TY - JOUR
T1 - Diameter of fluorescent microspheres determines their distribution throughout the cortical watershed area in mice
AU - Tsukada, Naoki
AU - Katsumata, Masahiro
AU - Oki, Koichi
AU - Minami, Kazushi
AU - Abe, Takato
AU - Takahashi, Shinichi
AU - Itoh, Yoshiaki
AU - Suzuki, Norihiro
N1 - Funding Information:
This work was supported by a Grant-in-Aid for Scientific Research (C) from the Ministry of Education , Culture, Sports, Science, and Technology of Japan : 24591276 (Shinichi Takahashi) and 15 K09324 (Shinichi Takahashi).
Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2018/1/15
Y1 - 2018/1/15
N2 - A hemodynamic mechanism has long been assumed to play an important role in watershed infarction. In recent years, however, clinical evidence has indicated that an embolic mechanism is involved. The mechanism by which emboli are trapped preferentially in watershed areas remains unclear. In the present study, we developed a mouse embolus model using fluorescent microspheres with different diameters and evaluated the role of the microspheres’ diameters in the generation of a watershed-patterned distribution. We injected fluorescent microspheres of four different diameters (i.e., 13, 24, 40, and 69 μm) into the internal carotid artery of C57BL/6 mice either (1) without ligation of the common carotid artery (normal perfusion pressure model: NPPM) or (2) with ligation of the common carotid artery (low perfusion pressure model: LPPM). Left common carotid artery ligation induced reductions in local cerebral blood flow in both the periphery and the core area of the left middle cerebral artery. A greater reduction in the border-zone area between the left anterior cerebral artery and the middle cerebral artery was also noted. After 24 h, the brains were removed and the distribution of the microspheres in the brain was evaluated using a fluorescence microscope. The 24-μm microspheres were distributed in the watershed area more frequently than the other microsphere sizes (P <.05, ANOVA followed by Tukey's test). Meanwhile, the distribution rates were similar between the NPPM and LPPM models for all microsphere sizes. This study suggested that the distribution pattern of the microspheres was only affected by the microspheres’ diameters.
AB - A hemodynamic mechanism has long been assumed to play an important role in watershed infarction. In recent years, however, clinical evidence has indicated that an embolic mechanism is involved. The mechanism by which emboli are trapped preferentially in watershed areas remains unclear. In the present study, we developed a mouse embolus model using fluorescent microspheres with different diameters and evaluated the role of the microspheres’ diameters in the generation of a watershed-patterned distribution. We injected fluorescent microspheres of four different diameters (i.e., 13, 24, 40, and 69 μm) into the internal carotid artery of C57BL/6 mice either (1) without ligation of the common carotid artery (normal perfusion pressure model: NPPM) or (2) with ligation of the common carotid artery (low perfusion pressure model: LPPM). Left common carotid artery ligation induced reductions in local cerebral blood flow in both the periphery and the core area of the left middle cerebral artery. A greater reduction in the border-zone area between the left anterior cerebral artery and the middle cerebral artery was also noted. After 24 h, the brains were removed and the distribution of the microspheres in the brain was evaluated using a fluorescence microscope. The 24-μm microspheres were distributed in the watershed area more frequently than the other microsphere sizes (P <.05, ANOVA followed by Tukey's test). Meanwhile, the distribution rates were similar between the NPPM and LPPM models for all microsphere sizes. This study suggested that the distribution pattern of the microspheres was only affected by the microspheres’ diameters.
KW - Carotid stenosis
KW - Embolic infarction
KW - Fluorescent microsphere
KW - Hemodynamic infarction
KW - Watershed infarction
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U2 - 10.1016/j.brainres.2017.11.028
DO - 10.1016/j.brainres.2017.11.028
M3 - Article
C2 - 29203170
AN - SCOPUS:85037336311
SN - 0006-8993
VL - 1679
SP - 109
EP - 115
JO - Molecular Brain Research
JF - Molecular Brain Research
ER -