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2.
Circ Res ; 73(4): 649-55, 1993 Oct.
Article in English | MEDLINE | ID: mdl-8396502

ABSTRACT

The role of catecholamines in ischemic preconditioning is unclear. Accordingly, the effects of tyramine-induced norepinephrine release and alpha 1-receptor blockade were examined. Ischemic preconditioning with a 5-minute coronary occlusion 10 minutes before a 30-minute ischemic interval resulted in only 7.7 +/- 3.1% infarction of the risk area, significantly less than that in control rabbits with isolated 30-minute coronary occlusions (34.4 +/- 3.2%, P < .01). Intravenous infusion of tyramine 10 minutes before 30 minutes of ischemia also protected the heart from infarction to an extent similar to that seen with ischemic preconditioning (6.9 +/- 2.4% infarction). This protection observed with tyramine infusion was eliminated by alpha 1-receptor blockade with BE 2254 (36.8 +/- 2.6% infarction) but was unaffected by beta-blockade with propranolol (10.5 +/- 2.4% infarction). Furthermore, the protection was unaffected when the tyramine-induced hypertension was attenuated by allowing blood to flow into a volume reservoir (3.9 +/- 0.8% infarction, P < .01 vs control value). The nonselective adenosine-receptor blocker PD 115,199 also eliminated tyramine-induced protection (40.2 +/- 5.6% infarction), indicating that adenosine is involved in adrenergic-mediated protection. BE 2254 could not block ischemic preconditioning (3.9 +/- 1.1% infarction, P < .01 vs control value). Therefore, catecholamine release before prolonged ischemia can protect the heart from infarction via the alpha 1-receptor, but adenosine receptor stimulation is also involved. alpha-Adrenergic stimulation does not appear to be critical to the protection observed after ischemic preconditioning.


Subject(s)
Catecholamines/physiology , Myocardial Ischemia/physiopathology , Receptors, Purinergic/physiology , Adenosine/physiology , Animals , Female , Male , Rabbits , Rats , Receptors, Adrenergic, alpha/physiology , Species Specificity , Tyramine/pharmacology
3.
Cardiovasc Res ; 27(4): 556-8, 1993 Apr.
Article in English | MEDLINE | ID: mdl-8324785

ABSTRACT

OBJECTIVE: Preconditioning the heart with 5 min of ischaemia followed by reperfusion renders the myocardium resistant to infarction from subsequent ischaemia. This protection lasts for about 1 h. The aim of this study was to test whether the protection could be reinstated with a second episode of preconditioning after protection from an initial episode had worn off. METHODS: To induce infarction animals experienced 30 min of coronary artery occlusion and then 3 h reperfusion. Ischaemic preconditioning was accomplished with 5 min of coronary branch occlusion. In one group of rabbits the subsequent reperfusion period was prolonged to 2 h to permit protection to wear off before the 30 min coronary occlusion was initiated. In another group a second 5 min coronary occlusion was performed at the end of the 2 h reperfusion. After 10 min of reperfusion the 30 min ischaemic period began. Control animals experienced only the 30 min ischaemia and 3 h reperfusion. Infarct volume was measured with tetrazolium and expressed as a percentage of the ischaemic zone volume. RESULTS: Average infarct size in seven control rabbits [36.0 (SEM 2.0)% of the ischaemic zone] was not significantly different from that in eight rabbits with the prolonged coronary occlusion occurring 2 h after the preconditioning stimulus [28.6 (2.9)% infarction]. In contrast infarcts were significantly smaller in the re-preconditioned group of seven rabbits [8.3 (4.2)%] and comparable to those previously seen with a single preconditioning stimulus followed 10 min later by the 30 min occlusion [6.1 (1.8)%]. CONCLUSIONS: The rabbit heart can be protected with a second preconditioning stimulus after protection from an initial period of preconditioning has subsided.


Subject(s)
Myocardial Infarction/prevention & control , Myocardial Ischemia , Myocardial Reperfusion/methods , Animals , Female , Male , Myocardial Infarction/pathology , Myocardial Ischemia/pathology , Myocardium/pathology , Rabbits , Time Factors
4.
Laryngoscope ; 91(2): 260-4, 1981 Feb.
Article in English | MEDLINE | ID: mdl-7464387

ABSTRACT

Bilateral lesions which appeared clinically to be branchial cleft sinuses were removed from a patient's neck. One was indeed a branchial cleft sinus, with elements of salivary tissue, but the other proved to be pure salivary tissue with a duct characteristic of a salivary gland. The embryology and clinical characteristics of heterotopic salivary glands are discussed. The occurrence of a heterotopic gland together with a branchial cleft sinus supports the contention that the heterotopic glands arise through errors of development in the branchial apparatus.


Subject(s)
Branchioma/pathology , Choristoma/pathology , Head and Neck Neoplasms/pathology , Salivary Glands , Child , Humans , Male
5.
Otolaryngol Head Neck Surg ; 89(1): 87-91, 1981.
Article in English | MEDLINE | ID: mdl-6784088

ABSTRACT

An attempt has been made to compare the long-term results using preoperative radiation and surgery with radiation therapy alone in the treatment of squamous cell carcinoma of the pyriform sinus. There is a 33% survival for the combined therapy group and a 6% survival for the curative radiation group. Large primary lesions and the presence of cervical adenopathy portend a grave prognosis. The various surgical procedures used are presented with the extent of the primary lesion as the determining factor.


Subject(s)
Carcinoma, Squamous Cell/therapy , Hypopharynx , Pharyngeal Neoplasms/therapy , Aged , Carcinoma, Squamous Cell/radiotherapy , Carcinoma, Squamous Cell/surgery , Female , Humans , Male , Middle Aged , Neoplasm Staging , Pharyngeal Neoplasms/radiotherapy , Pharyngeal Neoplasms/surgery , Prognosis , Retrospective Studies , Time Factors
6.
Arch Otolaryngol ; 105(8): 449-54, 1979 Aug.
Article in English | MEDLINE | ID: mdl-313781

ABSTRACT

The campomelic syndrome is characterized by dwarfism, craniofacial anomalies, bowing of the tibiae and femora, cutaneous dimpling overlying the tibial bend, respiratory distress, and early death. Otolaryngologic manifestations include flat facies with a broad nasal bridge, low-set ears, cleft palate, mandibular hypoplasia, and tracheobronchial malacia. The underlying pathologic feature appears to be disturbance in cartilage growth involving the affected bones and the respiratory tract cartilage. The cause is unknown. We report clinical and histopathologic features in two cases of this syndrome. The endochondral layer of the otic capsule contained no cartilage cells. The cochlea was short and flattened, presenting a scala communis. The vestibule and the canals were deformed by bone invasion. Defective endochondral ossification of the petrooccipital synchondroses possibly explains the shortened skull base seen in this syndrome. The tracheobronchial malacia significantly contributes to respiratory distress and neonatal death.


Subject(s)
Craniofacial Dysostosis/complications , Dwarfism/complications , Temporal Bone/pathology , Abnormalities, Multiple , Bone Diseases/diagnostic imaging , Bone Diseases/pathology , Cochlea/pathology , Craniofacial Dysostosis/diagnostic imaging , Dwarfism/diagnostic imaging , Ear, External/pathology , Ear, Inner/pathology , Ear, Middle/pathology , Female , Humans , Infant, Newborn , Male , Radiography , Vestibule, Labyrinth/pathology
10.
Ann Otol Rhinol Laryngol ; 87(3 Pt 1): 399-403, 1978.
Article in English | MEDLINE | ID: mdl-655581

ABSTRACT

The temporal bone findings in a case of hemifacial microsomia are described with photographs. The right facial hypoplasia was associated with anophthalmia and microtia on the same side. The right petrous bone was hypoplastic and showed total superior dehiscence of the internal acoustic meatus. Th otic capsule was deformed with an underdeveloped cochlear modiolus grossly deficient in spiral ganglion population. The spiralling cochlear shell showed partial deficiency of the interscalar septum between the middle and apical coils. The cochlear duct was shorter than that on the normal side; the organ of Corti however was normal. The vestibular system did not show any structural abnormality except for the degeneration and reduction of the Scarpa's ganglion cells and nerve fibers. An additional interesting fact was that the facial nerve was totally absent in the temporal bone except for its nervus intermedius component.


Subject(s)
Abnormalities, Multiple/pathology , Ear, Inner/pathology , Ear/abnormalities , Temporal Bone/pathology , Anophthalmos/pathology , Child, Preschool , Face/abnormalities , Facial Nerve/pathology , Functional Laterality , Humans , Infant , Petrous Bone/pathology , Syndrome
11.
Ann Otol Rhinol Laryngol Suppl ; 87(1 Pt 3 Suppl 46): 1-12, 1978.
Article in English | MEDLINE | ID: mdl-414649

ABSTRACT

Familial dysautonomia, or Riley-Day syndrome, is inherited in an autosomal recessive fashion and occurs almost exclusively in Jewish families. This disorder is characterized by a smooth tongue devoid of fungiform papillae and of taste buds, and is clinically associated with poor taste discrimination. An unsteady gait and dizziness on change in position are also common presenting symptoms. This study reports the histopathological findings of eight temporal bones from four patients with documented familial dysautonomia. For the control series, 13 normal temporal bones were also studied. The most striking finding in the dysautonomic patients was an extreme paucity of geniculate ganglion cells (P less than 0.001). A statistically significant reduction in the number of neurons was also found both in the superior and in the inferior divisions of the vestibular nerve (P less than 0.001). The paucity of the geniculate ganglion cells correlates well with the impairment of the taste in dysautonomic individuals, since the afferent fibers leaving taste buds of the anterior two-thirds of the tongue run via the chorda tympani and have their cell bodies in the geniculate ganglion. Furthermore, the reduction in the number of Scarpa's ganglion cells observed in the dysautonomic patients studied here could account for a poor response to caloric test, positional vertigo and an unsteady gait in this condition.


Subject(s)
Dysautonomia, Familial/pathology , Temporal Bone/pathology , Adolescent , Adult , Age Factors , Auditory Pathways/pathology , Cell Count , Child , Child, Preschool , Dysautonomia, Familial/physiopathology , Facial Nerve/pathology , Female , Geniculate Ganglion/pathology , Humans , Infant , Lacrimal Apparatus/physiopathology , Male , Middle Aged , Respiration Disorders/physiopathology , Tongue/pathology , Vestibular Nerve/pathology , Vestibule, Labyrinth/physiopathology , Vestibulocochlear Nerve/pathology
13.
JAMA ; 234(2): 171-3, 1975 Oct 13.
Article in English | MEDLINE | ID: mdl-240948

ABSTRACT

Cephalexin monohydrate suspension was used in the treatment of 97 children with otitis media. Pretreatment middle-ear exudate specimens in pure or mixed culture yielded Diplococcus pneumoniae in 47 cases, Haemophilus influenzae in 26, Neisseria catarrhalis in 20, group A beta-hemolytic streptococci in 13, and Staphylococcus aureus in one. The usual dosage was 100 mg/kg/day given orally in divided doses for 10 to 12 days. After 48 hours of treatment, follow-up cultures showed that therapy had been successful in 90 children; 81 remained clinically and bacteriologically free of disease for at least three weeks following therapy. Of the seven children for whom therapy failed, H influenzae persisted in five and D pneumoniae in two. Acceptance of the drug was entirely satisfactory with no important side effects encountered.


Subject(s)
Cephalexin/therapeutic use , Otitis Media/drug therapy , Adolescent , Age Factors , Cephalexin/administration & dosage , Child , Child, Preschool , Drug Tolerance , Ear, Middle/metabolism , Exudates and Transudates/microbiology , Haemophilus influenzae/isolation & purification , Humans , Infant , Neisseria/isolation & purification , Otitis Media/microbiology , Staphylococcus aureus/isolation & purification , Streptococcus pneumoniae/isolation & purification , Streptococcus pyogenes/isolation & purification , Suspensions
14.
Laryngoscope ; 85(8): 1290-7, 1975 Aug.
Article in English | MEDLINE | ID: mdl-1160460

ABSTRACT

Laryngofissure and cordectomy is one of the first of the successful surgical procedures for the cure of cancer limited to the vocal cord. When the lesion is confined to the membranous cord and the motion of the cord is not impaired, cure rates ranging from 85 to 98 percent have been reported. Decline in the use of the procedure is due to the success of radiation therapy in achieving comparable cure rates while preserving normal voice quality. Hemilaryngectomy procedures are now done where laryngofissure and cordectomy had previously been indicated. The more extensive procedure gives greater security due to wider margins of resection and increase applicability, particularly when the lesion involves the anterior commissure. Although the indications for laryngofissure have diminished, the surgeon may use it when a simple, less extensive procedure is called for.


Subject(s)
Larynx/surgery , Vocal Cords/surgery , Anesthesia, General , Humans , Laryngeal Neoplasms/mortality , Laryngeal Neoplasms/radiotherapy , Laryngeal Neoplasms/surgery , Laryngectomy , Methods , Neoplasm Recurrence, Local
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