Presented by: Robin Johns, PhD, RN, Augusta University
Key Functions:
Growth and development
Sex differentiation
Metabolism
Adaptation to changing environments
Important Roles:
Regulation of digestion
Use and storage of nutrients
Electrolyte and water metabolism
Reproductive functions
Adipose Tissue:
Largest endocrine organ in the body
Hormones:
Specialized organic molecules acting as chemical messengers
Travel through blood to target sites
Can act locally (paracrine or autocrine)
Present in body fluids at all times
Characteristics:
A single hormone can have various effects in different tissues
A single function can be regulated by multiple hormones
Interaction:
Hormones (signals) interact with receptors on target cells
Release of signals occurs from glands
Involves second messenger systems
Regulation Types:
Diurnal: Fluctuates with sleep-wake cycles (e.g., GH, ACTH)
Cyclic: Secreted in a cyclic manner (e.g., female sex hormones)
Feedback Mechanisms:
Monitor substances like glucose (insulin) and water (ADH)
Involves hypothalamic-pituitary-target cell systems
Factors Affecting Control:
Positive feedback
Negative feedback
Response Factors:
Number of receptors (up-regulation/down-regulation)
Affinity of receptors for hormones
Conditions affecting affinity (e.g., pH levels)
Hypothalamus:
Coordinating center for endocrine and autonomic functions
Hypothalamic Hormones:
GHRH, Somatostatin, Dopamine, TRH, CRH, GnRH
Anterior Pituitary Cell Types:
Thyrotrophs (TSH), Corticotrophs (ACTH), Gonadotrophs (LH, FSH), Somatotrophs (GH), Lactotrophs (Prolactin)
Hormonal Functions:
GH: Body growth and metabolism
TSH: Thyroid function
ACTH: Glucocorticoid hormone levels
FSH & LH: Gonadal function
Prolactin: Breast growth and milk production
Assessment Measures:
Blood tests, urine tests, stimulation/suppression tests, genetic tests, imaging
Disturbances:
Hypofunction: Underproduction of hormones (causes: congenital defects, aging, receptor defects)
Hyperfunction: Excessive hormone production (causes: stimulation, tumors)
Primary Disorders: Originate in the target gland
Secondary Disorders: Normal target gland function altered by pituitary issues
Tertiary Disorders: Result from hypothalamic dysfunction
Types:
Primary: Originate at the site
Secondary: Metastatic lesions
Functional: Secrete hormones
Nonfunctional: Do not secrete hormones
Conditions:
Hypopituitarism: Gradual onset, can be acute
Hyperpituitarism: Symptoms vary based on hormone overproduction
Key Hormones:
Serum cortisol, prolactin, thyroxine (T4), testosterone/estrogen, GH
Question: Identify primary disorder from gland lesions.
Essential Hormones:
GH, Insulin, Thyroid hormones (T3, T4), Androgens
Growth Hormone Functions:
Linear bone growth, cell size increase, fatty acid usage, carbohydrate reduction
Deficiency: Short stature or dwarfism
Excess: Gigantism
Conditions:
Acromegaly: Overgrowth of cartilage, organ enlargement, metabolic disturbances
Functions:
Increase metabolism, protein synthesis, growth, and development
Alterations:
Hypothyroidism: Decreased metabolism, myxedema, elevated cholesterol
Hyperthyroidism: Increased metabolism, sympathetic responsiveness
Hypothyroidism Symptoms: Sluggishness, cold intolerance, weight gain
Hyperthyroidism Symptoms: Anxiety, tachycardia, weight loss
Diagnostic Measures:
T3, T4, TSH levels, imaging, biopsy
Graves Disease: Autoimmune hyperthyroidism with goiter and ophthalmopathy
Symptoms: High fever, cardiovascular effects, severe CNS effects
Types:
Mineralocorticoids (Aldosterone), Glucocorticoids (Cortisol), Adrenal sex hormones
Conditions:
Addison’s Disease: Primary adrenal insufficiency
Acute Adrenal Crisis: Life-threatening situation
Symptoms: Weight loss, fatigue, gastrointestinal issues, hypotension
Causes: Excessive ACTH production, adrenal tumors
Symptoms: Altered fat metabolism, muscle weakness, glucose derangements
This note summarizes the key points from the transcript on the endocrine system, its functions, hormones,