Hydrogen sulfide in the paraventricular nucleus attenuates endoplasmic reticulum stress in Spontaneous hypertension.
Hydrogen sulfide (H2S), known as a metabolic modulator, is a gaseous signaling molecule with functions similar to those of nitric oxide and carbon monoxide, all of which possess vasodilatory, antioxidant, and other properties. In the central nervous system, H2S is a signaling molecule that is crucial for neuroprotection and the control of neurological processes. The paraventricular nucleus (PVN) of the hypothalamus is an important central nucleus that regulates and integrates cardiovascular and peripheral sympathetic activity. This study aimed to investigate whether intra-PVN injection of the endogenous H2S synthase CBS activator S-adenosylmethionine (SAMe) or the endogenous H2S synthase CBS inhibitor hydroxylamine (HA) modulates H2S expression in the PVN, whether microglia in the PVN are targeted by H2S, and whether PVN H2S further induces alterations in blood pressure(BP) by affecting endoplasmic reticulum(ER) stress in the PVN of spontaneously hypertensive rats (SHR). Healthy male Wistar-Kyoto (WKY) rats and SHR were fed a normal diet for 8weeks, followed by intra-PVN injections of SAMe, HA, or vehicle for 4weeks. Plasma norepinephrine levels and mean arterial pressure were elevated in the SHR group. The expression of factors related to ER stress, such as p-PERK, GRP78, and p-IRE1α, was also elevated. Levels of these parameters were lower in the SHR+SAMe group, whereas the SHR + HA group presented with higher levels of these indicators. These findings suggest that endogenous H2S attenuates sympathetic activity and hypertensive responses in the PVN, in part by modulating ER stress.
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