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Related Concept Videos

Anatomy of the Heart01:27

Anatomy of the Heart

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The human heart is made up of three layers of tissue that are surrounded by the pericardium, a membrane that protects and confines the heart. The outermost layer, closest to the pericardium, is the epicardium. The pericardial cavity separates the pericardium from the epicardium. Beneath the epicardium is the myocardium, the middle layer, and the endocardium, the innermost layer. There are four chambers of the heart: the right atrium, the right ventricle, the left atrium, and the left ventricle.
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Anatomy of the Heart01:20

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The heart is a hollow, muscular organ approximately the size of a fist, consisting of four chambers. It is enclosed in the pericardium, a fibrous sac with two layers: the visceral and parietal pericardium, separated by a fluid-filled space containing serous fluid to reduce friction.
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Improving Translational Accuracy02:07

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Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
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The heart, a muscular organ located in the chest, functions as the body's pump, circulating blood through the vascular system. It has four chambers: two atria on top and two ventricles below. The right atrium receives deoxygenated blood from the body and passes it to the right ventricle, which pumps it to the lungs for oxygenation. The left atrium receives oxygenated blood from the lungs and transfers it to the left ventricle, which pumps it to the rest of the body.
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Autorhythmicity is a term that refers to the heart's inherent ability to generate electrical signals and instigate muscle contractions. This self-regulating conduction system within the heart consists of two key components: the pacemaker cells and specialized conducting cells.
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Induction of Atherosclerotic Plaques Through Activation of Mineralocorticoid Receptors in Apolipoprotein E-deficient Mice
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Tongxinluo Improves Apolipoprotein E-Deficient Mouse Heart Function.

Guo-Qiang Yuan1, Song Gao2, Yong-Jian Geng2

  • 1Department of Collateral Disease, Research Institute of Integrated Traditional Chinese Medicine and Western Medicine of Hebei, Shijiazhuang, Hebei 050035; Department of Cardiovascular Disease, Hebei Yiling Hospital, Shijiazhuang, Hebei 050091, China.

Chinese Medical Journal
|February 28, 2018
PubMed
Summary
This summary is machine-generated.

Tongxinluo (TXL) improves heart function in mice with hypercholesterolemia by reducing blood fats and enhancing vascular health. This compound increases microvascular density (MVD) in the heart, potentially through increased vascular endothelial growth factor (VEGF) expression.

Keywords:
Heart FunctionMicrovascular ProtectionTongxinluo

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Area of Science:

  • Cardiovascular Research
  • Pharmacology
  • Traditional Chinese Medicine

Background:

  • Previous studies indicated Tongxinluo (TXL) protects against myocardial ischemia-reperfusion injury and improves endothelial function.
  • Hypercholesterolemia impairs heart function by affecting artery endothelial function and reducing microvascular density (MVD).

Purpose of the Study:

  • To investigate if TXL improves hypercholesterolemia-impaired heart function in mice.
  • To determine if TXL protects artery endothelial function and increases cardiac MVD.
  • To explore the molecular mechanisms underlying TXL's cardiovascular protective effects.

Main Methods:

  • Administration of TXL to ApoE-/- mice and wild-type controls.
  • Assessment of serum lipid profiles, cardiac function (echocardiography), and aortic blood flow parameters.
  • Evaluation of endothelium-dependent vasodilation and measurement of vascular endothelial growth factor (VEGF) and myocardial CD34 expression.

Main Results:

  • TXL reduced triglyceride and VLDL levels but did not significantly alter total cholesterol.
  • TXL improved cardiac function, enhanced aortic blood flow, and improved endothelium-dependent vasodilation in ApoE-/- mice.
  • TXL treatment increased cardiac MVD and VEGF expression in ApoE-/- mice.

Conclusions:

  • TXL improves cardiac function in ApoE-/- mice through multiple pathways, including lipid reduction and enhanced vascular function.
  • TXL increases aortic blood supply capacity, vessel elasticity, and endothelium-dependent vasodilation.
  • TXL enhances cardiac MVD, potentially via increased VEGF expression, contributing to its cardioprotective effects.