Literature DB >> 6969987

Needs for animal models of human diseases of the respiratory system.

L M Reid.   

Abstract

Animal models are of two types those that occur spontaneously and those that the scientist produces by artefact. One value of spontaneously occurring models is that if pathogenetic mechanisms are identified, they give new leads for the study of human disease. There is a need for spontaneously occurring examples of so-called primary or idiopathic pulmonary fibrosis, pulmonary hypertension (arterial or venous), and emphysema. Acquired or artefactual models of each of these conditions are available and have led to better understanding of the pathological changes, but they have not led to identification of the basic or primary abnormality. A naturally occurring model of cystic fibrosis could be a major event in our control of this disease. A spontaneously occurring form of asthma is needed as a bridge between experiment and patient. Artefactual models that are needed are of bronchopulmonary dysplasia and shock lung. There is probably enough agreement--but only just--on the nature of bronchopulmonary dysplasia for specific needs to be identified. Here the questions concern the choice of an appropriate species--or several--in which to study the premature lung and its adaptation to air breathing and supportive therapy. Knowledge of comparative anatomy and physiology must influence choice of species for certain models. For adult respiratory failure, or shock lung, a model is needed that progresses to pulmonary hypertension. Spontaneous models of interstitial pneumonia and of infection, both viral and bacterial, are needed. An animal model of a disease is only as useful as the questions we ask of it.

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Mesh:

Year:  1980        PMID: 6969987      PMCID: PMC1903625     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  31 in total

Review 1.  Hyaline membrane disease.

Authors:  P M Farrell; M E Avery
Journal:  Am Rev Respir Dis       Date:  1975-05

2.  The pulmonary circulation in cystic fibrosis.

Authors:  D Ryland; L Reid
Journal:  Thorax       Date:  1975-06       Impact factor: 9.139

3.  The physical and chemical properties of bronchial secretion.

Authors:  J Charman; T Lopez-Vidriero; E Keal; L Reid
Journal:  Br J Dis Chest       Date:  1974-10

4.  Distribution of mechanical stress in the lung, a possible factor in localisation of pulmonary disease.

Authors:  J B West
Journal:  Lancet       Date:  1971-04-24       Impact factor: 79.321

5.  The radiographic appearances in primary and in thrombo-embolic pulmonary hypertension.

Authors:  G Anderson; L Reid; G Simon
Journal:  Clin Radiol       Date:  1973-01       Impact factor: 2.350

6.  Arterial changes in Crotalaria spectabilis-induced pulmonary hypertension in rats.

Authors:  A Hislop; L Reid
Journal:  Br J Exp Pathol       Date:  1974-04

7.  Localization of antigen in experimental bronchoconstriction in guinea pigs.

Authors:  J B Richardson; J C Hogg; T Bouchard; D L Hall
Journal:  J Allergy Clin Immunol       Date:  1973-09       Impact factor: 10.793

8.  Primary pulmonary hypertension: a case report including electronmicroscopic study.

Authors:  B Meyrick; S W Clarke; C Symons; D J Woodgate; L Reid
Journal:  Br J Dis Chest       Date:  1974-01

9.  Diffuse pulmonary alveolar fibrosis.

Authors:  J G Scadding
Journal:  Thorax       Date:  1974-05       Impact factor: 9.139

10.  Lack of dynein arms in immotile human spermatozoa.

Authors:  B A Afzelius; R Eliasson; O Johnsen; C Lindholmer
Journal:  J Cell Biol       Date:  1975-08       Impact factor: 10.539

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  1 in total

1.  A new mutation, gld, that produces lymphoproliferation and autoimmunity in C3H/HeJ mice.

Authors:  J B Roths; E D Murphy; E M Eicher
Journal:  J Exp Med       Date:  1984-01-01       Impact factor: 14.307

  1 in total

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