Role of microglia in blood pressure and respiratory responses to acute hypoxic exposure in rats

• Published in: The journal of physiological sciences Vol. 72; no. 1; p. 26
• Main Authors: Yoshizawa, Masashi, Fukushi, Isato, Takeda, Kotaro, Kono, Yosuke, Hasebe, Yohei, Koizumi, Keiichi, Ikeda, Keiko, Pokorski, Mieczyslaw, Toda, Takako, Okada, Yasumasa
• Format: Journal Article
• Language: English
• Published: Japan Springer 13.10.2022; BioMed Central
• Subjects: Abdomen; Animals; Blood Pressure; Coronary vessels; Digitization; Heart rate; Hypoxia; Hypoxia - metabolism; Laboratory animals; Lung - metabolism; Microglia; Microglia - metabolism; Minocycline; Minocycline - metabolism; Minocycline - pharmacology; Original Paper; Physiology; Rats; Recovery (Medical); Variance analysis; Ventilation; Ventilatory behavior; Japan; Cardiorespiratory regulation; Blood pressure telemetry; Hypoxic ventilatory response; Acute hypoxia; Microglia
• ISSN: 1880-6546; 1880-6562
• DOI: 10.1186/s12576-022-00848-y

Microglia modulate cardiorespiratory activities during chronic hypoxia. It has not been clarified whether microglia are involved in the cardiorespiratory responses to acute hypoxia. Here we investigated this issue by comparing cardiorespiratory responses to two levels of acute hypoxia (13% O for 4 min and 7% O for 5 min) in conscious unrestrained rats before and after systemic injection of minocycline (MINO), an inhibitor of microglia activation. MINO increased blood pressure but not lung ventilation in the control normoxic condition. Acute hypoxia stimulated cardiorespiratory responses in MINO-untreated rats. MINO failed to significantly affect the magnitude of hypoxia-induced blood pressure elevation. In contrast, MINO tended to suppress the ventilatory responses to hypoxia. We conclude that microglia differentially affect cardiorespiratory regulation depending on the level of blood oxygenation. Microglia suppressively contribute to blood pressure regulation in normoxia but help maintain ventilatory augmentation in hypoxia, which underscores the dichotomy of central regulatory pathways for both systems.