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dc.identifier.urihttp://hdl.handle.net/1951/55474
dc.identifier.urihttp://hdl.handle.net/11401/72543
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.en_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dc.typeDissertation
dcterms.abstractTear secretion is a complicated process that involves two different cell types. The lacrimal acinar cell is thought to secrete a hypertonic primary fluid with a high K<super>+</super> concentration. This fluid is then modified by the ductal epithelia and transported to the avascular ocular surface. It is known that both sympathetic and parasympathetic input trigger protein release, but the role of adrenergic stimulation on water secretion in lacrimal gland remains unclear. Therefore, the first goal of this dissertation is to examine the influence of&#913;- and&#914;-adrenergic activation on tear fluid production.Tear secretion requires coordination of different membrane channels and transporters. Walcott et al. showed the importance of basolateral Na<super>+</super>-K<super>+</super>-2Cl<super>-</super>-cotransporter (NKCC1) on secretion rate. The second goal is to develop an acinar cell mathematical model with cell volume regulation. The model is used to examine whether NKCC1 alone is sufficient to generate hypertonic tear fluid with high KCl content when the cell is stimulated. Subsequently the model was expanded with acid-base regulatory transporters to investigate the interaction between volume- and pH-regulation systems. This effort led to the discovery that the sodium-bicarbonate transporter is expressed in lacrimal gland and participates in tear production.Lastly, since acinar and duct cells express same membrane channels and transporters, it is likely that duct cells secrete a hypertonic fluid like acinar cell. The third goal of this project is to develop a duct cell model and combine it with the acinar cell model. The combined model was used to examine the flow dependence of tear composition. The predictions agree with measurements made in anesthetized rats.
dcterms.available2012-05-15T18:04:09Z
dcterms.available2015-04-24T14:52:34Z
dcterms.contributorPeter R. Brinken_US
dcterms.contributorSmolka, Scott A.en_US
dcterms.contributorChris Clausenen_US
dcterms.contributorGrosu, Raduen_US
dcterms.contributorPeter Reinach.en_US
dcterms.creatorHuang, Wei Chieh
dcterms.dateAccepted2012-05-15T18:04:09Z
dcterms.dateAccepted2015-04-24T14:52:34Z
dcterms.dateSubmitted2012-05-15T18:04:09Z
dcterms.dateSubmitted2015-04-24T14:52:34Z
dcterms.descriptionDepartment of Physiology and Biophysicsen_US
dcterms.formatMonograph
dcterms.formatApplication/PDFen_US
dcterms.identifierHuang_grad.sunysb_0771E_10263.pdfen_US
dcterms.identifierhttp://hdl.handle.net/1951/55474
dcterms.identifierhttp://hdl.handle.net/11401/72543
dcterms.issued2010-08-01
dcterms.languageen_US
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dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectBiology, Physiology
dcterms.subjectLacrimal Gland, Mathematical Model, Water and Electrolyte Secretion
dcterms.titleWater and Ion Transport in Lacrimal Gland: Models and Experiment
dcterms.typeDissertation


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