• 제목/요약/키워드: Collagen production

검색결과 457건 처리시간 0.032초

폐경 여성의 골 건강과 L-ascorbic acid (Bone Health and L-ascorbic acid in Postmenopausal Women)

  • 김보경;김미향
    • 생명과학회지
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    • 제31권12호
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    • pp.1142-1148
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    • 2021
  • 인간의 평균수명이 연장되면서 폐경 이후 여성의 삶의 질에도 많은 관심을 가지게 되었다. 한국인 여성에서 폐경이 나타나는 시기는 평균적으로 49.7세로 알려져 있으며, 폐경 이후의 삶이 일생의 1/3 이상을 차지하게 되어 주요한 사회적 문제로 대두되고 있다. L-ascorbic acid (AsA)는 생물의 에너지 대사과정에서 필수적인 조효소로 작용하고 있으며, 특히, 골 구성 단백질인 collagen의 합성 및 성숙에 관여하고 있는 것으로 알려져 있다. 따라서 본 연구에서는 폐경 여성에서의 AsA와 골 건강에 대해 소개하고자 하였다. AsA는 collagen 생합성에 중요한 인자이며, collagen은 골을 구성하는 단백질로써 골 기질의 석회화를 위해 필요한 물질이므로 골 건강에 대한 AsA의 역할은 대단히 중요하다는 것을 알 수 있다. Collagen 가교는 동물의 성장 과정에서 collagen 섬유의 안정화 및 탄력성을 위해 필요한 것이나, 과잉의 증가는 세포 간 영양소 또는 노폐물의 이동이 억제되어 더욱 노화로 연결되기 쉽다. AsA는 collagen 미숙가교 형성에 환원제로 작용하여 미숙가교를 안정화하여, 미숙가교에서 성숙가교인 pyridinoline이 생성되는 반응을 억제시킨다. 따라서, AsA는 collagen 생합성에 관여하여 골 조직의 건강에 도움을 주는 한편, collagen 가교의 지나친 성숙을 조절하여 폐경 여성에게서 나타날 수 있는 골 관련 문제에 중요한 역할을 할 것으로 추측된다. 이상의 정보는 폐경 여성의 골 건강에 대한 향후 연구에 기초자료로 이용될 수 있을 것으로 기대된다.

Spinach Saponin-Enriched Fraction Inhibits Platelet Aggregation in cAMP- and cGMP-Dependent Manner by Decreasing TXA2 Production and Blood Coagulation

  • Cho, Hyun-Jeong;Choi, Sun-A;Kim, Chun-Gyu;Jung, Tae-Sung;Hong, Jeong-Hwa;Rhee, Man-Hee;Park, Hye-Jin;Park, Hwa-Jin
    • Biomolecules & Therapeutics
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    • 제19권2호
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    • pp.218-223
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    • 2011
  • In this study, we investigated the effect of spinach saponin-enriched fraction (SSEF) on collagen (10 ${\mu}g/ml$)-stimulated platelet aggregation. SSEF inhibited collagen-induced platelet aggregation, and which was involved in the inhibition of thromboxane $A_2$ ($TXA_2$) production, an intracellular $Ca^{2+}$-agonist as an aggregation-inducing autacoidal molecule. In addition, SSEF significantly increased the formation of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), intracellular $Ca^{2+}$-antagonists as aggregation-inhibiting molecules, in collagen-stimulated platelets. These results suggest that SSEF might inhibit $Ca^{2+}$-elevation and $TXA_2$ formation by increasing the production of $Ca^{2+}$-antagonistic molecules cAMP and cGMP. These mean that SSEF is a potent inhibitor of collagen-stimulated platelet aggregation. On the other hand, prothrombin time (PT) and activated partial thromboplastin time (APTT) were potently prolonged by SSEF. These findings suggest that SSEF prolongs the internal time between the conversion of fibrinogen to fibrin. Accordingly, our data demonstrate that SSEF may be a crucial tool for a negative regulator during platelet activation and blood coagulation on thrombotic diseases.

Effects of Avocado Yoghurt, Three Beans Cookie, and Tiger Nut Galsu Drink on Fibroblasts (Hs68) and Keratinocytes (HaCaT)

  • Park, Seung-Yong;Jung, Eun-Kyung;Joo, Nami;Shin, Hyun-Soo;Shin, Ji-Sun;Myoung, Da-Bin;Lee, Kyung-Tae
    • Journal of Dairy Science and Biotechnology
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    • 제37권2호
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    • pp.136-153
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    • 2019
  • The present study aimed to investigate the effects of skin care foods on the synthesis of pro-collagen type I C peptide and suppression of matrix metalloproteinase (MMP)-1 secretion through an in vitro study using fibroblasts (Hs68 cells) and keratinocytes (HaCaT cells). Among the three skin care foods developed in this study, three beans cookie and avocado yoghurt influenced the production of pro-collagen type I C peptide and suppressed MMP-1 secretion; however, tiger nut Galsu drink did not exhibit these effects. All skin care foods, including three beans cookie and plain yoghurt ($50{\mu}g/mL$, p<0.001) influenced the suppression of MMP-1 in addition to other commercially available breast milk production support foods examined, such as Heath Heather ($50{\mu}g/mL$, p<0.001), Happy Mama ($50{\mu}g/mL$, p<0.01), BioLys ($50{\mu}g/mL$, p<0.001), Enfamama ($25{\mu}g/mL$, p<0.0001), and Pregnagen ($25{\mu}g/mL$, p<0.001). Avocado fruit yoghurt ($25{\mu}g/mL$, p<0.05), avocado fruit jam yoghurt ($50{\mu}g/mL$, p<0.01), Enfamama ($100{\mu}g/mL$, p<0.05), and Pregnagen ($100{\mu}g/mL$, p<0.05) influenced the production of pro-collagen type I C peptide and suppressed MMP-1 secretion. This result indicates that only avocado jam yoghurt significantly influenced both the prevention of skin keratinization and acceleration of recovery of skin fibrous structure. Therefore, avocado is a favorable ingredient for nutrition-balanced dietary foods or an essential ingredient in products for revitalization of human skin.

Inhibitory Effect of Ginkgolide B on Platelet Aggregation in a cAMP- and cGMP-dependent Manner by Activated MMP-9

  • Cho, Hyun-Jeong;Nam, Kyung-Soo
    • BMB Reports
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    • 제40권5호
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    • pp.678-683
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    • 2007
  • Extracts from the leaves of the Ginkgo biloba are becoming increasingly popular as a treatment that is claimed to reduce atherosclerosis, coronary artery disease, and thrombosis. In this study, the effect of ginkgolide B (GB) from Ginkgo biloba leaves in collagen (10 ${\mu}g/ml$)-stimulated platelet aggregation was investigated. It has been known that human platelets release matrix metallo-proteinase-9 (MMP-9), and that it significantly inhibited platelet aggregation stimulated by collagen. Zymographic analysis confirmed that pro-MMP-9 (92-kDa) was activated by GB to form an MMP-9 (86-kDa) on gelatinolytic activities. And then, activated MMP-9 by GB dose-dependently inhibited platelet aggregation, intracellular $Ca^{2+}$ mobilization, and thromboxane $A_2$ ($TXA_2$) formation in collagen-stimulated platelets. Activated MMP-9 by GB directly affects down-regulations of cyclooxygenase-1 (COX-1) or $TXA_2$ synthase in a cell free system. In addition, activated MMP-9 significantly increased the formation of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), which have the anti-platelet function in resting and collagen-stimulated platelets. Therefore, we suggest that activated MMP-9 by GB may increase the intracellular cAMP and cGMP production, inhibit the intracellular $Ca^{2+}$ mobilization and $TXA_2$ production, thereby leading to inhibition of platelet aggregation. These results strongly indicate that activated MMP-9 is a potent inhibitor of collagen-stimulated platelet aggregation. It may act a crucial role as a negative regulator during platelet activation.

Collagen II로 유도된 CIA 관절염 생쥐의 대한 가미해동피산(加味海桐皮散)의 억제 효과 (Suppressive Effects of GHS in Knee Joint, Regional Lymph Nodes, and Spleen on Collagen-induced Arthritis in Mice)

  • 김남욱;김동희
    • 동의생리병리학회지
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    • 제21권5호
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    • pp.1233-1242
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    • 2007
  • Rheumatoid arthritis (RA) is a systemic autoimmune disease with chronic inflammation characterized by hyperplasia of synovial cells in affected joints, which might be mediated by the altered activation of Immune system, ultimately leading to the destruction of cartilage and bone. To examine effects of GHS on rheumatoid arthritis DBA/1J mice were immunized with bovine type II collagen to induced arthritis and then treated with GHS once a day for 7 weeks. Oral administration of GHS (200 mg/Kg) significantly suppressed the progression of CIA, which extend is comparable to that of methotrexate (MTX, 0.3 mg/Kg), a positive control. The severity of arthritis within the knee joints, which was evaluated by histological assessment of cartilage destruction and pannus formation, was also lowered by GHS. The production of TNF-and IL-6 in serum was significantly suppressed. The levels of IFN-g in the culture supernatant of splenocytes stimulated with CD3/CD28 or collagen were dramatically decreased, while those of IL-4 was increased. The levels of IgG and IgM RA factor were also decreased in the serum. FACS analysis indicated that B cells (in DLN), CD3+ T cells (in spleen, and paw joint), CD11b+Gr-1+ cells (in paw joint), CD3+CD49b(DX5) (in PBMC) were decreased and there was increased proportion of CD3+, CD4+, CD8+, CD4+CD25+ T cells in DLN. In conclusion, our results demonstrates that GHS significantly suppressed the progression of CIA and this action was characterized by the decreased production of TNF-a, IL-6, and rheumatoid factors, and modulations of immune cell populations.

Retinoic acid의 ERK 신호전달경로를 통한 nitric oxide 유도 연골세포 탈분화 심화 기작 (Retinoic Acid Potentiates Nitric Oxide-Induced Dedifferentiation through the ERK Pathway in Rabbit Articular Chondrocytes)

  • 유선미;김송자
    • 생명과학회지
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    • 제21권4호
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    • pp.534-541
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    • 2011
  • Retinoic acid (RA)는 Vitamin A의 대사산물로서 토끼 관절 연골세포의 탈분화를 유도하는 물질로 알려져 있다. 그러나 RA가 탈분화를 조절하는 정확한 메커니즘은 잘 알려져 있지 않다. 따라서, Nitric Oxide (NO)가 유도하는 탈분화에 미치는 RA의 분자적 기전에 관한 연구를 수행하였다. 그 결과, RA는 NO가 유도하는 탈분화를 촉진시키는 것을 확인 할 수 있었다. 이와 같은 결과는 Western blot analysis를 통해 연골세포 분화의 표지 단백질인 type II collagen 및 Sox-9의 발현양상을 통해 확인 할 수 있었으며, Alcian blue staining을 통해 연골세포의 기질을 구성하고 있는 단백질인 sulfated proteoglycan의 발현량을 통해서도 확인 할 수 있었다. 또한, RA는 NO 가 유도하는 ERK의 활성을 더욱 증가 시켰다. ERK의 억제자인 PD98059를 사용하여 ERK의 활성을 억제하였을 때 RA가 감소시키는 type II collagen 및 Sox-9의 발현과 sulfated proteoglycan의 생성 양상이 PD98059에 의해 다시 회복되는 것을 확인 할 수 있었다. 이러한 모든 결과를 종합해 볼 때, RA는 NO가 유도하는 탈분화를 ERK 신호전달경로를 통해 조절하는 것을 확인 할 수 있었다.

신규한 Palmitoyl Tripeptide의 피부 주름개선 효과에 관한 연구 (A Study on the Skin Anti-wrinkle Effect of Novel Palmitoyl Tripeptide)

  • 배순민;안영훈;정진교;황정근
    • 대한화장품학회지
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    • 제36권1호
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    • pp.65-69
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    • 2010
  • 콜라겐은 포유동물의 가장 풍부한 동물성 단백짙로, 전체 단백질의 약 30 %를 차지하며, 결합 조직에 존재하며 대부분의 장기의 구조적 지지에 기여한다. Tripeptide (glycine-proline-hydroxyproline: INCI name Tripeptide-29) 는 collagen type 1의 주성분이며, palmitoyl tripeptide (palmitoyl-glycine-proline-hydroxyproline: INCI name Palmitoyl Tripeptide-29) 는 콜라겐의 합성을 촉진하는 항노화 불질로서 디자인된 합성소재이다 합성된 웹타이드 유도체는 HPLC를 이용하여 분식하였다. in vitro test를 통하여 콜라겐합성과 섬유아세포 증식 효능을 확인하였고, 비침습적 기기를 사용하여 피검자에 대한 8주간의 적용결과 피부주름과 탄력의 상당한 개선을 확인하였다. Palmitoyl tripeptide는 우수한 항노화 효능을 갖는 화장품 소재로 사료된다.

Effects of Polygoni Multiflori Radix on the Elastase, and Collagenase Activities and the Procollagen Synthesis in Hs68 Human Fibroblasts

  • Kim, Myung-Gyou;Leem, Kang-Hyun
    • 대한본초학회지
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    • 제29권1호
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    • pp.7-12
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    • 2014
  • Objectives : Polygoni Multiflori Radix (PMR), the roots of Polygonum multiflorum Thunberg, is used to nourish the blood and yin and used for preventing premature greying of the hair. There are some articles on its preventing effects on the melanogenesis. However, there is no report about its effects on the collagen and elastin. The present study was designed to investigate its effects on collagen metabolism and elastase activity. Methods : The effects of PMR on type I procollagen production and collagenase activity in human normal fibroblasts Hs68 after UVB (312 nm) irradiation were measured by ELISA method. Cells were pretreated with the PMR for 24 hours prior to UVB irradiation. After UVB irradiation, cells were retreated with the sample and incubated for additional 24 hours. The amount of collagen type I was measured with a procollagen type I C-peptide assay kit. The activity of collagenase was measured with a MMP-1 human biotrak ELISA system. The elastase activities after treatment of PMR were measured as well. Results : In the present study, the collagen production was not increased. However, the increased collagenase activity after UVB damage was significantly recovered to $50.2{\pm}14.5%$, $8.2{\pm}3.1%$, and $10.0{\pm}3.3%$ (10, 30, and $100{\mu}g/ml$). The elastase activities (10, 100, and $1000{\mu}g/ml$) significantly reduced to $75.2{\pm}5.2%$, $40.3{\pm}1.2%$, and $27.0{\pm}1.9%$, respectively. Conclusion : PMR showed the inhibitory effects on collagenase and elastase activity. These results suggest that PMR may have potential as an anti-aging ingredient in cosmetic herbal treatment.

Microbial Transglutaminase Modifies Gel Properties of Porcine Collagen

  • Erwanto, Y.;Kawahara, S.;Katayama, K.;Takenoyama, S.;Fujino, H.;Yamauchi, K.;Morishita, T.;Kai, Y.;Watanabe, S.;Muguruma, M.
    • Asian-Australasian Journal of Animal Sciences
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    • 제16권2호
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    • pp.269-276
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    • 2003
  • We studied the gel properties of porcine collagen with microbial transglutaminase (MTGase) as a catalyst. A creep meter was used to measure the mechanical properties of gel. The results showed samples with high concentration of MTGase gelled faster than those with a low concentration of MTGase. The gel strength increased with incubation time and the peaks of breaking strength for 0.1, 0.2 and 0.5% MTGase were obtained at 40, 20 and 10 min incubation time, respectively. According to SDS-PAGE, the MTGase was successfully created a collagen polymer with an increase in molecular weight, whereas no change in formation was shown without MTGase. The sample with 0.5% MTGase began to polymerize after 10 or 20 min incubation at $50^{\circ}C$, and complete polymerization occurred after 40-60 min incubation. Scanning electron microscopic analysis revealed that the gel of porcine collagen in the presence of MTGase produced an extremely well cross-linked network. The differential scanning calorimetric analysis showed the peak thermal transition of porcine collagen gel was at $36^{\circ}C$, and that with MTGase no peak was detected during heating from 20 to $120^{\circ}C$. The melting point of porcine collagen gel could be controlled by MTGase concentration, incubation temperature and protein concentration. Knowledge of the structural and physicochemical properties of porcine collagen gel catalyzed with MTGase could facilitate their use in food products.

관절7호방이 Type II collagen으로 유발된 흰쥐의 관절염에 미치는 영향 (Suppressive Effect of GJB-7 on Collagen-Induced Arthritis in Mice)

  • 민부기;오민석
    • 대한한의학회지
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    • 제31권4호
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    • pp.63-78
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    • 2010
  • Objectives: This study was carried out to know the effects of Gwan-Jul-Bang-7 (hereafter referred to GJB-7) on the inhibition of arthritis induced by collagen on the mouse. Methods: To assess the effects of GJB-7 on mouse with arthritis induced by collagen II, we conducted several experiments such as analysis of cytotoxicity, hepatotoxicity, arthritis index, total cell number of draining lymph nodes and paw joints, value of immunocyte in PBMC (peripheral blood mononuclear cell), DLN (draining lymph node) and paw joint, measurement of cytokine and anti-collagen II, observation of the histological changes of joint. Results: 1. Cytotoxicity against HFC (human fibroblast cells) was not observed in any concentration and hepatotoxicity was not observed in the GJB-7 treated group. 2. The incidence of arthritis significantly decreased. 3. Total cell number of draining lymph nodes significantly increased and total cell number of paw joints significantly decreased. 4. The percentage of $CD8^+$ cells in PBMC (peripheral blood mononuclear cell) significantly increased. The percentage of $CD3^+/CD69^+$, and $CD3^+/CD49b^+$ cells in PBMC significantly decreased. 5. The percentage of $CD19^+,\;CD3^+$, and $CD4^+/CD25^+$ cells in DLN (draining lymph nodes) significantly increased. The percentage of $B220^+/CD23^+$ cells in DLN significantly decreased. 6. The percentage of $CD3^+,\;CD4^+$, and $CD11b^+/Gr-1^+$ cells in paw joints significantly decreased. 7. The production of TNF-$\alpha$, IL-6, and MCP-1 significantly decreased. 8. Anti-collagen II in serum significantly decreased. 9. With the hematoxylin and eosin stain, inflammation of joint decreased. Under Masson's trichrome stain, the cartilage destruction and synovial cell proliferation and the expression of collagen fibers decreased. Conclusions: Comparison of the results for this study showed that GJB-7 had immunomodulatory effects. So we expect that GJB-7 could be used as an effective drug for not only rheumatoid arthritis but also another auto-immune diseases.