The blood–saliva barrier (BSB) is a biological barrier that consists of the epithelial cell layers of the oral mucosa and salivary glands, and provides physiological separation between blood vessels and the saliva in the oral cavity.[1][2] In Russian academic literature the barrier is usually called the hematosalivary or hematosalivarian barrier.[3][2]
The blood–saliva barrier is a protective mechanism that helps maintain the integrity and stability of the blood and prevents the exchange of certain substances between the bloodstream and saliva, such as electrolytes,[5] small-molecular-weight proteins, metabolic products, and specific/non-specific defense factors.[4][1][2]
The blood–saliva barrier also plays a role in immune defense mechanisms within the oral cavity. Immune cells, such as macrophages and lymphocytes, are contained within the connective tissue layer beneath the barrier.
Salivary glands are well-perfused organs due to the presence of numerous arterio-venous anastomoses[6] with sphincters. When these sphincters close, they increase the pressure in the capillaries of salivary glands, facilitating the movement of various metabolites from the capillary lumen into secretory epithelial cells for saliva formation. Salivary glands exhibit high selectivity in their activity, confirming the functioning of the barrier which regulates its permeability in response to physiological or pathological changes within the body. Substance entry through the barrier mainly occurs via simple passive diffusion (paracellular),[5][2] active transport, or endocytosis, primarily determined by lipophilicity, charge, and size of substances being transported. Proteinaceous substances are thought to be primarily transported across the mucosa via a paracellular mechanism facilitated by passive diffusion.[2]
The blood–saliva barrier changes permeability under the influence of the autonomic nervous system and humoral factors.[2]
Clinical significance
In vitro models of the blood–saliva barrier are used to investigate and understand the transport of salivary biomarkers from blood to saliva.[7][1]
The ability of blood–saliva barrier of preventing the transport of certain molecules from blood to saliva while allowing the transport of the other has a practical application in measuring levels of steroids which are unbound ("free") and have biological activity. An example of such molecule is cortisol, which is lipophilic, and is transported bound to transcortin (also known as corticosteroid-binding globulin) and albumin, while only a small part of the total serum cortisol is unbound and has biological activity.[8] This binding of cortisol to transcortin is accomplished through hydrophobic interactions in which cortisol binds in a 1:1 ratio.[9] Serum cortisol assays measure total cortisol, and such results may be misleading for patients with altered serum protein concentrations. The salivary cortisol test avoids this problem because only free cortisol can pass through blood–saliva barrier[10][11][12][13] due to the fact that transcortin particles are too large to pass through the barrier.[14][1]
History
A key milestone in the study of the blood–saliva barrier in medicine was reached when SovietphysiologistLina Stern introduced the concept of "histohematological barriers" in 1929, highlighting their plasticity and their ability to regulate internal environment homeostasis through interactions with exogenous and endogenous physiological compounds.[2] While working at the University of Geneva, Stern published a series of studies demonstrating the existence of the blood–brain barrier with colleague Raymond Gautier.[15][16][17] In a 1934 paper, Stern also introduced the notions of barrier selectivity and barrier resistance, realizing that the blood–brain barrier both selectively allows certain substances to enter the brain and protects the internal milieu of the brain from that of the blood.[18] The study of the blood–brain barrier contributed to the subsequent studies of the other anatomical barriers. A significant place in understanding of the barrier mechanisms is occupied by the placental barrier, which exists between maternal blood and fetal tissues. Following extended research, the blood–saliva barrier was described for the first time in 1977[19] by a Soviet physician Yurii Alexandrovich Petrovich[20] as "hematosalivary barrer".[2]
Research directions
In recent years, significant progress has been made in studying different aspects blood–saliva barrier function using advanced tools such as molecular biology techniques, confocal microscopy, immunofluorescence staining methods, and transcellular migration assays. These studies elucidate cellular interactions involved in creating tight junctions[5][2] between endothelial cells lining capillaries within salivary glands.[2]
Furthermore, experimental models utilizing cell cultures have demonstrated potential applications for tissue engineering approaches aimed at developing artificial salivary glands or improving treatments for conditions associated with reduced salivation.[2]
^Ulanova EA, Grigor'ev IV, Novikova IA (2001). "[Hematosalivary mechanisms of regulation in rheumatoid arthritis]". Ter Arkh (in Russian). 73 (11): 92–4. PMID11806220.
^Granger DA, Hibel LC, Fortunato CK, Kapelewski CH (November 2009). "Medication effects on salivary cortisol: tactics and strategy to minimize impact in behavioral and developmental science". Psychoneuroendocrinology. 34 (10): 1437–48. doi:10.1016/j.psyneuen.2009.06.017. PMID19632788. S2CID3100315.
^Lane J (2006). "Can non-invasive glucocorticoid measures be used as reliable indicators of stress in animals?". Animal Welfare. 15 (4): 331–342. doi:10.1017/S0962728600030657. S2CID80026053.
