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The Two-State Receptor Model01:29

The Two-State Receptor Model

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The two-state receptor model explains a drug's interaction with receptors, such as G protein-coupled receptors and ligand-gated ion channels, to induce or inhibit a biological response. When no natural ligands are present, a receptor exists in an equilibrium of inactive (Ri) and active (Ra) conformations. The inactive form does not produce a response, while the active form generates a basal effect known as constitutive activity.
The binding affinity of a drug determines its interaction with...
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Target Cell Response to Hormones01:22

Target Cell Response to Hormones

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Hormones intricately bind to receptors on the surface or within target cells, initiating a cascade of cellular responses.
Notably, the cellular response can be regulated by altering the number of receptors expressed in the cell. For example, prolonged exposure to elevated hormone levels results in a gradual decline or down-regulation in the number of receptors for that specific hormone on the cell surface. Conversely, in response to low hormone levels, cells may use up-regulation, producing an...
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Transduction01:16

Transduction

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Among the three main modes of HGT—transformation, conjugation, and transduction—transduction is unique in that it is mediated by bacteriophages, or bacterial viruses.Transduction occurs in two ways. Generalized transduction occurs during the lytic cycle of a bacteriophage infection. In this process, bacteriophages infect bacterial cells, replicate within them, and ultimately cause cell lysis, releasing newly assembled virions. Occasionally, random fragments of the bacterial genome...
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Secondary Messengers in Hormone Action01:26

Secondary Messengers in Hormone Action

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Water-soluble hormones cannot cross the plasma membrane, so they rely on protein receptors that span the membrane to trigger intracellular signaling pathways. These pathways then activate second messengers inside the cell, including cAMP or calcium ions.
Many hormones bind to transmembrane G protein-coupled receptors that connect to regulatory G proteins. These G proteins can then activate enzymes such as adenylyl cyclase or phospholipase C. Adenylyl cyclase converts ATP to cAMP, activating...
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Chemical Signaling in the Endocrine System01:08

Chemical Signaling in the Endocrine System

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A signaling cascade is a series of events that facilitates the transmission of information within or between cells, culminating in a targeted response in the recipient cell. As chemical messengers, hormones are pivotal in initiating and modulating these intricate signaling cascades based on their solubility.
Lipid-soluble hormones, such as steroid hormones, demonstrate an intracellular action. These hormones traverse cell membranes due to their lipid nature. Once inside the target cell, they...
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Hormonal Regulation01:33

Hormonal Regulation

37.0K
The renin-aldosterone system is an endocrine system which guides the renal absorption of water and electrolytes, thus managing blood pressure and osmoregulation. Activation of the system begins in the kidneys with a small cluster of cells adjacent to the afferent and efferent blood vessels of the renal corpuscle. As the nephrons are filtering blood, juxtaglomerular cells monitor blood pressure. If they detect a decrease in pressure, they release the hormone renin into the bloodstream.
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Related Experiment Video

Updated: Mar 28, 2026

Quantification of Information Encoded by Gene Expression Levels During Lifespan Modulation Under Broad-range Dietary Restriction in C. elegans
09:23

Quantification of Information Encoded by Gene Expression Levels During Lifespan Modulation Under Broad-range Dietary Restriction in C. elegans

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Hormesis: Decoding Two Sides of the Same Coin.

Dipita Bhakta-Guha1, Thomas Efferth2

  • 1School of Chemical and Biotechnology, SASTRA University, Thanjavur, Tamil Nadu 613401, India. dipita2001@gmail.com.

Pharmaceuticals (Basel, Switzerland)
|December 24, 2015
PubMed
Summary
This summary is machine-generated.

Hormesis describes how substances can have opposite effects at high and low doses. Understanding this biphasic effect is crucial for drug administration and cancer research, impacting disease progression and treatment strategies.

Keywords:
biphasiccancerhormesismimeticspathwaysstressor

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Area of Science:

  • Pharmacology and Toxicology
  • Molecular Biology
  • Oncology

Background:

  • Drug dosage is critical, as some therapeutics exhibit opposing effects at high versus low concentrations.
  • This dose-dependent duality is termed hormesis, necessitating study for mechanistic understanding.
  • Hormesis plays a significant role in various disease pathways, including cancer progression.

Purpose of the Study:

  • To explore molecules and pathways exhibiting hormetic (biphasic) effects.
  • To specifically analyze how hormesis influences cancer progression through key molecular pathways.
  • To highlight the importance of understanding hormesis in disease and stress response.

Main Methods:

  • Review of scientific literature on hormesis and its molecular basis.
  • Analysis of key signaling pathways involved in cancer, such as Nrf2-Keap1 and SIRT-FOXO.
  • Examination of how molecular concentration affects pathway activity and disease manifestation.

Main Results:

  • Identified diverse molecules and pathways that demonstrate hormetic behavior.
  • Detailed how the biphasic action of molecules in pathways like Nrf2-Keap1 and SIRT-FOXO can alter cancer progression.
  • Highlighted the role of stressors in triggering hormesis and enhancing adaptive responses.

Conclusions:

  • Hormesis is a critical concept in understanding drug efficacy and disease mechanisms.
  • The biphasic nature of molecules in key cancer pathways offers new insights into disease management.
  • Further research into hormesis is essential for developing targeted therapeutic strategies.