Orexin A attenuates palmitic acid-induced hypothalamic cell death

Cayla M. Duffy, Joshua P Nixon, Tammy A. Butterick

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21 Scopus citations


Palmitic acid (PA), an abundant dietary saturated fatty acid, contributes to obesity and hypothalamic dysregulation in part through increase in oxidative stress, insulin resistance, and neuroinflammation. Increased production of reactive oxygen species (ROS) as a result of PA exposure contributes to the onset of neuronal apoptosis. Additionally, high fat diets lead to changes in hypothalamic gene expression profiles including suppression of the anti-apoptotic protein B cell lymphoma 2 (Bcl-2) and upregulation of the pro-apoptotic protein B cell lymphoma 2 associated X protein (Bax). Orexin A (OXA), a hypothalamic peptide important in obesity resistance, also contributes to neuroprotection. Prior studies have demonstrated that OXA attenuates oxidative stress induced cell death. We hypothesized that OXA would be neuroprotective against PA induced cell death. To test this, we treated an immortalized hypothalamic cell line (designated mHypoA-1/2) with OXA and PA. We demonstrate that OXA attenuates PA-induced hypothalamic cell death via reduced caspase-3/7 apoptosis, stabilization of Bcl-2 gene expression, and reduced Bax/Bcl-2 gene expression ratio. We also found that OXA inhibits ROS production after PA exposure. Finally, we show that PA exposure in mHypoA-1/2 cells significantly reduces basal respiration, maximum respiration, ATP production, and reserve capacity. However, OXA treatment reverses PA-induced changes in intracellular metabolism, increasing basal respiration, maximum respiration, ATP production, and reserve capacity. Collectively, these results support that OXA protects against PA-induced hypothalamic dysregulation, and may represent one mechanism through which OXA can ameliorate effects of obesogenic diet on brain health.

Original languageEnglish (US)
Pages (from-to)93-100
Number of pages8
JournalMolecular and Cellular Neuroscience
StatePublished - Sep 1 2016

Bibliographical note

Funding Information:
This work was funded by the U.S. Department of Veterans Affairs BLR&D IK2 BX001686 and IS1 BX003083A (to TAB), the University of Minnesota Healthy Foods, Healthy Lives Institute (to JPN and TAB), and the Minnesota Veterans Medical Research & Education Foundation (to TAB), and the Minnesota Obesity Center (NIH/NIDDK NORC Grant P30 DK050456). We also thank Dr. David A Bernlohr and Dr. Rocio Foncea for their assistance with the Seahorse assays.

Publisher Copyright:
© 2016


  • Apoptosis
  • Hypocretin
  • Neurodegeneration
  • Neuroprotection
  • Palmitic acid
  • Reactive oxygen species


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