2020.12.24 (木)
小腸分野を研究していて、
・細胞で結果が出たのだけれど、動物実験では異なった
・吸収モデル実験を小腸単体で行いたい
・小腸への薬物Doseコントロールを直接行いたい
・上腸間膜静脈から直接サンプリングしたい
といったことはありませんか?
ラットから小腸を摘出し、臓器培養システムにて20時間の灌流培養後も、蠕動運動を認め、灌流率を維持した。
動物個体では解析することのできない、小腸単体での解析を可能にするため、活性を保ち、解析可能な状態での灌流培養を目指した。 灌流率は、下の式で定義した。
灌流率=静脈からの戻り量(g)/送液量(g)
20時間の灌流培養し、蠕動運動を認め、40%前後の灌流率を維持しながら灌流することができた(Fig.1)。
灌流後の組織切片では、平滑筋、粘膜様組織を維持していたことが示唆された(Fig.2)。
これにより、活性を保ち、且つ静脈からの戻り液を解析可能な状態での灌流培養を実現した。
Sano, K. et al. J Artif Organs (2019)
Have you ever felt following needs during the studying of the small intestine?
“The results came differently when you are working with cells and animals. Do not know why.”
“I want to perform absorption model experiments in the small intestine alone.”
“I want to control drug dosage to the small intestine directly.”
“I want to sample directly from the superior mesenteric vein.”
The small intestine chamber of our “Organ Culture System” allows you to run small intestinal perfusion experiments in rats surprisingly easily.
In this issue, I would like to introduce an example of the experiment.
For graphs and tissue slices images can be downloaded here.
The small intestine was removed from the rat and after 20 hours of perfusion culture in the Organ Culture System, it showed peristalsis and maintained its perfusion rate.
To allow analysis in the isolated small intestine, which is not possible to analyze in individual animals, we aimed to achieve a perfusion culture that remained active and ready for analysis.
The perfusion rate was defined by the following equation.
Perfusion rate = return volume from vein (g)/infused volume (g)
20 hours of perfusion culture, peristalsis was observed, and perfusion while maintaining a perfusion rate of around 40%. It was possible (Fig. 1).
In the perfused tissue sections, smooth muscle and mucosal-like tissue were maintained (Fig. 2).
These results suggest that the tissue section after perfusion maintained its activity and the return fluid from the vein could be analyzed (Fig.2).
Sano, K. et al. J Artif Organs (2019) link
Realizing ex-vivo isolated perfusion culture of organs.
Proven results in rat skeletal muscle and rat small intestine.
Other organs are also available for customization as much as possible.
Have you ever felt following needs during the studying of the small intestine?
“The results came differently when you are working with cells and animals. Do not know why.”
“I want to perform absorption model experiments in the small intestine alone.”
“I want to control drug dosage to the small intestine directly.”
“I want to sample directly from the superior mesenteric vein.”
The small intestine chamber of our “Organ Culture System” allows you to run small intestinal perfusion experiments in rats surprisingly easily.
In this issue, I would like to introduce an example of the experiment.
For graphs and tissue slices images can be downloaded here.
The small intestine was removed from the rat and after 20 hours of perfusion culture in the Organ Culture System, it showed peristalsis and maintained its perfusion rate.
To allow analysis in the isolated small intestine, which is not possible to analyze in individual animals, we aimed to achieve a perfusion culture that remained active and ready for analysis.
The perfusion rate was defined by the following equation.
Perfusion rate = return volume from vein (g)/infused volume (g)
20 hours of perfusion culture, peristalsis was observed, and perfusion while maintaining a perfusion rate of around 40%. It was possible (Fig. 1).
In the perfused tissue sections, smooth muscle and mucosal-like tissue were maintained (Fig. 2).
These results suggest that the tissue section after perfusion maintained its activity and the return fluid from the vein could be analyzed (Fig.2).
Sano, K. et al. J Artif Organs (2019) link