Photomodulatory effects in the hypothalamus of sleep-deprived young and aged rats

Behav Brain Res. 2024 Feb 26:458:114731. doi: 10.1016/j.bbr.2023.114731. Epub 2023 Oct 26.

Abstract

Insufficient sleep is associated with impaired hypothalamic activity and declined attentional performance. In this study, alterations in the hypothalamus of REM sleep-deprived (SD) young and aged rats, and the modulatory effect of near-infrared (NIR) laser were investigated. Forty-eight male Wistar rats (24 young at 2 months and 24 senile at 14 months) were divided into three groups: the control, the SD group subjected to 72 hr of sleep deprivation, and the transcranial-NIR laser-treated (TLT) group subjected to SD for 72 hr and irradiated with 830 nm laser. The hypothalamic levels of oxidative stress, inflammatory biomarkers, antioxidant enzymes, mitochondrial cytochrome C oxidase (CCO), apoptotic markers (BAX, BCL-2), and neuronal survival-associated genes (BDNF, GLP-1) were evaluated. Furthermore, the hypothalamic tissue alterations were analyzed via histological examination. The results revealed that TLT treatment has enhanced the antioxidant status, prevented oxidative insults, suppressed neuroinflammation, regulated CCO activity, reduced apoptotic markers, and tuned the survival genes (BDNF & GLP-1) in hypothalamic tissue of SD young and aged rats. Microscopically, TLT treatment has ameliorated the SD-induced alterations and restored the normal histological features of hypothalamus tissue. Moreover, the obtained data showed that SD and NIR laser therapy are age-dependent. Altogether, our findings emphasize the age-dependent adverse effects of SD on the hypothalamus and suggest the use of low-laser NIR radiation as a potential non-invasive and therapeutic approach against SD-induced adverse effects in young and aged animals.

Keywords: Aging; Cytochrome C oxidase; Hypothalamus; Photobiomodulation; REM sleep-deprivation.

MeSH terms

  • Animals
  • Antioxidants* / pharmacology
  • Brain-Derived Neurotrophic Factor* / metabolism
  • Glucagon-Like Peptide 1
  • Hypothalamus / metabolism
  • Male
  • Rats
  • Rats, Wistar
  • Sleep Deprivation / complications

Substances

  • Antioxidants
  • Brain-Derived Neurotrophic Factor
  • Glucagon-Like Peptide 1