4.7 Article

Cerebral A1 adenosine receptor availability in female and male participants and its relationship to sleep

期刊

NEUROIMAGE
卷 245, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2021.118695

关键词

Adenosine receptors; A1AR; PET; Sex differences; [18F]CPFPX; Sleep

资金

  1. Institute for Scientific Information of Coffee (ISIC)
  2. Swiss National Science Foundation [320030_163439]
  3. Clinical Research Priority Program Sleep & Health of the University of Zurich
  4. DLR Management Board Young Research Group Leader Program
  5. project SleepLess - BMBF [01EW1808]
  6. FWO
  7. FRQS
  8. Aeronautics Program of the German Aerospace Centre
  9. Swiss National Science Foundation (SNF) [320030_163439] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

Our study found that A(1) adenosine receptor availability is higher in healthy females compared to males even under well-rested conditions, particularly in regions such as the pallidum and anterior cingulate cortex. This difference in receptor availability may partially explain the known sex differences in sleep efficiency and latency, suggesting a potential role of adenosine in sleep-wake control.
The neuromodulator adenosine and its receptors are mediators of sleep-wake regulation which is known to differ between sexes. We, therefore, investigated sex differences in A(1) adenosine receptor (A(1)AR) availability in healthy human subjects under well-rested conditions using [F-18]CPFPX and positron emission tomography (PET). [F-18]CPFPX PET scans were acquired in 50 healthy human participants (20 females; mean age +/- SD 28.0 +/- 5.3 years). Mean binding potential (BPND ; Logan's reference tissue model with cerebellum as reference region) and volume of distribution (V-T) values were calculated in 12 and 15 grey matter brain regions, respectively. [F-18]CPFPX BPND was higher in females compared to males in all investigated brain regions (p < 0.025). The largest differences were found in the pallidum and anterior cingulate cortex, where mean BPND values were higher by 29% in females than in males. In females, sleep efficiency correlated positively and sleep latency negatively with BP ND in most brain regions. V-T values did not differ between sexes. Sleep efficiency correlated positively with V-T in most brain regions in female participants. In conclusion, our analysis gives a first indication for potential sex differences in A(1)AR availability even under well-rested conditions. A(1)AR availability as measured by [F-18]CPFPX BPND is higher in females compared to males. Considering the involvement of adenosine in sleep-wake control, this finding might partially explain the known sex differences in sleep efficiency and sleep latency.

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