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Mucositis

Diarrhea is a common problem that is usually self-limiting and of short duration. Increased accumulations of small intestinal and colonic contents are known to be responsible for producing diarrhea. The former may be caused by increased intestinal secretion which may be enterotoxin-induced, eg, cholera and E. col] or hormone and dmg-induced, eg, caffeine, prostaglandins, and laxatives decreased intestinal absorption because of decreased mucosal surface area, mucosal disease, eg, tropical spme, or osmotic deficiency, eg, disaccharidase or lactase deficiency and rapid transit of contents. An increased accumulation of colonic content may be linked to increased colonic secretion owing to hydroxy fatty acid or bile acids, and exudation, eg, inflammatory bowel disease or amebiasis decreased colonic absorption caused by decreased surface area, mucosal disease, and osmotic factors and rapid transit, eg, irritable bowel syndrome. [Pg.202]

Allergic Seasonal or Perennial Rhinoconjunctivitis. Histamine can cause all pathologic features of allergic rhinitis (35—37), with the exception of late-phase inflammatory reactions. Pmritus is caused by stimulation of receptors on sensory nerve endings prostaglandins (qv) may also contribute. Sneering, like pmritus, is an H -mediated neural reflex and can also be mediated by eicosanoids. Mucosal edema, which manifests as nasal... [Pg.141]

Calcium is absorbed from the intestine by facilitated diffusion and active transport. In the former, Ca " moves from the mucosal to the serosal compartments along a concentration gradient. The active transport system requires a cation pump. In both processes, a calcium-binding protein (CaBP) is thought to be required for the transport. Synthesis of CaBP is activated by 1,25-DHCC. In the active transport, release of Ca " from the mucosal cell into... [Pg.376]

Iron. The total body content of iron, ie, 3—5 g, is recycled more efficientiy than other metals. There is no mechanism for excretion of iron and what Httie iron is lost daily, ie, ca 1 mg in the male and 1.5 mg in the menstmating female, is lost mainly through exfoHated mucosal, skin, or hair ceUs, and menstmal blood (74—76). Common food sources rich in iron and other trace elements are Hsted in Table 10. [Pg.381]

SCE protects mice from G1 death after kradiation and increases the number of surviving mucosal crypt stem cells (186) in a manner similar to lL-1. [Pg.495]

Dactinomycin, an antineoplastic dmg, was discovered in 1943 and is made in rather pure form by StreptomjcesparvuUus. Dactinomycin has some bacteriostatic antibacterial and antifungal activity, but high toxicity limits its use to antineoplastic therapy. It may be used alone or with other antineoplastics, with or without surgery and synergistic x-ray therapy. Dose limiting bone marrow toxicity may result in low white cell and platelet count. Intestinal mucosal damage also occurs. Reviews of more detailed chemotherapeutic information are available (217—222). [Pg.157]

Oral mucosal membranes provide a port for systemic therapy as weU. Nitroglycerin sublingual tablets (Nitrostat) abort acute mgina attacks methyl-testosterone [58-18-4] buccal tablets (Android 5) are indicated for testosterone [58-22-0] replacement therapy (39) md nicotine [54-11-5] gum (Nicorette) aids in smoking cessation. [Pg.141]

Fiber components are the principal energy source for colonic bacteria with a further contribution from digestive tract mucosal polysaccharides. Rate of fermentation varies with the chemical nature of the fiber components. Short-chain fatty acids generated by bacterial action are partiaUy absorbed through the colon waU and provide a supplementary energy source to the host. Therefore, dietary fiber is partiaUy caloric. The short-chain fatty acids also promote reabsorption of sodium and water from the colon and stimulate colonic blood flow and pancreatic secretions. Butyrate has added health benefits. Butyric acid is the preferred energy source for the colonocytes and has been shown to promote normal colonic epitheUal ceU differentiation. Butyric acid may inhibit colonic polyps and tumors. The relationships of intestinal microflora to health and disease have been reviewed (10). [Pg.70]

The use of a bioadhesive, polymeric dosage form for sustained dehvery raises questions about swallowing or aspirating the device. The surface area is small, and patient comfort should be addressed by designing a small (less than 2 cm ), thin (less than 0.1 mm (4 mil) thick) device that conforms to the mucosal surface. The buccal route may prove useful for peptide or protein dehvery because of the absence of protease activity in the sahva. However, the epithelium is relatively tight, based on its electrophysiological properties. An average conductance in the dog is 1 mS/cm (57) as compared to conductances of about 27 and 10 mS/cm in the small intestine and nasal mucosa, respectively (58,59) these may be classified as leaky epitheha. [Pg.226]

Finer particles ( < 3 pm), termed respirable particles, pass beyond the ex-trathoracic airways and enter the tracheobronchial tree. Impaction plays a significant role near the tracheal jet, but sedimentation predominates as the effects of rapid conduit expansion dampen in the distal trachea and beyond. Sedimentation occurs when gravitational forces exerted on a particle equal drag forces, i.e., when particle velocity falls to u . As mean inspiratory air-stream velocity gradually declines along the tracheobronchial tree, particle momentum diminishes and 0.5-3 pm MMAD particles settle out of the airflow and onto mucosal surfaces. [Pg.224]

Cole, P. (1954). Respiratory mucosal vascular responses, air conditioning and thermoregulation./. Laryngol. Otol. 68, 613-622. [Pg.230]

Paulsson, B., Bende, M., and Ohim, P. (1985). Nasal mucosal blood flow at rest and during exercise. Acta Otolaryngol. (Stockh.) 99, 140-143. [Pg.231]

Proctor, D. F., Andersen, 1 and Lundqvist, G, R. (1977a). human nasal mucosal function at controlled temperatures. Respiration Physiology 30, 109-124. [Pg.231]

FIGURE 10.16 The H+,lO-ATPase of gastric mucosal cells mediates proton transport into the stomach. Potassimn ions are recycled by means of an associated K /Cl cotransport system. The action of these two pnmps results in net transport of and Cl into the stomach. [Pg.307]

Schleim-igkelt, /. sliminess, mucosity. -mem-bran /. mucous membrane, -pilz m. slime fxmgus, sHme mold (Myxomycetea). [Pg.390]


See other pages where Mucositis is mentioned: [Pg.218]    [Pg.18]    [Pg.142]    [Pg.344]    [Pg.312]    [Pg.442]    [Pg.155]    [Pg.171]    [Pg.469]    [Pg.493]    [Pg.495]    [Pg.497]    [Pg.497]    [Pg.498]    [Pg.360]    [Pg.360]    [Pg.439]    [Pg.441]    [Pg.474]    [Pg.496]    [Pg.70]    [Pg.225]    [Pg.211]    [Pg.212]    [Pg.216]    [Pg.217]    [Pg.219]    [Pg.220]    [Pg.230]    [Pg.310]    [Pg.256]    [Pg.284]    [Pg.297]    [Pg.307]    [Pg.603]    [Pg.463]   
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See also in sourсe #XX -- [ Pg.158 ]

See also in sourсe #XX -- [ Pg.403 ]




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Absorption enhancers mucosal application

Absorption mucosal

Accumulation of T Lymphocytes at Mucosal Sites

Adjuvants and the Mucosal Surface

Airway obstruction, mucosal edema

Allergic mucosal inflammation

Antigen , mucosal delivery

Bioavailability mucosal barrier

Bronchial mucosal inflammation

Buccal mucosal cells

Chemotherapy mucositis with

Columnar mucosal cells

Common mucosal immune system

Contribution of Mucosal Edema to Airway Obstruction

Drug application mucosal

Drug delivery mucosal

Drug release mucosal vaccines

Endoscopic mucosal resection

Engineering Lactic Acid Bacteria and Bifidobacteria for Mucosal Delivery of Health Molecules

Enzymes cholesterol esterase, mucosal

Fluorouracil mucositis with

Gastric mucosal barrier

Gastric mucosal barrier damage

Gastric mucosal exfoliant activity

Gastric mucosal protection, drugs

Gastrointestinal mucosal injury

Gastrointestinal tract mucosal immune system

Gastrointestinal tract mucosal metabolism

Histamine mucosal

INDEX mucosal

Immune responses mucosal surfaces

Infections mucosal

Inflammatory bowel disease mucosal damage

Intestinal goblet cells, vitamin A deficiency mucosal cell proliferation

Intestinal mucosal cells

Intestinal mucosal surface

Lesions, mucosal

Luminal mucosal surface

Mast cells mucosal

Mucosa common mucosal

Mucosal

Mucosal

Mucosal addressin cell adhesion

Mucosal addressin cell adhesion molecule-1 (MAdCAM

Mucosal adjuvants

Mucosal administration

Mucosal antibodies

Mucosal barrier

Mucosal barrier agents

Mucosal barrier presence

Mucosal block

Mucosal block theory

Mucosal block, iron absorption

Mucosal cell layer

Mucosal cells

Mucosal cells function

Mucosal damage

Mucosal defense

Mucosal defense, gastrointestinal

Mucosal delivery

Mucosal delivery, controlled-release

Mucosal disinfection

Mucosal epithelial barrier

Mucosal epithelial cells, adhesion

Mucosal epithelium

Mucosal extraction ratio

Mucosal formulations

Mucosal function

Mucosal glands

Mucosal hyperplasia

Mucosal immune system

Mucosal immune system organization

Mucosal immunity

Mucosal immunogenicity

Mucosal inflammation

Mucosal integrity

Mucosal junction

Mucosal lesion, malignant

Mucosal membrane maturation

Mucosal membrane permeability

Mucosal membrane, nasal

Mucosal membranes

Mucosal metabolism

Mucosal oedema

Mucosal permeability, regional differences

Mucosal protection

Mucosal reconstruction

Mucosal route, vaccination

Mucosal routes of delivery

Mucosal surface

Mucosal surface area

Mucosal system

Mucosal targeting molecule

Mucosal tissue irritation

Mucosal tolerance

Mucosal tolerance effects

Mucosal tolerance importance

Mucosal tolerance induction

Mucosal transport process

Mucosal ulceration

Mucosal vaccination

Mucosal vaccination/immunization

Mucosal) Phase

Mucosal-associated lymphoid tissue

Mucosal-associated lymphoid tissue MALT)

Mucosally targeted protein

Mucositis chemotherapy-induced

Mucositis docetaxel

Mucositis methotrexate

Mucositis paclitaxel

Mucositis temsirolimus

Mucositis treatment

Nasal mucosal erythema

Oral mucosal cell sheets

Oral mucosal membranes

Oral mucositis

Oral mucositis, treatment

Oral vaccination mucosal adjuvants

Oral vaccination mucosal immunization

Other Agents Targeting Mucosal Bile Acid Exposure

Parenteral and mucosal vaccination

Polymer-mucosal adhesive properties

Polyp-simulating mucosal prolapse syndrome

Probiotics mucosal cells

Production of Mucosal Damage

Proximal small intestine mucosal surface

Regulatory T Cells by Mucosal Immunization

Respiratory tract, mucosal immune

Respiratory tract, mucosal immune response

Stress related mucosal damage

Stress-related mucosal bleeding

Stress-related mucosal bleeding prevention

Stress-related mucosal damage prophylaxis

Stress-related mucosal damage prophylaxis protocol

Systemic mucosal drug delivery

Toxic responses of skin and mucose membranes

Vaccine mucosal immune response

Vaccines vaginal mucosal

Viruses antigens, mucosal delivery

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