Beneficial effects of the phytoestrogen genistein on hippocampal impairments of spontaneously hypertensive rats (SHR)

• Published in: Journal of neuroendocrinology 2023-01, Vol.35 (1), p.e13228-n/a
• Main Authors: Ronchetti, Santiago, Labombarda, Florencia, Roig, Paulina, De Nicola, Alejandro F., Pietranera, Luciana
• Format: Article
• Language: English
• Subjects: 17β-Estradiol; Animals; Astrocytes; Cognitive ability; Cyclooxygenase 2 - metabolism; Dentate gyrus; Doublecortin Domain Proteins; Doublecortin protein; Encephalopathy; Estrogen receptors; Estrogens; Genistein; Genistein - pharmacology; Glial fibrillary acidic protein; Glial Fibrillary Acidic Protein - metabolism; Glial stem cells; Growth factors; Hippocampus; Hippocampus - metabolism; Hypertension; Immunocytochemistry; Inflammation; Membrane proteins; Microglia; mRNA; Neural stem cells; neuroinflammation; Neuronal-glial interactions; Neuroprotection; Pattern recognition; Phenotypes; Phytoestrogens - metabolism; Phytoestrogens - pharmacology; Prostaglandin endoperoxide synthase; Proteins; Rats; Rats, Inbred SHR; Rats, Inbred WKY; Receptors, Estradiol - metabolism; RNA, Messenger - metabolism; Transforming Growth Factor beta - metabolism; Transforming growth factor-b; Tumor Necrosis Factor-alpha - metabolism; Tumor necrosis factor-TNF; Tumor necrosis factor-α
• ISSN: 0953-8194; 1365-2826
• DOI: 10.1111/jne.13228

Hippocampal neuropathology is a recognized feature of the spontaneously hypertensive rat (SHR). The hippocampal alterations associate with cognitive impairment. We have shown that hippocampal abnormalities are reversed by 17β‐estradiol, a steroid binding to intracellular receptors (estrogen receptor α and β subtypes) or the membrane‐located G‐protein coupled estradiol receptor. Genistein (GEN) is a neuroprotective phytoestrogen which binds to estrogen receptor β and G‐protein coupled estradiol receptor. Here, we investigated whether GEN neuroprotection extends to SHR. For this purpose, we treated 5‐month‐old SHR for 2 weeks with 10 mg kg−1 daily s.c injections of GEN. We analyzed the expression of doublecortin+ neuronal progenitors, glial fibrillary acidic protein+ astrocytes and ionized calcium‐binding adapter molecule 1+ microglia in the CA1 region and dentate gyrus of the hippocampus using immunocytochemistry, whereas a quantitative real‐time polymerase chain reaction was used to measure the expression of pro‐ and anti‐inflammatory factors tumor necrosis factor α, cyclooxygenase‐2 and transforming growth factor β. We also evaluated hippocampal dependent memory using the novel object recognition test. The results showed a decreased number of doublecortin+ neural progenitors in the dentate gyrus of SHR that was reversed with GEN. The number of glial fibrillary acidic protein+ astrocytes in the dentate gyrus and CA1 was increased in SHR but significantly decreased by GEN treatment. Additionally, GEN shifted microglial morphology from the predominantly activated phenotype present in SHR, to the more surveillance phenotype found in normotensive rats. Furthermore, treatment with GEN decreased the mRNA of the pro‐inflammatory factors tumor necrosis factor α and cyclooxygenase‐2 and increased the mRNA of the anti‐inflammatory factor transforming growth factor β. Discrimination index in the novel object recognition test was decreased in SHR and treatment with GEN increased this parameter. Our results indicate important neuroprotective effects of GEN at the neurochemical and behavioral level in SHR. Our data open an interesting possibility for proposing this phytoestrogen as an alternative therapy in hypertensive encephalopathy. GEN treatment produced neuroprotective effects in the hippocampus of the SHR animals similar to those produced by 17β‐estradiol: it increased neurogenesis in DG, attenuate dastrogliosis and reverted the microglial phenotype towards a prof