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Renal protective effects of adenosine monophosphate protein kinase (AMPK) activators in renal fibrosis and acute kidney injury model : 신장 섬유증 및 급성 신장 손상 모델에서 adenosine monophosphate protein kinase (AMPK) 활성화 인자의 신기능 보호 효과
AMPK mediated pathways in renal disease

DC Field Value Language
dc.contributor.advisor유경상-
dc.contributor.authorTsogbadrakh Bodokhsuren-
dc.date.accessioned2019-10-21T03:18:05Z-
dc.date.available2019-10-21T03:18:05Z-
dc.date.issued2019-08-
dc.identifier.other000000156655-
dc.identifier.urihttps://hdl.handle.net/10371/162266-
dc.identifier.urihttp://dcollection.snu.ac.kr/common/orgView/000000156655ko_KR
dc.description학위논문(박사)--서울대학교 대학원 :의과대학 의과학과,2019. 8. 유경상.-
dc.description.abstractAdenosine monophosphate protein kinase (AMPK)는 중요한 세포 에너지 센서이다. AMPK는 전신 수준에서 신진 대사 에너지 균형을 조절한다. AMPK 활성화가 미치는 영향은 당 및 지질대사, 사이토카인 생성 및 염증 조절, 그리고 세포 증식과 세포사멸에 이르러 그 범위가 방대하다. 본 연구자는 대표적 AMPK 활성제인 HL156A가 생체 내, 생체 밖 모델에서 신장 섬유화증에 억제 효과가 있는지 연구하였다. 또한 또 다른 AMPK 활성제인 AMP-kinase activator 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) 가 cisplatin 에 의한 급성 신손상 설치류 모델에서 보호효과가 있는지 여부를 연구 하였다. 본 연구자는 HL156A, metformin, AICAR 처리 시 AMPK 활성증가 정도를 비교 하였고, 이중 HL165A 가 가장 강력한 AMPK 활성제임을 발견 하였다. 본 연구는 AMPK 활성제가 신장 섬유증과 급성 신손상에 보호효과가 있음을 입증 하였다.
본 연구 결과 중 일부를 다음 논문에 게재 하였다:
 Tsogbadrakh, B., et al. (2018). "HL156A, a novel pharmacological agent with potent adenosine-monophosphate-activated protein kinase (AMPK) activator activity ameliorates renal fibrosis in a rat unilateral ureteral obstruction model." PLoS One 13(8): e0201692.
 Tsogbadrakh, B., et al. (2019). "AICAR, an AMPK activator, protects against cisplatin-induced acute kidney injury through the JAK/STAT/SOCS pathway." Biochem Biophys Res Commun 509(3): 680-686.
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dc.description.abstractAdenosine monophosphate protein kinase (AMPK) is a crucial cellular energy sensor. AMPK regulates metabolic energy balance at the whole body level. AMPK activation effect is diverse and include glucose and lipid metabolism, cytokine production and inflammation regulation, and cell proliferation and apoptosis. Here, the effects of a novel AMPK activator HL156A, on the inhibition of renal fibrosis in in vivo and in vitro models were examined. Also, it was investigated whether the AMP-kinase activator 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) protects against cisplatin induced acute kidney injury. The AMPK-activator activities of AICAR, metformin, and HL156A were compared in a rodent renal tubular epithelial cell line. Among the three AMPK activator substances, AMPK activation was the most potent in the presence of the HL156A molecule. Taken together, AMPK activators ameliorated renal fibrosis and acute kidney injury.
Parts of the results in this thesis have been published in the following papers:
 Tsogbadrakh, B., et al. (2018). "HL156A, a novel pharmacological agent with potent adenosine-monophosphate-activated protein kinase (AMPK) activator activity ameliorates renal fibrosis in a rat unilateral ureteral obstruction model." PLoS One 13(8): e0201692.
 Tsogbadrakh, B., et al. (2019). "AICAR, an AMPK activator, protects against cisplatin-induced acute kidney injury through the JAK/STAT/SOCS pathway." Biochem Biophys Res Commun 509(3): 680-686.
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dc.description.tableofcontentsTable of Contents
Abstract . i
Contents . iii
List of Figures . vi
List of Tables viii
Chapter 1. General Introduction 1 1
1.1. Background . 1
1.2. Purpose of this study 4
Chapter 2. HL156A activator ameliorates renal fibrosis 5
2.1. Background . 5
2.2. Materials and methods 7
2.2.1. AMPK activity. 7
2.2.2. Animal model of unilateral ureteral obstruction 8
2.2.3. Histology 9
2.2.4. Cell culture and experimental treatments 10
2.2.5. Reverse transcription-polymerase chain reaction (RT-PCR)
analysis 11
2.2.6. Western blot analysis . 12
2.2.7. Immunofluorescence staining and confocal microscopy . 14
2.2.8. Statistical analysis 14
2.3. Results . 14
2.3.1. AMPK activator activity of AICAR, metformin and
HL156A . 14
2.3.2. Animal model of unilateral ureteral obstruction 16
2.3.3. HL156A ameliorated the histological changes of renal
fibrosis induced by UUO . 17
2.3.4. HL156A ameliorated the fibrogenic signals induced by
UUO 19
2.3.5. Optimal dose and exposure time of TGF-β1 in cultured rat
proximal cell line . 23
2.3.6. HL156A up-regulated AMPK and inhibited fibrogenic signals
from NRK52E cells 25
2.3.7. The expression of inflammatory chemokine 29
2.3.8. Immunofluorescence analysis of AMPK and Smad 3
pathway 30
2.4. Discussion . 32
Chapter 3. AICAR, an AMPK activator, protects against cisplatin induced acute kidney injury 36
3.1. Background 36
3.2. Materials and Methods 38
3.2.1. Animal model and experimental design 38
3.2.2. Histological analysis 39
3.2.3. Immunohistochemistry 39
3.2.4. Cell culture and experimental treatments 40
3.2.5. Western blot analysis 41
3.2.6 Measurement of intracellular reactive oxygen species (ROS)
production 42
3.2.7. Data analyses . 42
3.3. Results 43
3.3.1. AICAR protects against cisplatin-induced AKI 43
3.3.2. AICAR effect on the renal tissue and AKI index . 44
3.3.3. AICAR effect on the renal AMPK expression in AKI . 45
3.3.4. AICAR on JAK/STAT/SOCS signaling pathway in vivo 46
3.3.5. AICAR on reactive oxygen species (ROS) in AKI . 48
3.3.6. AICAR on JAK/STAT/SOCS signaling pathway in NRK-52E
cells . 48 3.3.7. AICAR on oxidative stress markers in AKI . 50
3.4. Discussion . 51
Chapter 4. General Discussion and Conclusion 55
Bibliography 57
Abstract in Korean 65
List of Figures
Figure 2.1. Comparison of AMPK activator activities 15
Figure 2.2. The effect of HL156A treatment on UUO . 16
Fig 2.3. HL156A ameliorated histopathological changes associated with UUO. 18
Fig 2.4. Effects of HL156A treatment on mRNA and protein
expression 20
Figure 2.5. Quantitative real-time PCR for various gene expressions in the kidney tissue . 22
Fig 2.6. Pilot study to estimate the optimal dose and duration of TGF-β1 treatment . 24
Figure 2.7. The effect of HL156A on TGF-1-treated NRK52E cells 26
Figure 2.8. Quantitative real-time PCR for various gene expressions in the NRK52E cells 28
Figure 2.9. The expression of inflammatory cytokine . 29
Figure 2.10. Immunofluorescence analysis of AMPK and Smad3 pathways 31
Figure 2.11. Cleaved Caspase 3 expression in vivo and in vitro . 32
Figure 3.1. Dose dependent study in in vitro
Figure 3.2. AICAR protected against cisplatin induced AKI . 43
Figure 3.3. AICAR supplement decreased cisplatin induced AKI . 44
Figure 3.4. AICAR in p-AMPK and KIM1 expression on the rat kidney . 45
Figure 3.5. AICAR activity of the JAK/STAT signaling pathway on rat kidney . 47
Figure 3.6. AICAR on reactive oxygen species (ROS) in AKI . 48
Figure 3.7. AICAR activity of the JAK/STAT signaling pathway on NRK-52E cells . 49
Figure 3.8. AICAR on oxidative stress markers in AKI . 50
List of Tables
Table 2.1. Body weight parameters and kidney weight results 10 days after unilateral ureteral obstruction 9
Table 2.2. Primer sequences for reverse transcription PCR 11
Table 2.3. Primer sequences for quantitative real time PCR 12
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dc.language.isoeng-
dc.publisher서울대학교 대학원-
dc.subjectadenosine monophosphate protein kinase (AMPK)-
dc.subject5-aminoimidazole-4-carboxamide ribonucleotide (AICAR)-
dc.subjectunilateral ureteral obstruction (UUO)-
dc.subjectacute kidney injury (AKI)-
dc.subjectjanus kinase (JAK)-
dc.subjectsignal transducer and activator of transcription (STAT)-
dc.subject.ddc610.72-
dc.titleRenal protective effects of adenosine monophosphate protein kinase (AMPK) activators in renal fibrosis and acute kidney injury model-
dc.title.alternative신장 섬유증 및 급성 신장 손상 모델에서 adenosine monophosphate protein kinase (AMPK) 활성화 인자의 신기능 보호 효과-
dc.typeThesis-
dc.typeDissertation-
dc.contributor.AlternativeAuthor버트허수렌-
dc.contributor.department의과대학 의과학과-
dc.description.degreeDoctor-
dc.date.awarded2019-08-
dc.title.subtitleAMPK mediated pathways in renal disease-
dc.contributor.major의과학과-
dc.identifier.uciI804:11032-000000156655-
dc.identifier.holdings000000000040▲000000000041▲000000156655▲-
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