• 제목/요약/키워드: aquaporin 1 (AQP1)

검색결과 58건 처리시간 0.025초

신유(腎兪),태계(太谿)의 동충하초(冬蟲夏草) 약침(藥鍼)과 경구(經口) 투여(投與)가 좌측 신장(腎臟) 제거 백서(白鼠)에 대한 신장(腎臟) Aquaporin-2 단백(蛋白) 발현(發現)과 신장기능(腎臟機能)에 미치는 영향(影響) (Effects of Cordyceps Militaris Mycelia(CMM) oral administration and Herbal Acupuncture at Shinsu(BL23), Tae-gye(K3) on Expression of Aquaporin-2 Protein Water Channels in the Kidney and the Renal Function in Rats with Renal Failure by Uninephrectomy)

  • 김재홍;윤대환;나창수;조명래;윤여충;채우석
    • Journal of Acupuncture Research
    • /
    • 제22권1호
    • /
    • pp.61-75
    • /
    • 2005
  • 동충하초(冬蟲夏草)가 신장(腎臟)기능에 미치는 영향을 실험적으로 규명하고자 부분 신절제술을 시행한 백서(白鼠)에 대하여 동충하초(冬蟲夏草) 경구투여(經口投與)와 신유(腎兪) 태계(太谿)에 약침(藥鍼)을 시행한 후 신장내(腎臟內) aquaporin -2 단백발현과 혈장내 renin, ANP, aldosterone 등의 혈액 학적 변화 및 뇨중 creatinine, Na, K Cl 를 관찰하여 다음과 같은 결과를 얻었다. 1. AQP2단백 발현은 경구투여(經口投與) 1, 3군, 약침(藥鍼) 1군에서 유의한 증가를 나타내었다. 2. 혈장 renin은 경구투여(經口投與) 1, 2, 3군, 약침(藥鍼) 1, 2, 3 군 모두에서 유의한 감소를 나타내었다. 3. 혈장 ANP는 경구투여(經口投與) 1군, 약침(藥鍼 ) 3군에서 유의한 증가를 나타내었다. 4. 혈장 aldosterone은 경구투여(經口投與) 2, 3군, 약침(藥鍼) 2군에서 유의한 감소를 나타내었다. 5. 혈청 triglyceride는 경구투여(經口投與) 2, 3군, 약침(藥鍼) 2, 3군에서 유의한 감소를 나타내었다. 6. 혈청 albumin은 경구투여(經口投與) 2군, 약침(藥鍼) 3군에서 유의한 증가를 나타내었다. 7. 혈청 total protein, BUN은 경구투여(經口投與) 1, 2, 3 군, 약침(藥鍼) 1, 2, 3군 모두에서 유의한 감소를 나타내었다. 8. 혈청 phosphorus는 경구투여(經口投與) 1, 2, 3군, 약침(藥鍼) 1, 2군에서 유의한 감소를 나타내었다. 9. 뇨(尿) creatinine은 경구투여(經口投與) 2군에서 유의한 증가를 나타내었고, 약침(藥鍼)군에서는 유의한 변화가 관찰되지 않았다. 10. 뇨(尿) Na는 경구투여(經口投與 ) 1, 2군, 약침(藥鍼) 1, 2, 3군에서 유의한 증가를 나타내었다. 11. 뇨 K는 경구투여(經口投與) 1, 3군에서 유의한 감소를 나타내었으나, 약침(藥鍼) 3군에서는 유의한 증가를 나타내었다. 12. 뇨 Cl는 경구투여(經口投與) 3군, 약침(藥鍼) 2, 3군에서 유의한 증가를 나타내었다.

  • PDF

The Anti-Wrinkle Mechanism of Ganoderma lucidum mycelial with Acorus gramineus callus in UVB Treated HaCaT Keratinocytes

  • Eun-Sil Ko;Sang-Min Cho;Sol Lee;Ji-Hye Jung;Jea-Ran Kang;Jong-Hoon Jeong;Dong-gue Shin;Jeong Hun Seo;Jeong-Dan Cha
    • 한국자원식물학회:학술대회논문집
    • /
    • 한국자원식물학회 2020년도 춘계학술대회
    • /
    • pp.74-74
    • /
    • 2020
  • Skin is continuously exposed to a variety of environmental stresses, including ultraviolet (UV) radiation. UVB is an inherent component of sunlight that crosses the epidermis and reaches the upper dermis, leading to increased oxidative stress, activation of inflammatory response and accumulation of DNA damage among other effects. In the present study, the anti-wrinkle mechanism of Acorus gramineus callus culture supernatant (GB-AGS-PSC) was elucidated in UVB treated HaCaT keratinocytes. GB-AGS-PSC prevented the matrix metalloprotease 1 (MMP-1), elastin, and pro-collagen product and cytotoxicity and SOD inhibition. Quantitative polymerase chain reaction showed that GB-AGS-PSC-treated cells displayed dose-dependent increase in messenger RNA expression levels of Aquaporin 3 (AQP3), Keratin 1(KRT1), fillagrin, and hyaluronan synthase-2 (HAS 2) and decreased expression levels of matrix metalloproteinase-3, -9, and -13 in UVB treated HaCaT keratinocytes. Additionally, GB-AGS-PSC suppressed TNF-α, IL-1β, and IL-8 product for inflammatory responses in UVB treated HaCaT keratinocytes. Therefore, GB-AGS-PSC may be useful as an anti-photoaging resource for the skin.

  • PDF

이너뷰티 소재로서의 생물전환된 가시오가피-진피 혼합 추출물의 생물학적 활성 (Biological Activity of Mixed Extracts of Acanthopanax senticosus and Citrus unshiu Fermented with Bovista plumbea for Inner Beauty)

  • 김은정;김소연;강수연;유영춘;윤택준;이계원;조영호
    • 생명과학회지
    • /
    • 제33권7호
    • /
    • pp.555-564
    • /
    • 2023
  • 본 연구에서는 이너뷰티용 소재로서의 활용가능성을 확인하기 위하여 생물전환 가시오가피-진피 혼합추출물(B-MEAC)의 항산화 활성, 엘라스타제 억제활성 및 피부보습 효과 등을 평가하였다. B-MEAC의 항산화 활성을 측정한 결과 DPPH radical을 농도의존적으로 소거하여 SC50이 156.1±0.82 ㎍/ml로 나타났다. 또한, 엘라스타제 억제활성을 측정한 결과 B-MEAC 처리 농도 의존적으로 엘라스타제 활성을 억제하는 것으로 확인되었다(p<0.001). 경구투여한 B-MEAC가 마우스 피부 보습에 미치는 영향을 확인하기 위하여 피부 수분량과 경피수분손실량을 측정한 결과 건조유도 된 대조군에 비하여 피부 수분량은 증가하고(p<0.001), 경피수분손실량은 감소하는 것으로 나타났다(p<0.01). 또한, 건조유도 된 마우스 피부의 교원섬유 변화에 미치는 영향을 Masson's trichrome 염색을 통해 관찰한 결과 B-MEAC를 투여한 군에서 콜라겐의 양이 대조군에 비해 상대적으로 증가하여 푸른색으로 보다 진하게 염색되었다. 또한, 건조유도 된 마우스 피부의 보습 기능에 미치는 영향을 확인하기 위하여 보습 관련 인자들의 발현을 Western blot 기법으로 확인한 결과 B-MEAC를 투여한 군에서 대조군에 비하여 MMP-1 단백질의 발현량은 감소하였고, COL1A1, HAS2, filaggrin, AQP3 단백질 발현량은 회복되는 것으로 나타났다(p<0.001). 따라서 B-MEAC의 보습효과는 엘라스타제 활성 억제, MMP-1 발현 감소, 콜라겐 생성 촉진, 피부 보습 관련 단백질인 HAS2 및 AQP3 발현 증가, 피부 장벽기능의 중요인자인 filaggrin 발현 증가를 통한 수분량 증가와 TEWL 감소에 의해 나타나는 것으로 이너뷰티 소재로서의 개발 가능성을 제시한다.

염분 변화에 따른 무지개송어(Oncorhynchus mykiss)의 삼투조절 유전자 발현변화 (Gene Expression Profiles of Rainbow Trout Oncorhynchus mykiss after Salinity Challenge)

  • 최영광;박흠기;김이경
    • 한국수산과학회지
    • /
    • 제54권5호
    • /
    • pp.676-684
    • /
    • 2021
  • Euryhaline teleost have extraordinary ability to deal with a wide range of salinity changes. To study the seawater adaptability of rainbow trout Oncorhynchus mykiss (body weight 638±54 g, length 38.6±2 cm) to salinity increase fish were transferred from freshwater to 7, 14, 21, 28 and 32 psu and checked for mortality over 5 days. No mortality was observed in 0-32 psu. In fish transferred to 0-32 psu, blood osmolality was maintained within physiological range. The changes of serum enzyme activities (aspartate transaminase, AST and alanine transaminase, ALT) showed no significant level during experimental period. To explore the underlying molecular physiology of gill and kidney responsible for body fluid regulation, we measured mRNA expression of five genes, Na+/K+/2Cl- cotransporter1 (NKCC1), aquaporin3 (AQP3), cystic fibrosis transmembrane conductance regulator (CFTR), glucocorticoid receptor (GR) and growth hormone receptor (GHR) in response to salt stress. Based on our result, rainbow trout could tolerate gradual transfer up to 32 psu for 5 days without mortality under physiological stress. This study suggests to alleviate osmotic stress to fish, a gradually acclimation to increasing salinity is recommended.

The Effect of γ-Aminobutyric Acid Intake on UVB- Induced Skin Damage in Hairless Mice

  • Hairu Zhao;Bomi Park;Min-Jung Kim;Seok-Hyun Hwang;Tae-Jong Kim;Seung-Un Kim;Iksun Kwon;Jae Sung Hwang
    • Biomolecules & Therapeutics
    • /
    • 제31권6호
    • /
    • pp.640-647
    • /
    • 2023
  • The skin, the largest organ in the body, undergoes age-related changes influenced by both intrinsic and extrinsic factors. The primary external factor is photoaging which causes hyperpigmentation, uneven skin surface, deep wrinkles, and markedly enlarged capillaries. In the human dermis, it decreases fibroblast function, resulting in a lack of collagen structure and also decreases keratinocyte function, which compromises the strength of the protective barrier. In this study, we found that treatment with γ-aminobutyric acid (GABA) had no toxicity to skin fibroblasts and GABA enhanced their migration ability, which can accelerate skin wound healing. UVB radiation was found to significantly induce the production of matrix metalloproteinase 1 (MMP-1), but treatment with GABA resulted in the inhibition of MMP-1 production. We also investigated the enhancement of filaggrin and aquaporin 3 in keratinocytes after treatment with GABA, showing that GABA can effectively improve skin moisturization. In vivo experiments showed that oral administration of GABA significantly improved skin wrinkles and epidermal thickness. After the intake of GABA, there was a significant decrease observed in the increase of skin thickness measured by calipers and erythema. Additionally, the decrease in skin moisture and elasticity in hairless mice exposed to UVB radiation was also significantly restored. Overall, this study demonstrates the potential of GABA as functional food material for improving skin aging and moisturizing.

레몬그라스와 자소엽 추출물의 피부보습 및 피부장벽에 관한 연구 (Skin Hydration and Skin Barrier Effects of Cymbopogon citratus and Perilla frutescens Extracts)

  • 소양강;황지영;김현우;조하늘;이태범
    • 대한화장품학회지
    • /
    • 제45권3호
    • /
    • pp.225-235
    • /
    • 2019
  • 레몬그라스와 자소엽 추출물은 다양한 생리 효과를 나타내는 것으로 알려져 있지만, 피부보습과 피부장벽에 미치는 영향은 아직까지 연구되지 않았다. 본 연구에서는 레몬그라스와 자소엽 추출물의 피부보습과 피부장벽에 미치는 영향과 페놀성 화합물을 분석하였다. 피부각질형성세포에서 각 추출물이 피부보습에 미치는 영향을 조사한 결과, 두 추출물 모두 물보다 에탄올 추출물에서 히알루론산 생성이 많았다. HPLC를 이용한 19종 페놀성 화합물 분석 결과는 레몬그라스 에탄올 추출물(CCE)에서 chlorogenic acid와 p-coumaric acid가 검출되었으며 자소엽 에탄올 추출물(PFE)에서 rosmarinic acid와 caffeic acid가 검출되었다. 피부보습에 관련된 HAS1, HAS2, HAS3 및 AQP3와 피부장벽에 관련된 filaggrin, loricrin 발현은 PFE보다 CCE에서 높았다. 또한, CCE, PFE 모두 피부보습과 표피분화 조절에 관여하는 $PPAR-{\alpha}$ 단백질의 발현이 농도 의존적으로 증가하였으며 CCE의 주요성분인 chlorogenic acid와 p-coumaric acid가 $PPAR-{\alpha}$ 발현을 증가시켰다. 결론적으로 피부보습과 피부장벽보호 효과에 있어서 CCE가 PFE보다 우수한 효과를 나타내었고, 두 추출물은 피부보습과 피부장벽개선에 대한 기능성 소재로써 활용될 수 있을 것이라 생각된다.

Epigallocatechin-3-Gallate (EGCG) Attenuates Traumatic Brain Injury by Inhibition of Edema Formation and Oxidative Stress

  • Zhang, Bo;Wang, Bing;Cao, Shuhua;Wang, Yongqiang
    • The Korean Journal of Physiology and Pharmacology
    • /
    • 제19권6호
    • /
    • pp.491-497
    • /
    • 2015
  • Traumatic brain injury (TBI) is a major cause of mortality and long-term disability, which can decrease quality of life. In spite of numerous studies suggesting that Epigallocatechin-3- gallate (EGCG) has been used as a therapeutic agent for a broad range of disorders, the effect of EGCG on TBI remains unknown. In this study, a weight drop model was established to evaluate the therapeutic potential of EGCG on TBI. Rats were administered with 100 mg/kg EGCG or PBS intraperitoneally. At different times following trauma, rats were sacrificed for analysis. It was found that EGCG (100 mg/kg, i.p.) treatment significantly reduced brain water content and vascular permeability at 12, 24, 48, 72 hour after TBI. Real-time PCR results revealed that EGCG inhibited TBI-induced IL-$1{\beta}$ and TNF-${\alpha}$ mRNA expression. Importantly, CD68 mRNA expression decreasing in the brain suggested that EGCG inhibited microglia activation. Western blotting and immunohistochemistry results showed that administering of EGCG significantly inhibited the levels of aquaporin-4 (AQP4) and glial fibrillary acidic protein (GFAP) expression. TBI-induced oxidative stress was remarkably impaired by EGCG treatment, which elevated the activities of SOD and GSH-PX. Conversely, EGCG significantly reduced the contents of MDA after TBI. In addition, EGCG decreased TBI-induced NADPH oxidase activation through inhibition of $p47^{phox}$ translocation from cytoplasm to plasma membrane. These data demonstrate that EGCG treatment may be an effective therapeutic strategy for TBI and the underlying mechanism involves inhibition of oxidative stress.

Evaluation of Potential Biomarkers for Thioacetamide-induced Hepatotoxicity using siRNA

  • Kang, Jin-Seok;Yum, Young-Na;Han, Eui-Sik;Kim, Joo-Hwan;Lee, Eun-Mi;Ryu, Doug-Young;Kim, Young-Hee;Yang, Sung-Hee;Kim, Seung-Hee;Park, Sue-Nie
    • Biomolecules & Therapeutics
    • /
    • 제16권3호
    • /
    • pp.197-202
    • /
    • 2008
  • In our previous publication we compared the gene expression profiles on hepatotoxicants exposure to assess the comparability between in vivo and in vitro test systems. We investigated global gene expression from both mouse liver and mouse hepatic cell line treated with thioacetamide (TAA) and identified several common genes. In this study, we selected genes to validate them as potential biomarkers for hepatotoxicity on the relevance of in vitro and in vivo system. Three up-regulated, aquaporin 8 (Aqp8), glutathione peroxidase 1 (Gpx1), succinate-CoA ligase, GDP-forming, alpha subunit (Suclg1) and two down-regulated, DnaJ (Hsp40) homolog subfamily C member 5 (Dnajc5) and tumor protein D52 (Tpd52) genes were tested for their effects in vitro. For characterization of gene function, short interfering RNA (siRNA) for each gene was synthesized and transfected in mouse hepatic cell line, BNL CL.2. Cell viability, mRNA expression level and morphological alterations were investigated. We confirmed siRNA transfection against selected five genes induced down-regulation of respective mRNA expression. siRNA transfection in general decreased cell viability in different degrees and induced morphological changes such as membrane thickening and alterations of intracellular structures. This suggests that these genes could be associated with TAA-induced toxicity. Furthermore, these genes may be used in the investigation of hepatotoxicity for better understanding of its mechanism.