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Is the probable spillage of the lung surfactant dipalmitoylphosphatidylcholine the ultimate source of diabetes type 1?
Arieli, Ran; Khatib, Soliman; Khattib, Aatef; Bukovetzky, Elena; Gottfried, Orna Dally.
Afiliación
  • Arieli R; The Israel Naval Medical Institute (INMI), Haifa, Israel; Eliachar Research Laboratory, Western Galilee Medical Center, Nahariya, Israel. Electronic address: arieli1940@gmail.com.
  • Khatib S; Department of Natural Compounds and Analytical Chemistry, MIGAL - Galilee Research Institute, Israel; Laboratory of Analytical Chemistry, Tel Hai College, Kiryat Shmona, Israel.
  • Khattib A; Department of Pediatrics, Ziv Medical Center, Safed, Israel.
  • Bukovetzky E; Biochemistry Laboratory, Ziv Medical Center, Safed, Israel.
  • Gottfried OD; Department of Pediatrics, Ziv Medical Center, Safed, Israel; Azrieli Faculty of Medicine, Bar Ilan University, Safed, Israel; Pediatric Outpatient Clinic and Diabetes, Ziv Medical Center, Safed, Israel.
Respir Physiol Neurobiol ; 286: 103615, 2021 04.
Article en En | MEDLINE | ID: mdl-33421610
ABSTRACT
The lung surfactant dipalmitoylphosphatidylcholine (DPPC) most probably leaks into the blood, settling on the luminal aspect of blood vessels to create active hydrophobic spots (AHS). Nanobubbles are formed at these spots from dissolved gas. We hypothesized that when a large molecule in the blood comes into contact with a nanobubble at the AHS, its tertiary structure is disrupted. An epitope not previously having undergone thymus education may then prompt an autoimmune response. There are thus two independent processes which may share the blame for autoimmune disease spillage of large molecules into the blood, and the creation of AHS. DPPC was measured in 10 diabetes type 1 patients and 10 control subjects. DPPC in the diabetic group was 4.63 ± 0.68 µg/mL, non-significantly higher than in the control group (4.23 ± 0.94 µg/mL). However, in the diabetic group, DPPC was high when the samples were taken within 1.5 years of disease onset. This is closer to the time of AHS production, which takes place ahead of the disease. Further investigation, with sampling for DPPC as soon as possible after onset of the disease, may provide additional support for our hypothesis. If proved true, this may open up considerable therapeutic potential.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tensoactivos / 1,2-Dipalmitoilfosfatidilcolina / Diabetes Mellitus Tipo 1 / Interacciones Hidrofóbicas e Hidrofílicas / Pulmón Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Respir Physiol Neurobiol Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tensoactivos / 1,2-Dipalmitoilfosfatidilcolina / Diabetes Mellitus Tipo 1 / Interacciones Hidrofóbicas e Hidrofílicas / Pulmón Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Respir Physiol Neurobiol Año: 2021 Tipo del documento: Article