4.7 Article

Hydrogen Sulfide Inhibited Sympathetic Activation in D-Galactose-Induced Aging Rats by Upregulating Klotho and Inhibiting Inflammation in the Paraventricular Nucleus

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BIOMEDICINES
卷 11, 期 2, 页码 -

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MDPI
DOI: 10.3390/biomedicines11020566

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hydrogen sulfide; sympathetic excitation; paraventricular nucleus; aging; klotho; inflammation

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The present study explored the relationship between cardiovascular conditions and aging. D-galactose (D-gal) was used to induce an accelerated aging model and evaluate the effects of hydrogen sulfide (H2S) on aging-related cardiovascular risk factors and mechanisms. The results showed that D-gal treatment increased the levels of p16, p53, p21 proteins, and senescence-associated beta-galactosidase staining. The greater sympathetic responses in aged rats were associated with increased inflammation, as well as decreased levels of klotho in the paraventricular nucleus. However, the administration of H2S reduced sympathetic activity and improved cellular senescence, inflammation, and klotho levels.
The present study aimed to explore the central relationship between cardiovascular conditions and aging. D-galactose (D-gal) was utilized to induce an accelerated aging model and to evaluate the effects of hydrogen sulfide (H2S) on aging-related cardiovascular risk factors and mechanisms. Eight-week-old Sprague Dawley rats were given an intraperitoneal injection of 250 mg/kg D-gal every day with or without H2S (56 mu mol/kg) for 12 weeks. We found that D-gal treatment induced a noticeably aging-related increase in p16, p53 and p21 protein levels and senescence-associated beta-galactosidase staining. In addition, the level of noradrenalin was increased, accompanied by enhanced blood pressure and renal sympathetic nerve activity in aged rats. The greater sympathetic responses were related with the increased level of inflammation. The decreased level of klotho in the paraventricular nucleus neuron also contributed to sympathetic activation in D-gal-induced aged rats. However, the exogenous administration of H2S attenuated the sympathetic activity in aged rats, as evidenced by the decreased blood pressure, renal sympathetic nerve activity and noradrenalin level. The ameliorated cellular senescence, inflammation and heightened klotho in the paraventricular nucleus were attributed to the protective effects of H2S. The present study provides further evidence for the drug development of H2S for the prevention or treatment of the aging-associated cardiovascular diseases.

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