Journal
NEUROMOLECULAR MEDICINE
Volume 24, Issue 4, Pages 363-373Publisher
HUMANA PRESS INC
DOI: 10.1007/s12017-022-08706-1
Keywords
COVID-19; ACE2; Circumventricular organs; Subfornical organ; Area postrema; Pineal gland; OVLT; Paraventricular nucleus of the hypothalamus
Categories
Funding
- Ministry of Education [NUHSRO/2019/051/T1/Seed-Mar/04]
- National Medical Research Council of Singapore [HLCA21Jan-0019]
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SARS-CoV-2 can enter cells by binding to ACE2, and it may enter the brain through circumventricular organs and the hypothalamus. Binding of the virus with ACE2 could lead to a reduction in the ACE2 / Ang (1-7) / Mas receptor signaling pathway, affecting neural activity and the hypothalamic-pituitary-adrenal axis. The virus may also affect the hypothalamus via transneuronal spread along olfactory/limbic pathways. Exploring potential therapeutic pathways to prevent or reduce neurological symptoms of COVID-19 is important.
The SARS-CoV-2 virus gains entry to cells by binding to angiotensin-converting enzyme 2 (ACE2). Since circumventricular organs and parts of the hypothalamus lack a blood-brain barrier, and immunohistochemical studies demonstrate that ACE2 is highly expressed in circumventricular organs which are intimately connected to the hypothalamus, and the hypothalamus itself, these might be easy entry points for SARS-CoV-2 into the brain via the circulation. High ACE2 protein expression is found in the subfornical organ, area postrema, and the paraventricular nucleus of the hypothalamus (PVH). The subfornical organ and PVH are parts of a circuit to regulate osmolarity in the blood, through the secretion of anti-diuretic hormone into the posterior pituitary. The PVH is also the stress response centre in the brain. It controls not only pre-ganglionic sympathetic neurons, but is also a source of corticotropin-releasing hormone, that induces the secretion of adrenocorticotropic hormone from the anterior pituitary. It is proposed that the function of ACE2 in the circumventricular organs and the PVH could be diminished by binding with SARS-CoV-2, thus leading to a reduction in the ACE2/Ang (1-7)/Mas receptor (MasR) signalling axis, that modulates ACE/Ang II/AT1R signalling. This could result in increased presympathetic activity/neuroendocrine secretion from the PVH, and effects on the hypothalamic-pituitary-adrenal axis activity. Besides the bloodstream, the hypothalamus might also be affected by SARS-CoV-2 via transneuronal spread along the olfactory/limbic pathways. Exploring potential therapeutic pathways to prevent or attenuate neurological symptoms of COVID-19, including drugs which modulate ACE signalling, remains an important area of unmet medical need.
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