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Update in Critical Care Medicine - Nervous system: Metabolic syndrome in astrocyte injury - cellular and molecular implications Kar-Lok Wong MD, PhD, FICS.

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Presentation on theme: "Update in Critical Care Medicine - Nervous system: Metabolic syndrome in astrocyte injury - cellular and molecular implications Kar-Lok Wong MD, PhD, FICS."— Presentation transcript:

1 Update in Critical Care Medicine - Nervous system: Metabolic syndrome in astrocyte injury - cellular and molecular implications Kar-Lok Wong MD, PhD, FICS 黃家樂 醫生 博士 教授 Director & Professor Department of Anesthesiology Institute of Clinical Medical Science China Medical University & Hospital, Taichung, Taiwan Honorary Professor LKS Faculty of Medicine, University of Hong Kong, Hong Kong Visiting Professor Shandong Medical University, Shandong, China Taishan Medical University, Taian, Shandong, China Director Laboratory Animal Center China Medical University & Hospital Taichung, Taiwan

2 Introduction Metabolic syndrome (MS) is quite common. Approximately 20%-30% of the population in industrialized countries have MS By the year 2010, the MS is expected to affect 50-75 million people in the US alone (Ford 2002). In Taiwan, MS is present in more than 30% of the Taiwan adult population aged 40 years and over in a metropolitan area Pan et al has been reported that; for most BMI values, the prevalence of hypertension, diabetes, and hyperuricemia were higher for Taiwanese than for US whites. BMI-comorbidity relations were stronger in Taiwanese than in US blacks for all comorbidities studied (Pan 2004). It has become a significant health problem in Taiwan, but the resource injected by the government seems insufficient to deal with this difficult issue in the future.

3 Men with the MS as defined by the NCEP criteria (National Cholesterol Education Program Adult Treatment Program III) had a 2.05-fold risk for all strokes and 2.41-fold risk for ischemic stroke. The etiologic fraction estimates suggest that elimination of the MS would result in a 19% reduction in overall stroke. ( Kurl 2006, Boden-Albala 2008).Boden-Albala Prevention of the MS presents a great challenge for clinicians with respect to coronary heart disease and stroke.coronary heart disease

4 Metabolic syndrome (MS) encompasses a group of problems which will put a person at a high risk of developing cardiovascular diseases, including heart attack and stroke (Circulation. 2004; 109: 433) Effective prevention or treatment of MS significantly reduces the risk for developing serious complications. (Circulation. 2004; 109: 433) Palmitic acid (PA) is a saturated fatty acid, when being excessive, is a significant risk factor for development of MS or stroke. However, damage by MS to astrocytes is relatively unexplored. Catechin is an effective antioxidant which would be beneficial to neurons subjected to reactive oxygen species (ROS) damage as well as on cardiovascular diseases. (Circulation Research, 2010;107:1167) This study was to identify the mechanism(s) of PA-induced cytotoxicity in rat astrocytes and also to assess the protective effects of catechin.

5 Functional Roles of Astrocytes Blood-Brain Barrier Glucose metabolism – store glucose as glycogen/ ATP Maintenance of the extracellular environment – Clearance excessive glutamate Regulate neurogenesis, gliogenesis, neuroprotective (Alfonso et al., 2006; Pellerin, 2005; Walz, 2000Prat et al., 2001)

6 Functional Roles of Astrocyte (Allen & Barres, 2009)

7 Polyphenolic Catechins Polyphenols Family Anti- oxidative effect : ROS ↓, and NADPH scavenger Anti-inflammation Aging, Parkinson disease (PD), Alzheimer’s disease (AD), Stroke, Cardiovascular disease, obesity, diabetes, cancers… (Zaveri, 2005) Green Tea

8 Aims 1.To investigate the lipotoxic mechanism of PA in astrocyte. 2.To examine whether catechin can protect astrocyte from PA- induced lipotoxicity.

9 1. PA- induced concentration- dependent astrocytes death protected by catechin

10 3. PA-induced cell death was abrogated by ascorbic acid but not by salubrinal * # *

11 Palmitic Acid Cell Death ER stress: JNK, Chop, p-eIF2, Ca 2+ MMP: Cyt C, Bax, p-38 MAPK, Glucose uptake NADPH or Lipoxygenase: Apocynin, AA- 861

12 ROS Reactive Oxygen Species: – Superoxide (O2 - ) – Peroxynitrite (ONOO - ) – Hydrogen Peroxide (H 2 O 2 ) – Hydroxyl Radical (∙OH) (Hoot, 2005; Minicis & Brenner, 2007; Schramm et al., 2012; Trachootham et al., 2009)

13 Control 50 µm Control 50 µm A CH x 30 min 50 µm B PA + CH 30 min 50 µm D PA x30 min 50 µm C 4. PA-elicited ROS formation was prevented by catechin and rotenone.

14 Cell Death ( Mann, 2006; Verfaillie et al., 2012)

15 Cell Death ER stress: JNK, Chop, p-eIF2, Ca 2+ MMP: Cyt C, Bax, p-38 MAPK, Glucose uptake NADPH or Lipoxygenase: Apocynin, AA- 861 Palmitic Acid

16 (Cited from: http:// www.med.monash.edu.au)

17 Conclusions PA-induced apoptotic death of astrocytes : appeard to be unrelated to Ca 2+ elevation, Ca 2+ store depletion and ER stress resulted from ROS formation and mitochondrial potential collapse could be prevented by catechin, through inhibition on ROS generation and protection on mitochondrial functional integrity

18 Conclusion Our results demonstrated that PA-induced cytotoxicity in astrocyte could be prevented by catechin through inhibition of ROS generation and protection on mitochondrial functional integrity This study delivers important new insight in the molecular pathways that may contribute to the protective effects of catechin on astrocyte in metabolic syndrome


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