Pharmacology 2 (Lecture) - Cardiovascular System and Blood Pressure

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Vocabulary-style flashcards covering cardiovascular pharmacology, receptor mechanisms, hemodynamics, and hypertension based on the course outline and lecture notes.

Last updated 11:58 AM on 8/18/26
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41 Terms

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CO1

A course outcome to describe principles of pharmacology, pharmacokinetics, and pharmacodynamics for drugs acting on central, autonomic, respiratory, and gastrointestinal systems.

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Systemic circulatory system

The main blood circulatory system that transports blood to the organs, tissues, and cells throughout the body.

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Pulmonary circulatory system

The circulatory system that moves blood between the heart and lungs, facilitating oxygen entry and carbon dioxide removal.

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Tricuspid Valve

The valve located between the right atrium and the right ventricle path.

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Mitral Valve

The valve located between the left atrium and the left ventricle path.

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S1S_1

Normal heart sound originating from the closing of the atrioventricular valves; high-pitched, heard with a diaphragm.

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S2S_2

Normal heart sound originating from the closing of the semilunar valves; high-pitched, heard with a diaphragm.

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S3S_3

Heart sound potentially indicating fluid overload or failure; low-pitched, heard with a bell.

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S4S_4

Abnormal heart sound indicating ventricle resistance; low-pitched, heard with a bell.

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Murmurs

Low-pitched sounds that may indicate a wall defect or valve problem, heard with a bell.

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Cardiac Output (COCO)

The volume of blood ejected per minute, calculated as SV×HRSV \times HR.

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Stroke Volume (SVSV)

The volume of blood ejected in each heartbeat.

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Peripheral Resistance (PRPR)

Also known as Systemic Vascular Resistance (SVRSVR); the resistance the left ventricle must overcome to pump blood to the body.

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Blood Pressure formula

BP=CardiacOutput×PeripheralResistanceBP = Cardiac Output \times Peripheral Resistance (CO×PRCO \times PR).

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Troponin

The protein that binds calcium to move tropomyosin, allowing muscle contraction in the heart.

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Ligand-Gated Ion Channel

Also called ionotropic; an ion channel that opens/closes in milliseconds when a ligand binds (e.g., Nicotinic ACh).

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G Protein-Coupled Receptor (GPCR)

Receptors that activate G proteins (Gs, Gi, Gq) and second messengers, responding within seconds (e.g., α\alpha and β\beta receptors).

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Enzyme-Linked Receptor

A receptor with intrinsic enzyme activity, such as tyrosine kinase, responding in minutes to hours (e.g., Insulin receptor).

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Intracellular Receptor

Receptors located in the nucleus or cytoplasm where the ligand enters the cell to alter gene transcription; responds in hours to days.

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GsG_s (G stimulatory)

A G protein subtype that increases cAMPcAMP (e.g., β1\beta_1, β2\beta_2, β3\beta_3, D1D_1, H2H_2, V2V_2).

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GiG_i (G inhibitory)

A G protein subtype that decreases cAMPcAMP (e.g., α2\alpha_2, M2M_2, D2D_2).

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GqG_q

A G protein subtype that activates phospholipase C (PLCPLC), increasing IP3IP_3, DAGDAG, and Ca2+Ca^{2+} (e.g., α1\alpha_1, M1M_1, M3M_3, H1H_1, V1V_1).

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IP3IP_3

A second messenger in the cytoplasm that opens Ca2+Ca^{2+} channels on the sarcoplasmic reticulum.

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DAGDAG

A second messenger in the cell membrane that activates Protein Kinase C (PKCPKC).

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β1\beta_1 Receptor

The dominant sympathetic receptor in the heart that increases heart rate (positive chronotropy) and force (positive inotropy).

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M2M_2 Receptor

The dominant parasympathetic receptor in the heart that decreases heart rate and atrial contractility.

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Dobutamine

A β1\beta_1 agonist used to increase heart rate and contractility.

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Metoprolol

A β1\beta_1 blocker used to decrease heart rate and contractility.

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Atropine

An M2M_2 antagonist that increases heart rate by blocking vagal effects.

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Low-dose Dopamine

Dosage of 13mcg/kg/min1\text{--}3\,mcg/kg/min that primarily acts on D1D_1 receptors for renal and mesenteric vasodilation.

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Moderate-dose Dopamine

Dosage of 310mcg/kg/min3\text{--}10\,mcg/kg/min that primarily acts on β1\beta_1 receptors to increase cardiac output.

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High-dose Dopamine

Dosage of >10mcg/kg/min>10\,mcg/kg/min that primarily acts on α1\alpha_1 receptors for vasoconstriction and increased blood pressure.

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Phenylephrine

An α1\alpha_1 agonist that causes strong arterial and venous constriction.

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Nitroglycerin

A drug that primarily causes marked venodilation and mild arterial dilation.

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Renin

Enzyme released from the kidney in response to low blood pressure that acts on angiotensinogen.

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Angiotensin II

A powerful vasoconstrictor formed by ACE that stimulates aldosterone and vasopressin secretion.

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Aldosterone

A hormone from the adrenal gland that stimulates the kidneys to reabsorb salt (NaClNaCl) and water (H2OH_2O).

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Atrial Natriuretic Peptide (ANP)

Hormone that reduces blood volume and blood pressure by increasing sodium and water excretion.

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Preload

The amount of blood in the ventricles at the end of diastole.

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Stage 1 Hypertension

A blood pressure category with systolic 130139mmHg130\text{--}139\,mm\,Hg or diastolic 8089mmHg80\text{--}89\,mm\,Hg.

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Hypertensive crisis

Clinical urgency with systolic above 180mmHg180\,mm\,Hg and/or diastolic above 120mmHg120\,mm\,Hg.