The Role of Piromelatine on Peripheral and Hippocampal Insulin Resistance in Rat Offspring Exposed to Chronic Maternal Stress

• Published in: International journal of molecular sciences 2024-06, Vol.25 (13), p.7022
• Main Authors: Ivanova, Natasha, Atanasova, Milena, Terzieva, Dora, Georgieva, Katerina, Tchekalarova, Jana
• Format: Article
• Language: English
• Subjects: Animals; Blood Glucose - metabolism; Cognition & reasoning; Diabetes; Female; Females; Glucose; Glucose Transporter Type 4 - metabolism; Hippocampus - drug effects; Hippocampus - metabolism; HOMA-IR; Homeostasis; Hyperglycemia; insulin; Insulin - blood; Insulin - metabolism; insulin receptor; Insulin Resistance; Male; Melatonin; Melatonin - pharmacology; melatonin analog; Memory; Metabolism; Plasma; Pregnancy; Prenatal Exposure Delayed Effects - metabolism; prenatal stress; Rats; Rats, Sprague-Dawley; Receptor, Insulin - metabolism; Stress, Psychological - metabolism
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25137022

Prenatal stress (PNS), which alters the hypothalamic-pituitary-adrenal axis function in the offspring, predisposes to insulin resistance (IR) in later life and is associated with numerous disorders, including cognitive and memory impairments. At present, our main goal is to assess the effects of chronic piromelatine (Pir) administration, a melatonin analogue, on PNS-provoked IR in the periphery and the hippocampus in male and female offspring. Pregnant Sprague-Dawley rats were exposed to chronic stress (one short-term stressor on a daily basis and one long-term stressor on a nightly basis) from the first gestation week until birth. Vehicle or Pir 20 mg/kg were administered intraperitoneally for 21 days. Plasma glucose, serum insulin levels, and the homeostasis model assessment of insulin resistance (HOMA-IR) were determined as markers of peripheral IR. For the hippocampal IR assessment, insulin receptors (IRs) and glucose transporter 4 (GLUT4) were examined. Prenatally stressed offspring of both sexes indicated enhanced plasma glucose and serum insulin concentrations, increased HOMA-IR, and decreased hippocampal GLUT4 only in male rats. The PNS-induced changes were corrected by chronic treatment with Pir. The present results suggest that the melatoninergic compound Pir exerts beneficial effects on altered glucose/insulin homeostasis in PNS-exposed offspring.