4.7 Article

Protection by -Biotics against Hypertension Programmed by Maternal High Fructose Diet: Rectification of Dysregulated Expression of Short-Chain Fatty Acid Receptors in the Hypothalamic Paraventricular Nucleus of Adult Offspring

期刊

NUTRIENTS
卷 14, 期 20, 页码 -

出版社

MDPI
DOI: 10.3390/nu14204306

关键词

programmed hypertension; maternal high fructose diet; microbial metabolites; short-chain fatty acids; prebiotics; probiotics; synbiotics; butyrate; G-protein coupled receptor 41; olfactory receptor 78; hypothalamic paraventricular nucleus

资金

  1. Chang Gung Medical Foundation, Taiwan [CMRPG8J0261-0263, CLRPG8J0031-0032]
  2. Ministry of Science and Technology, Taiwan [MOST109-2320-B-182A-006, MOST110-2320-B-182A-020, MOST111-2320-B-182A-015]

向作者/读者索取更多资源

This study explored the role of short-chain fatty acids (SCFAs) and SCFA-sensing receptors in the developmental programming of hypertension in offspring exposed to a high fructose diet (HFD) during maternal gestation and lactation. The study found that dysregulated levels of SCFAs and expression of SCFA-sensing receptors in the hypothalamic paraventricular nucleus (PVN) were associated with increased oxidative stress and neuroinflammation in the PVN of HFD offspring. Additionally, supplementation with prebiotics, probiotics, synbiotics, and postbiotics improved these dysfunctions and protected against programmed hypertension in adult HFD offspring.
The role of short-chain fatty acids (SCFAs) in the brain on the developmental programming of hypertension is poorly understood. The present study explored dysregulated tissue levels of SCFAs and expression of SCFA-sensing receptors in the hypothalamic paraventricular nucleus (PVN), a key forebrain region engaged in neural regulation of blood pressure of offspring to maternal high fructose diet (HFD) exposure. We further investigated the engagement of SCFA-sensing receptors in PVN in the beneficial effects of -biotics (prebiotic, probiotic, synbiotic, and postbiotic) on programmed hypertension. Maternal HFD during gestation and lactation significantly reduced circulating butyrate, along with decreased tissue level of butyrate and increased expression of SCFA-sensing receptors, GPR41 and olfr78, and tissue oxidative stress and neuroinflammation in PVN of HFD offspring that were rectified by oral supplement with -biotics. Gene silencing of GPR41 or olfr78 mRNA in PVN also protected adult HFD offspring from programmed hypertension and alleviated the induced oxidative stress and inflammation in PVN. In addition, oral supplement with postbiotic butyrate restored tissue butyrate levels, rectified expressions of GPR41 and olfr78 in PVN, and protected against programmed hypertension in adult HFD offspring. These data suggest that alterations in tissue butyrate level, expression of GPR41 and olfr78, and activation of SCFA-sensing receptor-dependent tissue oxidative stress and neuroinflammation in PVN could be novel mechanisms that underlie hypertension programmed by maternal HFD exposure in adult offspring. Furthermore, oral -biotics supplementation may exert beneficial effects on hypertension of developmental origin by targeting dysfunctional SCFA-sensing receptors in PVN to exert antioxidant and anti-inflammatory actions in the brain.

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