
D. Reduced immune surveillance
B. Neurodegenerative disorders
Which cognitive processes are influenced by gut microbiota and their metabolites?
A. Reflexes only
B. Brain development, learning, memory, and synaptic plasticity
C. Motor neuron firing rates exclusively
D. Visual acuity
B. Brain development, learning, memory, and synaptic plasticity
Functions of SCFAc:Acetate
Most Abundant and Systemic SCFA
Energy and Lipid Metabolism: muscle brain and hear
Appetite and Metabolic Regulation- stimulates hormones like GLP-1 and PYY
Cross-Talk With the Brain- influences hypothalamic control of appetite and neurotransmitter balance.
Immune Modulation- Promotes regulatory T cell (Treg) development and suppresses pro-inflammatory cytokine release
Propionate
Gluconeogenic and Immune-Modulating SCFA
Liver Gluconeogenesis- serves as a substrate for glucose production in liver
Lipid and Cholesterol Regulation Inhibits hepatic cholesterol synthesis
Immune and Inflammatory Control- suppresses inflammation, enhances Treg differentiation, and balances Th17/Treg responses.
Gut–Brain Communication Activates vagal afferents and modulates serotonin and dopamine signaling.
Can influence satiety and energy balance through gut hormone release.
Butyrate
Colon’s Primary Fuel and Barrier Protector
Energy Source for Colonocytes- supports epithelial integrity and oxygen balance (reducing inflammation-prone conditions).
Maintaining Gut Barrier Integrity- Strengthens tight junction proteins → prevents “leaky gut.”
Anti-inflammatory and Epigenetic Regulation Inhibits histone deacetylases (HDACs) → affects gene expression.
Promotes Treg cell expansion and reduces pro-inflammatory cytokines.
Neuroprotective and Mood Effects - modulates microglial activity and neurotrophic factors (like BDNF).
Linked to reduced anxiety- and depression-like behaviors in animal models
Lipopolysaccharide (LPS) is best described as:
A. A neurotransmitter produced by gut microbes
B. A hormone secreted by intestinal cells
C. An inflammatory toxin produced by certain bacteria
D. An anti-inflammatory metabolite
C. An inflammatory toxin produced by certain bacteria