Component

CB1 receptor desensitisation

CB1 receptor desensitisation. Species, exposure and limitations are retained in each linked claim.

2 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What it acts on

  1. Rapid CB1 receptor desensitisation defines the time course of ERK1/2 MAP kinase signalling.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    evidence_span
    {"source_cache": "artifacts/thc-research/17681354.abstract.txt", "locator": "Indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "dda88f2600ad5892232cf931091df54c5fc62b303062f725df663d65778c4821", "start_char": 0, "end_char": 1915, "text_sha256": "dda88f2600ad5892232cf931091df54c5fc62b303062f725df663d65778c4821"}
    experimental_model
    Time-course measurement of CB1 desensitisation against ERK signalling
    exposure
    Agonist exposure with kinase and receptor measurement
    limitations
    Ties the adaptation timescale to a downstream kinase, which is what makes desensitisation measurable as a signalling change rather than only as binding.
    nutrient_topic
    THC research collection; topical membership is not evidence of a direct clinical effect, and THC is recorded separately from the endocannabinoids it imitates. · Delta-9-tetrahydrocannabinol / THC
    organism
    Cultured cells
    plain_language
    How fast the receptor goes deaf sets how long the downstream signal lasts.
    primary_references
    [thc-p17681354] Rapid CB1 cannabinoid receptor desensitization defines the time course of ERK1/2 MAP kinase signaling. (2008). https://pubmed.ncbi.nlm.nih.gov/17681354/ DOI: 10.1016/j.neuropharm.2007.06.005
    tissue_or_cell_type
    Transfected cells
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    THC: the cannabinoid receptors, the endocannabinoid system it occupies, what the drug does, and the dietary fat it is built from (2026-09-21) · lines 218–229

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Time-course measurement of CB1 desensitisation against ERK signalling · source_derived_draft · unverified_draft

    ### thc-desensitisation-erk Rapid CB1 receptor desensitisation defines the time course of ERK1/2 MAP kinase signalling. Condition category: machinery_impairment nutrient_topic: THC research collection; topical membership is not evidence of a direct clinical effect, and THC is recorded separately from the endocannabinoids it imitates. plain_language: How fast the receptor goes deaf sets how long the downstream signal lasts. organism: Cultured cells tissue_or_cell_type: Transfected cells experimental_model: Time-course measurement of CB1 desensitisation against ERK signalling limitations: Ties the adaptation timescale to a downstream kinase, which is what makes desensitisation measurable as a signalling change rather than only as binding. exposure: Agonist exposure with kinase and receptor measurement evidence_span: {"source_cache": "artifacts/thc-research/17681354.abstract.txt", "locator": "Indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "dda88f2600ad5892232cf931091df54c5fc62b303062f725df663d65778c4821", "start_char": 0, "end_char": 1915, "text_sha256": "dda88f2600ad5892232cf931091df54c5fc62b303062f725df663d65778c4821"} [thc-p17681354] Rapid CB1 cannabinoid receptor desensitization defines the time course of ERK1/2 MAP kinase signaling. (2008). https://pubmed.ncbi.nlm.nih.gov/17681354/ DOI: 10.1016/j.neuropharm.2007.06.005
    Complete structured claim and evidence

What acts on it

  1. Distinct domains of the CB1 receptor mediate desensitisation and internalisation, so the two adaptive responses are separable.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    evidence_span
    {"source_cache": "artifacts/thc-research/10234009.abstract.txt", "locator": "Indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "73965589817407e173255ab6db300e7969b0e91a4ca4cd3d39cee1f5873d1e05", "start_char": 0, "end_char": 1911, "text_sha256": "73965589817407e173255ab6db300e7969b0e91a4ca4cd3d39cee1f5873d1e05"}
    experimental_model
    Mutational mapping of CB1 receptor domains against desensitisation and internalisation
    exposure
    Sustained agonist exposure with receptor trafficking measurement
    limitations
    Separates two adaptive processes that are often conflated. It is a recombinant system.
    nutrient_topic
    THC research collection; topical membership is not evidence of a direct clinical effect, and THC is recorded separately from the endocannabinoids it imitates. · Delta-9-tetrahydrocannabinol / THC
    organism
    Recombinant receptor
    plain_language
    Going deaf to the drug and removing the receptor from the surface are two different things.
    primary_references
    [thc-p10234009] Distinct domains of the CB1 cannabinoid receptor mediate desensitization and internalization. (1999). https://pubmed.ncbi.nlm.nih.gov/10234009/ DOI: 10.1523/jneurosci.19-10-03773.1999
    tissue_or_cell_type
    Transfected cells
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    THC: the cannabinoid receptors, the endocannabinoid system it occupies, what the drug does, and the dietary fat it is built from (2026-09-21) · lines 205–216

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Mutational mapping of CB1 receptor domains against desensitisation and internalisation · source_derived_draft · unverified_draft

    ### thc-desensitisation-domains Distinct domains of the CB1 receptor mediate desensitisation and internalisation, so the two adaptive responses are separable. Condition category: machinery_impairment nutrient_topic: THC research collection; topical membership is not evidence of a direct clinical effect, and THC is recorded separately from the endocannabinoids it imitates. plain_language: Going deaf to the drug and removing the receptor from the surface are two different things. organism: Recombinant receptor tissue_or_cell_type: Transfected cells experimental_model: Mutational mapping of CB1 receptor domains against desensitisation and internalisation limitations: Separates two adaptive processes that are often conflated. It is a recombinant system. exposure: Sustained agonist exposure with receptor trafficking measurement evidence_span: {"source_cache": "artifacts/thc-research/10234009.abstract.txt", "locator": "Indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "73965589817407e173255ab6db300e7969b0e91a4ca4cd3d39cee1f5873d1e05", "start_char": 0, "end_char": 1911, "text_sha256": "73965589817407e173255ab6db300e7969b0e91a4ca4cd3d39cee1f5873d1e05"} [thc-p10234009] Distinct domains of the CB1 cannabinoid receptor mediate desensitization and internalization. (1999). https://pubmed.ncbi.nlm.nih.gov/10234009/ DOI: 10.1523/jneurosci.19-10-03773.1999
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards