Units 8-12 Practice Flashcards: Case Studies and Clinical Applications

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A comprehensive set of vocabulary flashcards covering Units 8 through 12, focusing on homeostatic mechanisms, neurophysiology, muscle pathology, and various clinical case studies derived from the lecture notes.

Last updated 8:56 PM on 8/3/26
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47 Terms

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Homeostasis

The relative constancy of the chemical composition of blood and extracellular fluid despite external variation, a term coined by Walter Cannon.

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Internal Environment

The concept proposed by Claude Bernard that vertebrates maintain internal constancy to allow tight regulation of cellular metabolism.

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Resting Membrane Potential (VmV_m)

The electrical potential across a cell membrane, measured at 70mV-70\,mV on average, sitting between 65mV-65\,mV and 85mV-85\,mV because roughly 30%30\% of K+K^+ leak channels remain open.

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Potassium (K+K^+) Gradient

The concentration difference where intracellular [K+][K^+] is 150mEq/L150\,mEq/L and extracellular [K+][K^+] is 5mEq/L5\,mEq/L, resulting in an equilibrium potential (EKE_K) of 90mV-90\,mV.

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Acute Gastroenteritis & Cholera Pathophysiology

Infection causing severe diarrhea leading to loss of Na+Na^+, H2OH_2O, malnutrition, and metabolic acidosis.

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Oral Rehydration Therapy (ORT)

A treatment including glucose to co-transport Na+Na^+ across the intestinal epithelium via Na+/glucoseNa^+/\text{glucose} symporters, pulling water back into the body by osmosis.

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Hyperkalemia

Abnormally high plasma [K+][K^+] which depolarizes the resting membrane potential closer to threshold, initially causing hyperexcitability but ultimately disrupting repolarization and causing ECG abnormalities.

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Hypokalemia

Abnormally low plasma [K+][K^+] which hyperpolarizes the resting potential further from threshold, making cells harder to excite and causing muscle weakness.

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Guillain-Barré Syndrome

A T-cell-mediated autoimmune attack against peripheral nervous system (PNS) myelin sheaths, leading to motor neuron dysfunction and progressive muscle weakness.

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Multiple Sclerosis (MS)

An autoimmune disorder where T-lymphocytes and macrophages breach the blood-brain barrier to attack central nervous system (CNS) myelin sheaths, leading to neuroglia scarring (plaques) and axonal degeneration.

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Local Anesthetics (e.g., Procaine, Cocaine)

Drugs that reversibly bind and block voltage-gated Na+Na^+ channels in axonal membranes, preventing depolarization and action potential generation.

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SNARE Complex

A group of proteins that interact with synaptotagmin and Ca2+Ca^{2+} to trigger vesicle exocytosis of neurotransmitters into the synaptic cleft.

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Tetanus Toxin

A bacterial neurotoxin that cleaves SNARE proteins in inhibitory interneurons releasing GABA/glycine, resulting in uninhibited motor firing and spastic paralysis.

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Botulinum Toxin

A toxin that cleaves SNARE proteins at excitatory neuromuscular junctions, blocking acetylcholine (ACh) release and producing flaccid paralysis.

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Myasthenia Gravis

A condition where autoantibodies bind and block or destroy post-synaptic nicotinic ACh receptors at the motor endplate of skeletal muscle.

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Organophosphates & Nerve Gas

Chemicals that irreversibly inhibit Acetylcholinesterase (AChE), causing massive ACh accumulation and lethal cholinergic overstimulation.

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MAO Inhibitors Mechanism

Drugs that block Monoamine Oxidase to prevent the degradation of dopamine, serotonin, epinephrine, and norepinephrine.

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Benzodiazepines (e.g., Valium, Xanax)

Drugs that allosterically bind GABAAGABA_A receptors to increase ClCl^- influx, hyperpolarizing post-synaptic membranes to depress CNS activity.

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Excitotoxicity

A pathological process where excessive glutamate release hyper-activates receptors, causing massive intracellular Ca2+Ca^{2+} influx and neuronal apoptosis, observed in ischemic stroke and ALS.

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Duchenne Muscular Dystrophy (DMD)

An X-linked recessive mutation in the dystrophin gene which anchors myofibrils to the sarcolemma; contraction stress causes sarcolemma tears and muscle necrosis.

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Rhabdomyolysis

The breakdown of muscle fibers due to trauma or extreme exertion, releasing Creatine Kinase (CK-MM isoenzyme) and myoglobin into the blood.

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Amyotrophic Lateral Sclerosis (ALS)

Progressive neurodegeneration of both Upper Motor Neurons (UMN) and Lower Motor Neurons (LMN) often involving superoxide dismutase (SOD1) mutations and ROS damage.

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Spastic Paralysis

Paralysis caused by UMN or descending tract damage, removing inhibitory control over spinal $\gamma$-motor neurons and leading to hyperreflexia and clonus.

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Calcium Channel Blockers

Pharmacological agents that block L-type voltage-gated Ca2+Ca^{2+} channels; dihydropyridines act on vascular smooth muscle, while Verapamil acts on cardiac pacemaker activity.

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Huntington's Disease

An autosomal dominant mutation involving CAG expansion in the HTT gene on chromosome 4, leading to loss of GABAergic/cholinergic neurons and involuntary chorea.

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Parkinson's Disease

A movement disorder caused by the degeneration of dopaminergic neurons in the substantia nigra of the midbrain.

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Cerebellar Ataxia

Loss of voluntary coordination and a wide-based gait resulting from damage to the cerebellum, impairing the integration of proprioceptive and vestibular input.

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Beta-Blockers (β1\beta_1 antagonists)

Drugs that lower heart rate and blood pressure; non-selective versions can cause bronchoconstriction via β2\beta_2 blockade.

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Atropine

A competitive antagonist of muscarinic ACh receptors used to treat bradycardia and serve as an antidote for organophosphate poisoning.

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Autonomic Dysreflexia

A condition occurring in spinal cord injuries at or above T6 where a noxious stimulus below the lesion triggers massive, uninhibited sympathetic vasoconstriction.

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Pneumothorax

A condition where air breaches the intrapleural space, causing the loss of negative transmural pressure and resulting in lung collapse.

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Neonatal Respiratory Distress Syndrome (RDS)

A lack of surfactant produced by Type II alveolar cells which increases alveolar surface tension and leads to diffuse atelectasis.

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Pulse Oximetry

A diagnostic method emitting 660nm660\,nm red and 940nm940\,nm infrared light to measure the absorption ratios of Oxy-Hb vs. Deoxy-Hb.

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Carbon Monoxide (CO) Poisoning

CO binds hemoglobin with more than 200×200\times higher affinity than O2O_2, forming carboxyhemoglobin (CO-Hb) and preventing O2O_2 unloading to tissues.

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Ondine's Curse (CCHS)

A mutation in the retrotrapezoid nucleus of the medulla oblongata that abolishes the automatic respiratory response to elevated arterial $P_{CO_2}$.

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Respiratory Alkalosis via Hyperventilation

A high blood pH caused by excessive "blowing off" of CO2CO_2, which lowers ionized plasma Ca2+Ca^{2+} and causes neuromuscular tetany.

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Barrett's Esophagus

Metaplasia where esophageal stratified squamous epithelium is replaced by acid-resistant simple columnar epithelium due to chronic GERD.

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Proton Pump Inhibitors (PPIs)

Drugs used to treat GERD by inhibiting the parietal cell H+/K+H^+/K^+ ATPase pumps.

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Lactose Intolerance

A deficiency of the brush border lactase enzyme, leading to undigested lactose exerting osmotic force and causing diarrhea.

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Celiac Disease

An autoimmune reaction to gluten that destroys duodenal and jejunal villi, flattening the surface area and causing severe malabsorption.

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Crohn's Disease

A type of inflammatory bowel disease characterized by transmural inflammation and fibrotic skip lesions throughout the GI tract.

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Ulcerative Colitis

Inflammatory bowel disease involving mucosal and submucosal erosion that starts in the rectum and progresses proximally through the colon.

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Liver Cirrhosis

The replacement of hepatic lobules with non-functional fibrotic scar tissue, leading to portal hypertension and impaired toxin clearance.

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Pre-hepatic Jaundice

Yellowing of tissues caused by excessive hemolysis (e.g., Sickle Cell) which overwhelms the liver's conjugation capacity.

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Post-hepatic Jaundice

Jaundice caused by biliary tree obstruction, such as gallstones, which blocks bile drainage into the duodenum.

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Cytochrome P450 (CYP3A4) and Grapefruit

Grapefruit juice inhibits this enzyme in hepatocytes, slowing drug breakdown and causing toxic accumulation in plasma.

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Pancreatitis Pathophysiology

The premature intracellular activation of pancreatic zymogens (e.g., trypsinogen to trypsin) causing enzymatic auto-digestion of pancreatic tissue.