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Role of the Nrf2 Signaling Pathway in Ovarian Aging: Potential Mechanism and Protective Strategies

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MDPI
DOI: 10.3390/ijms241713327

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ovarian aging; oxidative stress; Nrf2; antioxidant therapy

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The ovary, as a reproductive endocrine organ in women, plays a significant role in the aging process, leading to menopause, decreased fertility, and long-term health risks. Oxidative stress is closely associated with aging metabolic processes and affects both physiological and pathological ovarian aging. The Nrf2 pathway is crucial in regulating the antioxidant response, and therapeutic strategies aimed at modulating this pathway have been identified to ameliorate ovarian aging.
The ovary holds a significant role as a reproductive endocrine organ in women, and its aging process bears implications such as menopause, decreased fertility, and long-term health risks including osteoporosis, cardiovascular disorders, and cognitive decline. The phenomenon of oxidative stress is tightly linked to the aging metabolic processes. More and more studies have demonstrated that oxidative stress impacts both physiologic and pathologic ovarian aging, and the nuclear factor erythroid 2-related factor 2 (Nrf2) pathway plays a crucial role in regulating the antioxidant response. Furthermore, various therapeutic approaches have been identified to ameliorate ovarian aging by modulating the Nrf2 pathway. This review summarizes the important role of the Nrf2/ Kelch-like ECH-associated protein 1 (Keap1) signaling pathway in regulating oxidative stress and influencing ovarian aging. Additionally, it highlights the therapeutic strategies aimed at targeting the Nrf2/Keap1 pathway.

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