TAT-HSP10

TAT-HSP10 has been studied in 1 paper since 2023: none in people yet, 1 in animals. The research so far is in animals. The newest paper, Nov 25, 2023: “Tat-heat shock protein 10 ameliorates age-related phenotypes by facilitating neuronal plasticity and reducing age-related genes in the hippocampus”.

Intervention

1 paper studies it3 findingsUpdated

None of its findings points the other way.

  • 1 lab in 1 country
  • Funders: Ministry of Science and ICT, South Korea and 4 more
  • Animals1

What did studies of TAT-HSP10 find?

3

Studies of TAT-HSP10 measured 3 outcomes; the most studied are stem cell differentiation (1 study), cognitive function (1) and cellular senescence (1).

Stem cell differentiation

upin mice1

1 study
  1. TAT-HSP10 increases stem cell differentiation in mice.

    “Administration of Tat-HSP10 increased the number of proliferating cells and differentiated neuroblasts in the dentate gyrus of adult and aged mice compared to controls”

    Animalsdentate gyrus0.5 or 2.0 mg/kg3 months

    Tat-heat shock protein 10 ameliorates age-related phenotypes by facilitating neuronal plasticity and reducing age-related genes in the hippocampus

    Aging

More on Stem cell differentiation

Cognitive function

upin mice1

1 study
  1. TAT-HSP10 improves cognitive function in mice.

    “Treatment with Tat-HSP10 significantly improved exploratory preferences, the number of object contacts, and the time spent swimming in the target quadrant in aged mice”

    Animals0.5 or 2.0 mg/kg3 months

    Tat-heat shock protein 10 ameliorates age-related phenotypes by facilitating neuronal plasticity and reducing age-related genes in the hippocampus

    Aging

Cellular senescence

downin mice1

1 study
  1. TAT-HSP10 decreases cellular senescence in mice.

    “treatment with Tat-HSP10 significantly decreased P16 expression in the hippocampus of aged mice.”

    Animalshippocampus0.5 or 2.0 mg/kg3 months

    Tat-heat shock protein 10 ameliorates age-related phenotypes by facilitating neuronal plasticity and reducing age-related genes in the hippocampus

    Aging

More on Cellular senescence

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