Strain-specificity in the hydrogen sulphide signalling network following dietary restriction in recombinant inbred mice

Modulation of the ageing process by dietary restriction (DR) across multiple taxa is well established. While the exact mechanism through which DR acts remains elusive, the gasotransmitter hydrogen sulphide (H(2)S) may play an important role. We employed a comparative-type approach using females from three ILSXISS recombinant inbred mouse strains previously reported to show differential lifespan responses following 40% DR. Following long-term (10 months) 40% DR, strain TejJ89—reported to show lifespan extension under DR—exhibited elevated hepatic H(2)S production relative to its strain-specific ad libitum (AL) control. Strain TejJ48 (no reported lifespan effect following 40% DR) exhibited significantly reduced hepatic H(2)S production, while H(2)S production was unaffected by DR in strain TejJ114 (shortened lifespan reported following 40% DR). These differences in H(2)S production were reflected in highly divergent gene and protein expression profiles of the major H(2)S production and disposal enzymes across strains. Increased hepatic H(2)S production in TejJ89 mice was associated with elevation of the mitochondrial H(2)S-producing enzyme 3-mercaptopyruvate sulfurtransferase (MPST). Our findings further support the potential role of H(2)S in DR-induced longevity and indicate the presence of genotypic-specificity in the production and disposal of hepatic H(2)S in response to 40% DR in mice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11357-020-00168-2) contains supplementary material, which is available to authorized users.