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第4章

薬力学

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薬物作用の原則
薬物作用の原則
Drugs are chemical substances that modify biological responses by interacting with macromolecular targets such as receptors, ion channels, transporters, ...

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薬物作用の標的:概要
薬物作用の標的:概要
Drugs target macromolecules to modify ongoing cellular processes. Primary drug targets include receptors, ion channels, transporters, and enzymes. ...

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シグナル伝達:概要
シグナル伝達:概要
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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トランスデューサーメカニズム:Gタンパク質共役受容体
トランスデューサーメカニズム:Gタンパク質共役受容体
G Protein–Coupled Receptors (GPCRs) are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate ...

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リガンド依存性イオンチャネル受容体:ゲーティング機構
リガンド依存性イオンチャネル受容体:ゲーティング機構
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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トランスデューサーメカニズム:酵素結合受容体
トランスデューサーメカニズム:酵素結合受容体
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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トランスデューサーメカニズム:核内受容体
トランスデューサーメカニズム:核内受容体
Nuclear receptors, or NRs, are unique transcription factors that regulate gene transcription and affect the cellular pathways involved in reproduction, ...

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用量反応関係:概要
用量反応関係:概要
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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用量反応関係:効力と効能
用量反応関係:効力と効能
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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用量反応関係:選択性と特異性
用量反応関係:選択性と特異性
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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治療指数
治療指数
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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薬物-受容体相互作用:アゴニスト
薬物-受容体相互作用:アゴニスト
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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薬物-受容体相互作用:アンタゴニスト
薬物-受容体相互作用:アンタゴニスト
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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薬物の複合効果:拮抗作用
薬物の複合効果:拮抗作用
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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薬物の複合効果:シナジー
薬物の複合効果:シナジー
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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スペア受容体
スペア受容体
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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薬物-受容体相互作用の量的側面
薬物-受容体相互作用の量的側面
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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2状態受容体モデル
2状態受容体モデル
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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脱感作とタキフィラキシー
脱感作とタキフィラキシー
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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