Repeated activation of C1 neurons in medulla oblongata decreases anti-inflammatory effect via the hypofunction of the adrenal gland adrenergic response

• Published in: Brain, behavior, and immunity behavior, and immunity, 2023-07, Vol.111, p.138-150
• Main Authors: Abe, Chikara, Katayama, Chikako, Bazek, Murat, Nakamura, Yasuna, Ohbayashi, Kento, Horii, Kazuhiro, Fujimoto, Chisato, Tanida, Mamoru, Iwasaki, Yusaku, Inoue, Tsuyoshi, Nin, Fumiaki, Morita, Hironobu
• Format: Article
• Language: English
• Subjects: Adrenal Glands; Adrenergic Agents - pharmacology; Anti-inflammatory; Anti-Inflammatory Agents - pharmacology; Autonomic nervous system; Chemogenetic; Medulla Oblongata - physiology; Neurons; Norepinephrine - pharmacology; Optogenetic
• ISSN: 0889-1591; 1090-2139
• DOI: 10.1016/j.bbi.2023.04.003

•Short-term activation of C1 neurons exerts a protection against acute lung injury.•Both splenic sympathetic nerve and adrenal gland are important for the protection against acute lung injury.•Repeated long-term activation of C1 neurons eliminated the protective effect against acute lung injury.•Repeated activation of C1 neurons deteriorates adrenal gland adrenergic response. The immune system is known to be controlled by the autonomic nervous system including sympathetic and parasympathetic (vagus) nerves. C1 neurons in the medulla oblongata, which participate in the control of the autonomic nervous system, are responders to stressors and regulate the immune system. Short-term activation of C1 neurons suppresses inflammation, while the effect of a long-term activation of these neurons on the inflammatory reflex is unclear. We, herein, demonstrate that the coactivation of both the splenic sympathetic nerves and the adrenal gland adrenergic response are indispensable for the prognosis of acute lung injury. The chemogenetic activation of C1 neurons increased plasma catecholamine including adrenaline and noradrenaline levels. The deletion of catecholaminergic cells using local injections of viral vector in the adrenal gland abolished the protective effect against acute lung injury when the C1 neurons were stimulated by either chemogenetic or optogenetic tools. Furthermore, repeated activation of C1 neurons using chemogenetic tool inhibited the adrenal response without affecting the plasma noradrenaline levels, eliminated the protective effect against acute lung injury. This was rescued by the isoprenaline administration. We concluded that the maintenance of an adrenergic response via C1 neurons in the adrenal gland is a prerequisite for the delivery of an effective anti-inflammatory response.