Arachidonyl-2'-chloroethylamide

Also called ACEA

Arachidonyl-2'-chloroethylamide has been studied in 3 papers since 2016: none in people yet, 1 in animals, 2 in cells. The research so far is in animals and cells. The newest paper, Aug 25, 2023: “Cannabinoid receptor type 1 in the aging gut regulates the mucosal permeability via miR-191-5p”.

Intervention

3 papers study it4 findingsUpdated

PubChemChEBIMeSH

See all 3 papers on arachidonyl-2'-chloroethylamide

At a glance

The findings reach cells, none yet in people. 2 independent labs in 2 countries.

None of its findings points the other way.

Cells: a single group. Worms or flies, mice and humans: nothing yet.
  • 2 independent labs in 2 countries
  • Funders: National Natural Science Foundation of China and 3 more
  • Animals1
  • Cells2

What did studies of arachidonyl-2'-chloroethylamide find?

4

Studies of arachidonyl-2'-chloroethylamide measured 4 outcomes, among them MIR191, SIRT1 and senescence gene expression.

MIR191

downin rat cells1

1 study
  1. Arachidonyl-2'-chloroethylamide decreases MIR191 in HU-induced senescent cells.

    “Increased expression of miR-191-5p by HU was restored by CB1 agonist ACEA co-treatment.”

    Cellsin HU-induced senescent cells

    Cannabinoid receptor type 1 in the aging gut regulates the mucosal permeability via miR-191-5p

    Frontiers in endocrinology

More on MIR191

SIRT1

upin human cells1

1 study
  1. Arachidonyl-2'-chloroethylamide increases SIRT1 in human cells.

    “agonist arachidonyl-2-chloroethylamide enhanced the expression of sirt1.”

    Cells

    Activation of the cannabinoid receptor 1 by ACEA suppresses senescence in human primary chondrocytes through sirt1 activation

    Experimental biology and medicine (Maywood, N.J.)

More on SIRT1

Senescence gene expression

downin human cells1

1 study
  1. Arachidonyl-2'-chloroethylamide decreases senescence gene expression in interleukin-1β-treated chondrocytes.

    “interleukin-1βtreatment significantly increased the expressions of senescence genes (caveolin-1, PAI-1 and p21), which were prevented by agonist arachidonyl-2-chloroethylamide treatment.”

    Cellsin interleukin-1β-treated chondrocytes

    Activation of the cannabinoid receptor 1 by ACEA suppresses senescence in human primary chondrocytes through sirt1 activation

    Experimental biology and medicine (Maywood, N.J.)

More on Senescence gene expression

Cellular senescence

downin human cells1

1 study
  1. Arachidonyl-2'-chloroethylamide decreases cellular senescence in interleukin-1β-induced senescence.

    “Our findings demonstrate that agonist arachidonyl-2-chloroethylamidedecreased senescence-associated β-galactosidase activity and cell cycle arrest in the G0/G1 phase induced by interleukin-1β.”

    Cellsin interleukin-1β-induced senescence

    Activation of the cannabinoid receptor 1 by ACEA suppresses senescence in human primary chondrocytes through sirt1 activation

    Experimental biology and medicine (Maywood, N.J.)

More on Cellular senescence

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