Substance P Reduces Infarct Size and Mortality After Ischemic Stroke, Possibly Through the M2 Polarization of Microglia/Macrophages and Neuroprotection in the Ischemic Rat Brain

• Published in: Cellular and molecular neurobiology Vol. 43; no. 5; pp. 2035 - 2052
• Main Authors: Ahn, Woosung, Chi, Guangfan, Kim, Sumin, Son, Youngsook, Zhang, Mingzi
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.07.2023; Springer Nature B.V
• Subjects: Amino acids; Biomedical and Life Sciences; Biomedicine; Blood-brain barrier; Bone marrow; Brain injury; CD11b antigen; CD163 antigen; Cell Biology; Cerebral blood flow; Endothelial cells; Inflammation; Ischemia; Macrophages; Mesenchymal stem cells; Microenvironments; Microglia; Monocytes; Mortality; Neurobiology; Neuroprotection; Neurosciences; Original Research; Pericytes; Polarization; Recovery of function; Reperfusion; Stroke; Substance P; M2 monocyte/macrophages; Neuroprotection; Stroke; Ischemia; Substance-P; Blood–brain barrier
• ISSN: 0272-4340; 1573-6830
• DOI: 10.1007/s10571-022-01284-7

Substance-P (SP) is an 11 amino acid neuropeptide that is known to stimulate the peripheral mobilization of bone marrow mesenchymal stem cells and M2 polarization in monocytes/macrophages in a variety of acute and chronic tissue injuries. To examine the role of SP in protection and recovery from acute ischemic brain injury, experimental ischemic stroke was induced by transient middle cerebral artery occlusion (tMCAo) in rats for 1 h with subsequent reperfusion. Two injections of SP, immediately and one day post-tMCAo, resulted in approximately threefold lower mortality and 40% less infarct volume than those of saline-treated rats at seven days post-tMCAo. At 4.5 h, SP markedly increased CD11b/c + CD163 + /CD 206 + cells in the blood, which were concomitantly decreased in the bone marrow, suggesting that SP preferentially mobilized M2-polarized monocytes. After two days, SP increased the expression of neuroprotective and anti-inflammatory genes in the ischemic brain and induced neuronal survival in the brain penumbra. Additionally, SP markedly increased CD68 + CD163 + and CD68 + CD206 + M2 microglia/macrophages in the ischemic brain during seven days post-tMCAo. Furthermore, SP preserved the blood‒brain barrier in the ischemic brain, which was confirmed by the abundant levels of SMI71 + brain endothelial cells that colocalized with α-SMA + pericytes. The beneficial effects of SP on functional recovery and tissue preservation were maintained for six weeks. Collectively, SP treatment in the early phase of ischemic stroke markedly suppressed the destructive inflammatory response and improved the microenvironment for tissue protection and repair.