Myocardial lysosomes in experimental atrial septal defects.

نویسندگان

  • C A Kottmeier
  • M W Wheat
چکیده

Preliminary observations in patients undergoing open-heart surgery have suggested that the lysosomes in the right atrium are increased in patients with atrial septal defects. This increase in lysosomes per myocardial cell appears to be directly related to the size of the left to right shunt. The following experiments were performed to see if similar findings could be produced in an experimental model. Atrial septal defects were produced in seven dogs. The biopsy specimens were prepared for ultrastructural examination and viewed with an electron microscope. Lysosomes were counted in representative sections and an estimate of the lysosomes per square micron of heart tissue obtained. The number of lysosomes per square micron of myocardium increased significantly following the creation of atrial septal defects in dogs, with the most marked increase occurring in the right ventricle. Several small atrial septal defects closed spontaneously, as proved by cardiac catheterization, and in these animals the elevated lysosome counts present initially returned toward normal after obliteration of the left to right shunt at the atrial level. Control dogs showed no significant increase in myocardial lysosomes over the 18-month period despite repeated thoracotomies and myocardial biopsy. These studies add further evidence to support the role of the lysosome as an important intracellular organelle which is related to cellular stress. ADDITIONAL

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Holt-Oram Syndrome: A Rare Variant

Holt-Oram syndrome is an autosomal dominant disorder, characterised by skeletal abnormalities of the upper limb associated with congenital heart defect, mainly atrial and ventricular septal defects. Skeletal defects exclusively affect the upper limbs in the preaxial radial ray distribution and are bilateral and asymmetrical. They range from clinodactyly, absent or digitalised thumb, hypoplastic...

متن کامل

Right ventricular infarction complicated by right to left shunting through an atrial septal defect: successful treatment with an Amplatzer septal occluder.

A 68 year old woman presented with right ventricular myocardial infarction complicated by refractory hypoxaemia. She was found to have a significant right to left shunt at the atrial level through a previously undiagnosed ostium secundum atrial septal defect. Percutaneous closure of the atrial septal defect with an Amplatzer septal occluder resulted in prompt improvement in her oxygenation and ...

متن کامل

Evaluation of Clinical Course in Children and Adolescents with Atrial Septal Defects

Background Atrial septal defects (ASDs) are the most common third congenital heart defects. This study aimed to evaluate the clinical course of ASDs and the relationship between its complications, location closure and size. Materials and Methods: This cross-sectional study was conducted...

متن کامل

Isovolumic contraction acceleration before and after percutaneous closure of atrial septal defects

AIM To compare systemic right ventricular function by isovolumic myocardial acceleration before and 6 months after the percutaneous closure of atrial septal defects (ASD). MATERIAL AND METHODS Patients admitted to our tertiary center for the percutaneous closure of atrial septal defects between January 2010 and August 2012 constituted the study group. Right ventricular function of patients wa...

متن کامل

Rare case of myocardial infarction in a 19-year-old caused by a paradoxical coronary artery embolism.

This case focuses on a 19-year-old man who developed an inferior ST-segment elevation myocardial infarction as a result of a previously undetected large atrial septal defect. This cardiac anomaly facilitated the transport of a paradoxical embolism that occluded the right coronary artery.

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Circulation research

دوره 21 1  شماره 

صفحات  -

تاریخ انتشار 1967