Language：English   Publishing type：Research paper (scientific journal)   Publisher：Springer Science and Business Media LLC  

We have previously shown that pituitary adenylate cyclase-activating polypeptide (PACAP) in the ventromedial hypothalamus (VMH) enhances feeding during the dark cycle and after fasting, and inhibits feeding during the light cycle. On the other hand, galanin is highly expressed in the hypothalamus and has been reported to be involved in feeding regulation. In this study, we investigated the involvement of the VMH-PACAP to the dorsomedial hypothalamus (DMH)-galanin signaling in the regulation of feeding. Galanin expression in the hypothalamus was significantly increased with fasting, but this increment was canceled in PACAP-knockout (KO) mice. Furthermore, overexpression of PACAP in the VMH increased the expression of galanin, while knockdown (KD) of PACAP in the VMH decreased the expression of galanin, indicating that the expression of galanin in the hypothalamus might be regulated by PACAP in the VMH. Therefore, we expressed the synaptophysin-EGFP fusion protein (SypEGFP) in PACAP neurons in the VMH and visualized the neural projection to the hypothalamic region where galanin was highly expressed. A strong synaptophysin-EGFP signal was observed in the DMH, indicating that PACAP-expressing cells of the VMH projected to the DMH. Furthermore, galanin immunostaining in the DMH showed that galanin expression was weak in PACAP-KO mice. When galanin in the DMH was knocked down, food intake during the dark cycle and after fasting was decreased, and food intake during the light cycle was increased, as in PACAP-KO mice. These results indicated that galanin in the DMH may regulate the feeding downstream of PACAP in the VMH.

DOI： 10.1007/s12035-022-03084-y

Scopus

PubMed

Other Link： https://link.springer.com/article/10.1007/s12035-022-03084-y/fulltext.html

Language：Japanese   Publishing type：Research paper (scientific journal)  

Brain glycogen metabolism is known to be involved in the learning and memory processes. Protein targeting to glycogen (PTG) is a crucial molecule for glycogenesis, and its expression level is shown to be increased in the dorsal hippocampus during fear memory acquisition and recall, suggesting that PTG may contribute to the memory process. However, its detailed role in the dorsal hippocampus remains unclear. Therefore, we knocked down the expression of PTG in the dorsal hippocampus and attempted to analyze its function behaviorally. PTG expression was found to be enriched in astrocytes. Furthermore, short hairpin RNA against PTG suppressed the expression of PTG in astrocytes. Mice with knockdown of PTG in the dorsal hippocampus showed suppressed alternation behavior in the Y-maze test and reduced memory recall at the first hour after acquisition in the passive avoidance test. Knockdown of mouse dorsal hippocampal astrocyte-specific PTG also impaired working memory in the Y-maze test. GluR1, GluR2, and NR2a subunits expressions were significantly down-regulated in the dorsal hippocampus of mice in which PTG was knocked down. These results indicate that PTG in the dorsal hippocampal astrocytes may contribute to working and short-term memories by maintaining the expression of glutamate receptor subunits.

DOI： 10.1016/j.jphs.2021.10.008

Scopus

PubMed

Language：English   Publisher：(公社)日本薬理学会  

マウスの背側海馬におけるprotein targeting to glycogen(PTG)の発現をノックダウンし、PTGの機能を行動学的に解析した。PTGはアストロサイトで高発現していた。PTGに対するshRNAはアストロサイトにおけるPTG発現を抑制した。背側海馬のPTGをノックダウンしたマウスではY迷路試験での交替行動、および受動回避試験での記憶の獲得から1時間後にて想起が抑制された。マウス背側海馬のアストロサイト特異的PTGのノックダウンにより、Y迷路試験での作業記憶に障害が生じた。PTGノックダウンマウスの背側海馬で、GluR1、GluR2およびNR2aサブユニットの発現が下方制御された。

Language：Japanese   Publisher：The Japanese Dental Society of Anesthesiology  

<p>  In patients with single ventricle heart disease, non-cardiac surgery using the Glenn procedure can be performed to alleviate cyanosis prior to repair using the Fontan procedure. We performed general anesthesia management during lip repair and palatoplasty in a patient with left ventricular hypoplasia following a Glenn procedure.</p><p>  The patient underwent lip repair at an age of 1 year and 2 months and a palatoplasty at the age of 1 year and 10 months. During the preoperative examinations, hemorrhagic diathesis, hypoxemia, and secondary polycythemia were observed.</p><p>  General anesthesia was induced using midazolam, fentanyl, and remifentanil and was maintained using fentanyl and sevoflurane in oxygen (F<span style="font-variant: small-caps;">io</span>₂=0.47). Low blood pressure was treated with the administration of an α1 receptor stimulant or volume expansion with infusion to prevent an increase in pulmonary vascular resistance and to maintain the pulmonary blood flow. In addition, pulmonary blood flow was maintained by increased oxygen administration and mild hyperventilation, inhibiting any deterioration in oxygenation through the maintenance of blood flow. After the palatoplasty, hypoxemia and intraoral bleeding were observed, and reintubation was performed.</p><p>  Patients who are scheduled to undergo a palatoplasty have a high risk of bleeding because the wound surface remains in front of the palate. In addition, the risk of bleeding increases in patients with cyanosis because of the use of antithrombotic drugs, the increase in collateral blood flow, and the presence of secondary polycythemia.</p><p>  In conclusion, the risks of increased pulmonary vascular resistance, hypoxemia, and increased bleeding must be considered for safe anesthesia during a palatoplasty in patients with cyanotic heart disease.</p>

DOI： 10.24569/jjdsa.47.2_65

Scopus

Event date： 2022.10

Language：Japanese  

Event date： 2022.3

Language：Japanese   Presentation type：Oral presentation (general)  

Venue：Fukuoka   Country：Japan  

DOI： https://doi.org/10.1254/jpssuppl.95.0_1-SS-14

Event date： 2021.3

Language：Japanese   Presentation type：Symposium, workshop panel (nominated)  

Event date： 2020.11

Language：Japanese  

Event date： 2020.10

Event date： 2019.11

Event date： 2019.10

Language：Japanese  

Event date： 2019.8

Event date： 2019.6

Language：Japanese