Circulating antibodies against rat parotid gland M(3) muscarinic receptors in primary Sjogren's syndrome

In this study we demonstrate that IgG present in the sera of patients with primary Sjogren's syndrome (PSS) could bind and activate muscarinic acetylcholine receptors (mAChRs) of rat parotid gland. These antibodies were able to inhibit in a non-competitive manner the binding of H-3-quinuclidinyl benzilate (QNB) to mAChRs of purified rat parotid gland membranes. Moreover, IgG from PSS could modify biological effects mediated by mAChR activation; i.e. decrease cAMP, increase phosphoinositide turnover without affecting cGMP. Atropine and 4-DAMP blocked all of these effects, and carbachol mimicked them, confirming the M(3) subtype mAChRs mediated PSS IgG action. Neither binding nor biological effect were obtained with Ige From sera of normal women. The prevalence of cholinergic antibody was 100% in PSS, and was independent of Ro/SS-A and La/SS-B antibodies. Ir could be concluded that antibody against mAChRs mag. be another scrum factor to be considered in the pathophysiology of the development of PSS.