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초록
AI-Helper 아이콘AI-Helper

목적 : 본 논문에서는 경락을 추적하기 위한 피내(皮內) 알시안 블루(Alcian blue) 염색 방법을 기술한다. 방법 : 1% 알시안 블루 용액을 31게이지 바늘이 달린 0.5mL 인슐린 주사기를 사용하여 경혈 지점에 피내 주사한 후 실체 현미경하에서 수술, 관찰하였다. 면역조직화학적 방법을 사용하여 해당 조직을 레이저 공초점주사현미경으로 관찰하였다. 결과 : 알시안 블루로 염색되고 피하로 이어지는 실 모양 구조물을 관찰하였다. 이 조직 내에서 특징적인 막대모양 핵 배열 및 $1-2{\mu}m$크기의 데옥시리보핵산 입자가 관찰되었다. 또한 경혈 조직 내에서 풍부한 모세혈관총 및 말초신경 말단, 그리고 약 $300{\mu}m$크기의 소체형 구조물을 확인하였다. 결론 : 경혈 지점의 피내에서 발견된 특징적 실 모양 구조물 및 소체형 구조물은 각각 표층 봉한관 및 소체로 판단된다.

Abstract AI-Helper 아이콘AI-Helper

Objective In this article, we report on the intradermal Alcian blue staining method for tracing the meridians of acupuncture. Methods 1% Alcian blue solution was injected into acupoints by using a 0.5mL insulin syringe with a 31-gauge needle, then the skin was incised and was observed under a stereo...

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AI 본문요약
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제안 방법

  • The samples were fixed in 4% paraformaldehyde (PFA) solution for 1 hour, washed with phosphate buffered solution(PBS), and then stained with DAPI solution(SlowFade Gold, Invitrogen, Oregon, USA) for 10minutes in a dark place. After staining, the samples were covered by a coverslip and examined under a phase contrast microscope (BX51, Olympus, Japan) at the excitation wavelength of 350nm for detection of DAPI fluorescence(emission wavelength: 470nm) from cell nuclei.
  • 5g/kg) administered intraperitoneally. All experimental procedures including surgery were performed under deep anesthesia. The animals were kept in the sternal recumbency position.
  • To stain blood vessels, sections were incubated with mouse monoclonal RECA-1 antibody(diluted 1:50, 1 day, Abcam, UK ). Visualization was performed by using Alexa Flour 488-conjugated goat anti-mouse IgG(H+L)(diluted 1:500, 1 day, Invitrogen, USA). All incubations of thick sections with primary and secondary antibodies were carried out at 4℃.

대상 데이터

  • Male Wistar rats of 10 -12weeks old were used in this study. The animals were housed in a temperature-controlled environment(23℃) with 60% relative humidity with a 12-h light/dark cycle.
  • Two hours after injection, the dorsal skin was incised, from the LSP region to the scapula region, with operation knives and scissors. The stained parts of the skin were observed under a stereoscopic microscope(SZX 12, Olympus, Japan), and images were taken by a digital camera(Nikon, Japan) and a CCD camera(DP 70, Olympus, Japan). After observation, the Ab-stained regions were sampled for histologial analyses.
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참고문헌 (25)

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