Sidney Rafilson, Nathan Gonzales Hess, Teresa M Findley, Matthew C Smear
{"title":"从嗅球局部场电位推断呼吸节奏的挑战。","authors":"Sidney Rafilson, Nathan Gonzales Hess, Teresa M Findley, Matthew C Smear","doi":"10.1093/chemse/bjaf026","DOIUrl":null,"url":null,"abstract":"<p><p>Odors convey useful navigational and episodic information, yet much of the chemical world remains inaccessible without active sampling through sniffing. Respiratory cycles control odor dynamics within the nose, so understanding olfactory bulb (OB) neural dynamics requires accurate respiratory measurements. While respiratory behavior can be measured directly with a variety of chronic methods, these methods are invasive, and none are perfectly robust. OB local field potentials (LFPs) have long been known to couple with respiration. Here, we investigated whether the precise timing and frequency of respiration can be inferred from OB LFPs. Our results replicate previous findings that OB LFPs across multiple frequency bands align with respiratory cycles. Further, these OB rhythms are locked to time in the respiratory cycle, and not phase. In addition, we show that 2 to 12 Hz LFP oscillations effectively track sniffing rate. However, a monotonic relationship between LFP-respiratory delay and sniffing rate, which varies across animals, renders the recovery of precise respiratory events challenging. This work underscores the complex and individualized relationship between rodent respiration and OB LFPs, contributing to our understanding of how respiration controls olfaction.</p>","PeriodicalId":9771,"journal":{"name":"Chemical Senses","volume":" ","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12402772/pdf/","citationCount":"0","resultStr":"{\"title\":\"Challenges in inferring breathing rhythms from olfactory bulb local field potentials.\",\"authors\":\"Sidney Rafilson, Nathan Gonzales Hess, Teresa M Findley, Matthew C Smear\",\"doi\":\"10.1093/chemse/bjaf026\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Odors convey useful navigational and episodic information, yet much of the chemical world remains inaccessible without active sampling through sniffing. Respiratory cycles control odor dynamics within the nose, so understanding olfactory bulb (OB) neural dynamics requires accurate respiratory measurements. While respiratory behavior can be measured directly with a variety of chronic methods, these methods are invasive, and none are perfectly robust. OB local field potentials (LFPs) have long been known to couple with respiration. Here, we investigated whether the precise timing and frequency of respiration can be inferred from OB LFPs. Our results replicate previous findings that OB LFPs across multiple frequency bands align with respiratory cycles. Further, these OB rhythms are locked to time in the respiratory cycle, and not phase. In addition, we show that 2 to 12 Hz LFP oscillations effectively track sniffing rate. However, a monotonic relationship between LFP-respiratory delay and sniffing rate, which varies across animals, renders the recovery of precise respiratory events challenging. This work underscores the complex and individualized relationship between rodent respiration and OB LFPs, contributing to our understanding of how respiration controls olfaction.</p>\",\"PeriodicalId\":9771,\"journal\":{\"name\":\"Chemical Senses\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-01-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12402772/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Senses\",\"FirstCategoryId\":\"102\",\"ListUrlMain\":\"https://doi.org/10.1093/chemse/bjaf026\",\"RegionNum\":4,\"RegionCategory\":\"心理学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BEHAVIORAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Senses","FirstCategoryId":"102","ListUrlMain":"https://doi.org/10.1093/chemse/bjaf026","RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
Challenges in inferring breathing rhythms from olfactory bulb local field potentials.
Odors convey useful navigational and episodic information, yet much of the chemical world remains inaccessible without active sampling through sniffing. Respiratory cycles control odor dynamics within the nose, so understanding olfactory bulb (OB) neural dynamics requires accurate respiratory measurements. While respiratory behavior can be measured directly with a variety of chronic methods, these methods are invasive, and none are perfectly robust. OB local field potentials (LFPs) have long been known to couple with respiration. Here, we investigated whether the precise timing and frequency of respiration can be inferred from OB LFPs. Our results replicate previous findings that OB LFPs across multiple frequency bands align with respiratory cycles. Further, these OB rhythms are locked to time in the respiratory cycle, and not phase. In addition, we show that 2 to 12 Hz LFP oscillations effectively track sniffing rate. However, a monotonic relationship between LFP-respiratory delay and sniffing rate, which varies across animals, renders the recovery of precise respiratory events challenging. This work underscores the complex and individualized relationship between rodent respiration and OB LFPs, contributing to our understanding of how respiration controls olfaction.
期刊介绍:
Chemical Senses publishes original research and review papers on all aspects of chemoreception in both humans and animals. An important part of the journal''s coverage is devoted to techniques and the development and application of new methods for investigating chemoreception and chemosensory structures.