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      KCI등재 SCOPUS SCIE

      Neuroimmune interactions and kidney disease

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      https://www.riss.kr/link?id=A106374168

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      다국어 초록 (Multilingual Abstract)

      The autonomic nervous system plays critical roles in maintaining homeostasis in humans, directly regulating inflammation by altering the activity of the immune system. The cholinergic anti-inflammatory pathway is a wellstudied neuroimmune interaction involving the vagus nerve. CD4-positive T cells expressing β2 adrenergic receptors and macrophages expressing the alpha 7 subunit of the nicotinic acetylcholine receptor in the spleen receive neurotransmitters such as norepinephrine and acetylcholine and are key mediators of the cholinergic antiinflammatory pathway. Recent studies have demonstrated that vagus nerve stimulation, ultrasound, and restraint stress elicit protective effects against renal ischemia-reperfusion injury. These protective effects are induced primarily via activation of the cholinergic anti-inflammatory pathway. In addition to these immunological roles, nervous systems are directly related to homeostasis of renal physiology. Whole-kidney three-dimensional visualization using the tissue clearing technique CUBIC (clear, unobstructed brain/body imaging cocktails and computational analysis) has illustrated that renal sympathetic nerves are primarily distributed around arteries in the kidneys and denervated after ischemia-reperfusion injury. In contrast, artificial renal sympathetic denervation has a protective effect against kidney disease progression in murine models. Further studies are needed to elucidate how neural networks are involved in progression of kidney disease.
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      The autonomic nervous system plays critical roles in maintaining homeostasis in humans, directly regulating inflammation by altering the activity of the immune system. The cholinergic anti-inflammatory pathway is a wellstudied neuroimmune interaction ...

      The autonomic nervous system plays critical roles in maintaining homeostasis in humans, directly regulating inflammation by altering the activity of the immune system. The cholinergic anti-inflammatory pathway is a wellstudied neuroimmune interaction involving the vagus nerve. CD4-positive T cells expressing β2 adrenergic receptors and macrophages expressing the alpha 7 subunit of the nicotinic acetylcholine receptor in the spleen receive neurotransmitters such as norepinephrine and acetylcholine and are key mediators of the cholinergic antiinflammatory pathway. Recent studies have demonstrated that vagus nerve stimulation, ultrasound, and restraint stress elicit protective effects against renal ischemia-reperfusion injury. These protective effects are induced primarily via activation of the cholinergic anti-inflammatory pathway. In addition to these immunological roles, nervous systems are directly related to homeostasis of renal physiology. Whole-kidney three-dimensional visualization using the tissue clearing technique CUBIC (clear, unobstructed brain/body imaging cocktails and computational analysis) has illustrated that renal sympathetic nerves are primarily distributed around arteries in the kidneys and denervated after ischemia-reperfusion injury. In contrast, artificial renal sympathetic denervation has a protective effect against kidney disease progression in murine models. Further studies are needed to elucidate how neural networks are involved in progression of kidney disease.

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      참고문헌 (Reference)

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      5 Inoue T, "Vagus nerve stimulation mediates protection from kidney ischemia-reperfusion injury through α7nAChR+ splenocytes" 126 : 1939-1952, 2016

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      10 Chang RB, "Vagal sensory neuron subtypes that differentially control breathing" 161 : 622-633, 2015

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      30 Kim J, "Renal nerves drive interstitial fibrogenesis in obstructive nephropathy" 24 : 229-242, 2013

      31 Nagasu H, "Renal denervation reduces glomerular injury by suppressing NAD(P)H oxidase activity in Dahl salt-sensitive rats" 25 : 2889-2898, 2010

      32 Kim J, "Renal denervation prevents long-term sequelae of ischemic renal injury" 87 : 350-358, 2015

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      42 Inoue T, "Non-canonical cholinergic anti-inflammatory pathway-mediated activation of peritoneal macrophages induces Hes1 and blocks ischemia/reperfusion injury in the kidney" 95 : 563-576, 2019

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      51 Huen SC, "Macrophage-mediated injury and repair after ischemic kidney injury" 30 : 199-209, 2015

      52 Sun P, "Involvement of MAPK/NF-κB signaling in the activation of the cholinergic anti-inflammatory pathway in experimental colitis by chronic vagus nerve stimulation" 8 : e69424-, 2013

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      58 Jang HR, "Immune cells in experimental acute kidney injury" 11 : 88-101, 2015

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      63 Hasegawa S, "Comprehensive three-dimensional analysis(CUBIC-kidney)visualizes abnormal renal sympathetic nerves after ischemia/reperfusion injury" 96 : 129-138, 2019

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      65 Saeed RW, "Cholinergic stimulation blocks endothelial cell activation and leukocyte recruitment during inflammation" 201 : 1113-1123, 2005

      66 Wang H, "Cholinergic agonists inhibit HMGB1 release and improve survival in experimental sepsis" 10 : 1216-1221, 2004

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      75 The FO, "Activation of the cholinergic anti-inflammatory pathway ameliorates postoperative ileus in mice" 133 : 1219-1228, 2007

      76 Bellinger DL, "Acetylcholinesterase staining and choline acetyltransferase activity in the young adult rat spleen : lack of evidence for cholinergic innervation" 7 : 191-204, 1993

      77 Rosas-Ballina M, "Acetylcholine-synthesizing T cells relay neural signals in a vagus nerve circuit" 334 : 98-101, 2011

      78 Matteoli G, "A distinct vagal anti-inflammatory pathway modulates intestinal muscularis resident macrophages independent of the spleen" 63 : 938-948, 2014

      79 Carnevale D, "A cholinergicsympathetic pathway primes immunity in hypertension and mediates brain-to-spleen communication" 7 : 13035-, 2016

      80 Zhao Z, "A central catecholaminergic circuit controls blood glucose levels during stress" 95 : 138-152, 2017

      81 Aaronson ST, "A 5-year observational study of patients with treatment-resistant depression treated with vagus nerve stimulation or treatment as usual : comparison of response, remission, and suicidality" 174 : 640-648, 2017

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      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-11-29 학술지명변경 한글명 : The Korean Journal of Nephrology -> Kidney Research and Clinical Practice
      외국어명 : 미등록 -> Kidney Research and Clinical Practice
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      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-02-22 학술지명변경 한글명 : 대한신장학회지 -> The Korean Society of Nephrology KCI등재
      2007-02-22 학술지명변경 한글명 : 대한신장학회지 -> The Korean Journal of Nephrology KCI등재
      2005-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2004-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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