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. 2020 Mar 3;11:75. doi: 10.3389/fneur.2020.00075

Table 1.

Effects of apelin/APJ signaling on ischemic stroke.

Experimental model Pathway Effect References
Mice in vivo (MCAO) ↑PI3K/AKT, ↑ERK Protection (46, 47)
Rats in vivo (MCAO) ↑ERK Protection (48)
Mice in vivo (MCAO) ↑AMPK Protection (49)
Rats in vivo (MCAO)/OGD/R cell model neurons ↑Gαi/Gαq-CK2,
↓eIF2-ATF4-CHOP
Protection (14)
Rats in vivo (MCAO) ↓ERS/UPR Protection (13)
Mice in vivo (MCAO)/neonatal H/I injury rat model ↑PI3K/AKT Protection (50)
Mice in vivo (MCAO) ↓JNK, ↓P38MAPK Protection (45)
Rats in vivo (MCAO)/OGD/R cell model neurons ↑VEGF–VEGFR2,
↑ERK, ↑PI3K/AKT
Protection (51)
Rats in vivo (MCAO)/PC12 cells ↑AMPK/GSK-3β/Nrf2 Protection (52)

MCAO, middle cerebral artery occlusion; P13K, phosphatidylinositide 3-kinase; ERK, extracellular signal-regulated kinase; AMPK, AMP-activated protein kinase; CK2, casein kinase 2; OGD/R, oxygen-glucose deprivation/reperfusion; ATF4, activating transcription factor 4; CHOP, CCAAT/enhancer binding protein homologous protein; ERS, endoplasmic reticulum stress; UPR, unfolded protein response; H/I, hypoxia/ischemia; JNK, C-Jun N-terminal kinase; P38MAPK, p38 mitogen-activated protein kinase; VEGF, vascular endothelial growth factor; VEGFR, VEGF receptor; GSK-3β, glycogen synthase kinase 3 β; Nrf2, nuclear factor erythroid 2–related factor 2.