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About Biomedical Basics
Biomedical Basics are AI-generated explanations prepared with access to the complete collection, human-reviewed prior to publication. Short and simple, covering biomedical and life sciences fundamentals.
Topics Covered
- Hormonal regulation of metabolism
- Major metabolic hormones
- Hormone action mechanisms
- Hormonal control of macronutrient metabolism
- Hormonal imbalances in metabolic diseases
Links
Categories:
Therapeutic Areas:
Talk Citation
(2025, November 30). Hormonal regulation of metabolism [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 4, 2025, from https://doi.org/10.69645/BTOL7028.Export Citation (RIS)
Publication History
- Published on November 30, 2025
Financial Disclosures
A selection of talks on Metabolism & Nutrition
Transcript
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0:00
This talk introduces hormonal
regulation of metabolism,
using it as a basis for
further exploration of the
hormonal regulation
of metabolism,
emphasizing the key roles of
insulin, glucagon,
thyroid hormones,
cortisol, growth hormone,
and epinephrine in maintaining
energy balance and homeostasis.
We will examine
how these hormones
control carbohydrate, fat,
and protein metabolism through
specific signaling pathways
and feedback mechanisms.
Lecture will also discuss
how imbalances in
these hormones lead to
metabolic diseases
such as diabetes,
thyroid disorders, and
Cushing's syndrome,
underscoring the
clinical importance
of endocrine regulation.
Metabolism is under
precise hormonal control,
enabling the body to
adapt to changing
nutritional states and
environmental demands.
Hormones like insulin,
glucagon, thyroid
hormones, cortisol,
growth hormone, and
epinephrine act as
chemical messengers orchestrating
metabolic pathways.
They regulate energy
production and
the synthesis and breakdown
of carbohydrates, fats,
and proteins via
mechanisms such as
G-protein coupled and
nuclear receptors
ensuring homeostasis.
Insulin and glucagon are
the main hormones
regulating blood sugar.
Insulin from pancreatic
beta cells in response
to high glucose promotes
tissue glucose uptake,
glycogen synthesis,
glycolysis and
lipogenesis while
inhibiting gluconeogenesis
and lipolysis.
It acts via tyrosine
kinase receptors