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  3. Hungry for Knowledge: Octopamine Signaling Regulates Hunger-Enhanced Olfactory Learning

Hungry for Knowledge: Octopamine Signaling Regulates Hunger-Enhanced Olfactory Learning

  • Adv Sci (Weinh). 2025 Dec 15:e13842. doi: 10.1002/advs.202513842.
Huijuan Zhao 1 2 3,  Guiyuan Shi 1 2 3,  Ruixue Qin 1 2 3,  Yinghao Sun 1 2 3,  Wenbo Guo 4,  Ruixia Shi 1,  Minxian Peng 5,  Jingxuan Yang 6,  Jianjian Zhao 7,  Qiuhan Liu 1,  Jun Xiao 8,  Ke Zhang 1 2 3,  Qiang Liu 5,  Wenxing Yang 6,  He Liu 1 2 3
Affiliations

Affiliations

  • 1 Department of Systems Science, Faculty of Arts and Sciences, Beijing Normal University, Zhuhai, Guangdong, 519000, China.
  • 2 International Academic Center of Complex Systems, Beijing Normal University, Zhuhai, Guangdong, 519000, China.
  • 3 School of Systems Science, Beijing Normal University, Beijing, 100062, China.
  • 4 MOE Key Lab of Bioinformatics, BNRIST Bioinformatics Division, Department of Automation, Tsinghua University, Beijing, 100084, China.
  • 5 Department of Neuroscience, City University of Hong Kong, Tat Chee Avenue, Kowloon Tong, Hong Kong, 610200, China.
  • 6 Department of Physiology, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, Sichuan, 610041, China.
  • 7 Guangdong Institute of Intelligence Science and Technology, Zhuhai, Guangdong, 510050, China.
  • 8 Laboratory Safety and Equipment Management Office, Beijing Normal University, Zhuhai, Guangdong, 519000, China.
PMID: 41392936 DOI: 10.1002/advs.202513842
Abstract

Hunger, a state of nutrient deficiency, significantly enhances cognitive behaviors by heightening sensitivity to food-related stimuli. However, the mechanisms by which hunger influences olfactory learning remain unclear. In this study, it is shown that aversive or appetitive memory is formed faster in hungry C. elegans. These findings reveal that hunger-induced octopamine release from the interneuron RIC enhances both aversive and appetitive olfactory learning. By analyzing neural circuits downstream of RIC, two distinct pathways involved in memory formation are identified. For aversive learning, the sensory neuron ASH is activated via the SER-3 receptor, leading to glutamate release, which acts on the GLR-2 receptor in AIA interneuron during the starvation phase. During the training section, AIA is subsequently inhibited via the glutamate-gated Chloride Channel GLC-3. In contrast, octopamine targets AIY interneurons through the SER-6 receptor, promoting appetitive learning. Furthermore, it is indicated that norepinephrine, the mammalian homolog of octopamine, and alpha1-adrenergic receptors may be involved in hunger-enhanced olfactory learning in mice. These findings may offer insights into the neural mechanisms that underlie cognitive flexibility in response to physiological states.

Keywords

C. elegans; hunger; neural circuits; norepinephrine; octopamine; olfactory learning.

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