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Thymulin is a zinc-dependent nonapeptide hormone that regulates T-cell development, immune function, and neuroendocrine signaling. Its role in inflammation, analgesia, and immune aging makes it a versatile tool in immunology and neurobiology research. Synthetic analogs extend its utility in exploring CNS and inflammatory pathways.
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Thymulin is a zinc-dependent nonapeptide hormone (H-Pyr-Ala-Lys-Ser-Gln-Gly-Gly-Ser-Asn-OH) secreted by thymic epithelial cells. It supports T-cell differentiation, modulates immune and neuroendocrine signaling, exhibits anti-inflammatory and analgesic properties, and interacts with the hypothalamus–pituitary axis in research contexts.[1]
Thymulin is widely used to study immune system development, thymic function, and age-related immunosenescence. It provides a reliable model for exploring T-cell maturation and thymic decline.[4]
Its circadian secretion pattern and bidirectional influence on the hypothalamus–pituitary axis make thymulin central to neuroimmunology research.[5]
Thymulin and PAT exhibit potent analgesic and anti-inflammatory effects in CNS research, often surpassing conventional drugs in potency at low doses. They act by reducing cytokine expression and restoring astrocyte balance via NF-κB modulation.[6]
Reduced circulating thymulin has been documented in conditions such as anorexia nervosa and thymic involution with aging, positioning it as a biomarker in immunology and aging studies.[7]
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