Mitochondria-targeted senotherapeutic interventions


Atayik M. C., ÇAKATAY U.

BIOGERONTOLOGY, cilt.23, sa.4, ss.401-423, 2022 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Derleme
  • Cilt numarası: 23 Sayı: 4
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1007/s10522-022-09973-y
  • Dergi Adı: BIOGERONTOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Abstracts in Social Gerontology, BIOSIS, EMBASE, MEDLINE
  • Sayfa Sayıları: ss.401-423
  • Anahtar Kelimeler: Aging, Mitochondria, Senescence, Senotherapeutics, CELLULAR SENESCENCE, OXIDATIVE STRESS, SMALL-MOLECULE, HEART-FAILURE, S-NITROSATION, DELIVERY, DRUG, DYSFUNCTION, MECHANISMS, PROTECTS
  • İstanbul Üniversitesi Adresli: Hayır

Özet

Healthy aging is the art of balancing a delicate scale. On one side of the scale, there are the factors that make life difficult with aging, and on the other side are the products of human effort against these factors. The most important factors that make the life difficult with aging are age-related disorders. Developing senotherapeutic strategies may bring effective solutions for the sufferers of age-related disorders. Mitochondrial dysfunction comes first in elucidating the pathogenesis of age-related disorders and presenting appropriate treatment options. Although it has been widely accepted that mitochondrial dysfunction is a common characteristic of cellular senescence, it still remains unclear why dysfunctional mitochondria occupy a central position in the development senescence-associated secretory phenotype (SASP) related to age-related disorders. Mitochondrial dysfunction and SASP-related disease progression are closely interlinked to weaken immunity which is a common phenomenon in aging. A group of substances known as senotherapeutics targeted to senescent cells can be classified into two main groups: senolytics (kill senescent cells) and senomorphics/senostatics (suppress their SASP secretions) in order to extend health lifespan and potentially lifespan. As mitochondria are also closely related to the survival of senescent cells, using either mitochondria-targeted senolytic or redox modulator senomorphic strategies may help us to solve the complex problems with the detrimental consequences of cellular senescence. Killing of senescent cells and/or ameliorate their SASP-related negative effects are currently considered to be effective mitochondria-directed gerotherapeutic approaches for fighting against age-related disorders.