Cardiogenic control of affective behavioural state.
Brian HsuehRitchie ChenYoungJu JoDaniel TangMisha RaffieeYoon Seok KimMasatoshi InoueSawyer RandlesCharu RamakrishnanSneha PatelDoo Kyung KimTony X LiuSoo Hyun KimLongzhi TanLeili MortazaviArjay CorderoJenny ShiMingming ZhaoTheodore T HoAiley CrowAi-Chi Wang YooCephra RajaKathryn EvansDaniel BernsteinMichael ZeinehMaged GoubranKarl DeisserothPublished in: Nature (2023)
Emotional states influence bodily physiology, as exemplified in the top-down process by which anxiety causes faster beating of the heart 1-3 . However, whether an increased heart rate might itself induce anxiety or fear responses is unclear 3-8 . Physiological theories of emotion, proposed over a century ago, have considered that in general, there could be an important and even dominant flow of information from the body to the brain 9 . Here, to formally test this idea, we developed a noninvasive optogenetic pacemaker for precise, cell-type-specific control of cardiac rhythms of up to 900 beats per minute in freely moving mice, enabled by a wearable micro-LED harness and the systemic viral delivery of a potent pump-like channelrhodopsin. We found that optically evoked tachycardia potently enhanced anxiety-like behaviour, but crucially only in risky contexts, indicating that both central (brain) and peripheral (body) processes may be involved in the development of emotional states. To identify potential mechanisms, we used whole-brain activity screening and electrophysiology to find brain regions that were activated by imposed cardiac rhythms. We identified the posterior insular cortex as a potential mediator of bottom-up cardiac interoceptive processing, and found that optogenetic inhibition of this brain region attenuated the anxiety-like behaviour that was induced by optical cardiac pacing. Together, these findings reveal that cells of both the body and the brain must be considered together to understand the origins of emotional or affective states. More broadly, our results define a generalizable approach for noninvasive, temporally precise functional investigations of joint organism-wide interactions among targeted cells during behaviour.
Keyphrases
- heart rate
- resting state
- white matter
- functional connectivity
- induced apoptosis
- left ventricular
- cerebral ischemia
- blood pressure
- cell cycle arrest
- healthcare
- type diabetes
- sars cov
- heart failure
- bipolar disorder
- multiple sclerosis
- cell death
- adipose tissue
- drug delivery
- metabolic syndrome
- endoplasmic reticulum stress
- blood brain barrier
- genome wide
- signaling pathway
- mass spectrometry
- cell proliferation
- wild type
- high speed
- prefrontal cortex
- inferior vena cava