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Myasthenia Gravis

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Myasthenia Gravis

● Symptomata et causas  

Myasthenia gravis (MG) est perturbatio autoimmune chronica in qua elementorum communicationem inter nervos et musculum destruunt, inde in debilitate musculorum sceleti. Myasthenia gravis musculos voluntarios corporis afficit, praesertim eos qui oculos, os, fauces et membra moderantur. Morbus aliquem quavis aetate percutere potest, sed frequentius cernitur in iuvenibus (20 et 30 annis) et viris 50 senioribus etatis.

Myasthenia gravis non hereditaria et non contagiosa est. Plerumque postea in vita oritur cum elementorum in corpore impetum normales receptores in musculus. Hoc impedit opus chemicum ad contractionem musculi incitandam.

fimmu-11-00776-9

Autoimmune Pathologia in Myasthenia Gravis Morbus Subtypes a Mechanismis Immunopathologiae divergentibus gubernatur. Frontem. Immunol., 27 Maii 2020 .


 ● exempla in loco 【Date➡models】

R97-116 peptides inductae MG Model

【Mechanism】Myasthenia gravis (MG) est anticorpus mediatum, T cellae-dependens, complementum cum autoimmune morbo implicatum, proprium detrimentum acetylcholini receptoris (AChR) in membrana postsynaptica commissurae neuromuscularis et effecta in transmissione neuromusculari et debilitate musculi. Experimentalis autoimmune myasthenia gravis (EAMG) in Ludovicum mures induci potest ab immunizatione cum torpedo acetylcholino receptore (TAchR) vel synthetica peptide respondens regioni 97-116 rat AChR α subunita (R97-116 peptide), quod est certum exemplar pro MG humanis et aptum ad investigandam progressionem novae therapeuticae. 

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MG模型介绍 20240204_20240613114124





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