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Chapter 4

Pharmacodynamics

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약물 작용의 원칙
약물 작용의 원칙
Drugs are chemical substances that modify biological responses by interacting with macromolecular targets such as receptors, ion channels, transporters, ...

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약물 작용의 목표: 개요
약물 작용의 목표: 개요
Drugs target macromolecules to modify ongoing cellular processes. Primary drug targets include receptors, ion channels, transporters, and enzymes. ...

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신호 전달: 개요
신호 전달: 개요
Cells respond to many types of information, often through receptor proteins positioned on the membrane. They respond to chemical signals, such as ...

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변환기 메커니즘: G 단백질 결합 수용체
변환기 메커니즘: G 단백질 결합 수용체
G Protein–Coupled Receptors (GPCRs) are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate ...

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리간드 게이트 이온 채널 수용체: 게이팅 메커니즘
리간드 게이트 이온 채널 수용체: 게이팅 메커니즘
Ligand-gated ion channels are transmembrane proteins that play a vital role in intercellular communication and functions of the nervous system. They allow ...

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변환기 메커니즘: 효소 결합 수용체
변환기 메커니즘: 효소 결합 수용체
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. ...

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트랜스듀서 메커니즘: 핵 수용체
트랜스듀서 메커니즘: 핵 수용체
Nuclear receptors, or NRs, are unique transcription factors that regulate gene transcription and affect the cellular pathways involved in reproduction, ...

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용량-반응 관계: 개요
용량-반응 관계: 개요
Agonists can bind with and activate receptors, resulting in the formation of drug-receptor complexes. Once formed, these complexes catalyze many ...

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용량-반응 관계: 효능 및 효능
용량-반응 관계: 효능 및 효능
The potency of a drug is the measure of its ability to produce a biological response and can be compared by looking at the half-maximum effective ...

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용량-반응 관계: 선택성 및 특이성
용량-반응 관계: 선택성 및 특이성
Drugs exert their therapeutic effects by interacting with receptors, enzymes, or ion channels that are present throughout the human body. The strength and ...

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치료 지수
치료 지수
The therapeutic index of a drug is a key parameter in pharmacology that quantifies the relative safety of a drug by calculating the ratio between the dose ...

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약물-수용체 상호작용: 작용제
약물-수용체 상호작용: 작용제
Agonists are drugs that interact with specific receptors in the body to produce a biological response. When an agonist binds to a receptor, it activates ...

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약물-수용체 상호 작용: 길항제
약물-수용체 상호 작용: 길항제
An antagonist is a drug that binds strongly to a receptor without activating it. An antagonist prevents other molecules, such as neurotransmitters or ...

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약물의 복합 효과: 길항작용
약물의 복합 효과: 길항작용
The combined effects of drugs can result in various interactions, of which an important type is antagonism. Antagonism is a mechanism where one drug ...

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약물의 복합 효과: 시너지 효과
약물의 복합 효과: 시너지 효과
Synergism is a useful mechanism where combining two or more drugs is more effective than each constituent used alone. Such combinations are also called ...

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예비 수용체
예비 수용체
Some receptors remain unoccupied even when an agonist produces a maximal response. Such empty ones are called spare receptors. In presence of spare ...

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약물-수용체 상호작용의 정량적 측면
약물-수용체 상호작용의 정량적 측면
The receptor occupancy theory connects a drug's response to the number of occupied receptors. With higher drug concentrations, more receptors are ...

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두 상태 수용체 모델
두 상태 수용체 모델
The two-state receptor model explains a drug's interaction with receptors, such as G protein-coupled receptors and ligand-gated ion channels, to ...

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둔감화(Desensitization)와 타키필락시스(Tachyphylaxis)
둔감화(Desensitization)와 타키필락시스(Tachyphylaxis)
Tachyphylaxis is described as a rapid decrease in response to a drug after repeated or continuous administration of the same drug dose. It is a phenomenon ...
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