19 research outputs found
Influence of tricalcium silicate on course of traumatic pulpitis
The use of Tricalcium Silicate (TS) as an odontotropic preparation makes it possible to create a hermetic crown restoration with a high degree of adhesion. However, the use of TS silicate by direct pulp capping remains disputable. The aim of this study was to determine the effects of TS on course of traumatic pulpitis by detection of morpho-functional peculiarities of changes in pulp tissue. We performed experimental investigation (on rabbits, males, aging three-month) for study of the morphofunctional changes of the pulp tissues with modeling of traumatic pulpitis and direct pulp capping with TS preparation (8 animals, investigated group) and calcium hydroxide (Calasept, NORDISKA DENTAL) preparation (8 animals, comparison group). After 2nd and 6th weeks tissues of tooth were fixed in 10% formalin with performing routine proceeding after decalcification and making histological slides which were investigated. Manifestations of protective adaptive mechanisms have been revealed in the form of inflammatory process two weeks after the injury in the pulp tissue with its resolution six weeks after performing of direct pulp capping with TS with replacement of necrotic area by connective tissue with their delimitation from viable pulp tissue against a background of intensive formation of capillaries. Morphometric study proved dynamical changes of vascular number cross-sections per 1 mm2 from 69.31Β±4.76 (2 weeks) to 47.38Β±4.12 (6 weeks) with 49.2Β±3.47 vascular density in intact group. Cellular density of odontoblasts as changed from 3.92Β±1.03 x103 per 1 mm2 (2 weeks) to 7.49Β±1.51 x103 per 1 mm2 (6 weeks) with 8.3Β±1.02 x103 per 1 mm2 cellular density in intact group. Thus it can be argued that the use of TS as a material for direct pulp capping promotes more active regeneration processes.
Π¦Π΅Π»ΡΡ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΡ ΡΠ²ΠΈΠ»ΠΎΡΡ ΠΎΠΏΡΠ΅Π΄Π΅Π»Π΅Π½ΠΈΠ΅ Π²Π»ΠΈΡΠ½ΠΈΡ ΡΡΠΈΠΊΠ°Π»ΡΡΠΈΠΉΡΠΈΠ»ΠΈΠΊΠ°ΡΠ° Π½Π° ΡΠ΅ΡΠ΅Π½ΠΈΠ΅ ΡΡΠ°Π²ΠΌΠ°ΡΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ ΠΏΡΠ»ΡΠΏΠΈΡΠ°. ΠΠΎΡΡΠ°Π²Π»Π΅Π½ ΡΠΊΡΠΏΠ΅ΡΠΈΠΌΠ΅Π½Ρ Π½Π° 3-ΠΌΠ΅ΡΡΡΠ½ΡΡ
ΠΊΡΠΎΠ»ΠΈΠΊΠ°Ρ
ΡΠ°ΠΌΡΠ°Ρ
Π΄Π»Ρ ΠΈΠ·ΡΡΠ΅Π½ΠΈΡ ΠΌΠΎΡΡΠΎΡΡΠ½ΠΊΡΠΈΠΎΠ½Π°Π»ΡΠ½ΡΡ
ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΠΉ ΡΠΊΠ°Π½ΠΈ ΠΏΡΠ»ΡΠΏΡ Ρ ΠΌΠΎΠ΄Π΅Π»ΠΈΡΠΎΠ²Π°Π½ΠΈΠ΅ΠΌ ΡΡΠ°Π²ΠΌΠ°ΡΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ ΠΏΡΠ»ΡΠΏΠΈΡΠ° ΠΈ ΠΏΡΡΠΌΡΠΌ ΠΏΠΎΠΊΡΡΡΠΈΠ΅ΠΌ ΠΏΡΠ»ΡΠΏΡ ΡΡΠΈΠΊΠ°Π»ΡΡΠΈΠΉΡΠΈΠ»ΠΈΠΊΠ°ΡΠΎΠΌ (8 ΠΆΠΈΠ²ΠΎΡΠ½ΡΡ
, ΠΈΡΡΠ»Π΅Π΄ΡΠ΅ΠΌΠ°Ρ Π³ΡΡΠΏΠΏΠ°) ΠΈ Π³ΠΈΠ΄ΡΠΎΠΊΡΠΈΠ΄ΠΎΠΌ ΠΊΠ°Π»ΡΡΠΈΡ (Calasept, NORDISKA DENTAL) (8 ΠΆΠΈΠ²ΠΎΡΠ½ΡΡ
, Π³ΡΡΠΏΠΏΠ° ΡΡΠ°Π²Π½Π΅Π½ΠΈΡ). Π‘ΠΏΡΡΡΡ 2 ΠΈ 6 Π½Π΅Π΄Π΅Π»ΠΈ ΡΠΊΠ°Π½ΠΈ Π·ΡΠ±Π° ΡΠΈΠΊΡΠΈΡΠΎΠ²Π°Π»ΠΈ Π² 10% ΡΠΎΡΠΌΠ°Π»ΠΈΠ½Π΅ ΠΈ ΠΏΠΎΡΠ»Π΅ Π΄Π΅ΠΊΠ°Π»ΡΡΠΈΡΠΈΠΊΠ°ΡΠΈΠΈ ΠΈ ΡΡΡΠΈΠ½Π½ΠΎΠΉ ΠΏΡΠΎΠ²ΠΎΠ΄ΠΊΠΈ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π»ΠΈ Π³ΠΈΡΡΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠΈΠ΅ ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΡ. Π‘ΠΏΡΡΡΡ 2 Π½Π΅Π΄Π΅Π»ΠΈ ΠΏΠΎΡΠ»Π΅ Π½Π°Π½Π΅ΡΠ΅Π½ΠΈΡ ΡΡΠ°Π²ΠΌΡ Π² ΡΠΊΠ°Π½ΠΈ ΠΏΡΠ»ΡΠΏΡ ΠΎΠ±Π½Π°ΡΡΠΆΠ΅Π½Ρ ΠΏΡΠΎΡΠ²Π»Π΅Π½ΠΈΡ Π·Π°ΡΠΈΡΠ½ΠΎ-ΠΏΡΠΈΡΠΏΠΎΡΠΎΠ±ΠΈΡΠ΅Π»ΡΠ½ΡΡ
ΠΌΠ΅Ρ
Π°Π½ΠΈΠ·ΠΌΠΎΠ² Π² Π²ΠΈΠ΄Π΅ Π²ΠΎΡΠΏΠ°Π»ΠΈΡΠ΅Π»ΡΠ½ΠΎΠ³ΠΎ ΠΏΡΠΎΡΠ΅ΡΡΠ° Ρ Π΅Π³ΠΎ ΡΠ°Π·ΡΠ΅ΡΠ΅Π½ΠΈΠ΅ΠΌ, ΠΏΡΠΈ ΠΊΠΎΡΠΎΡΠΎΠΌ Π½Π°Π±Π»ΡΠ΄Π°Π΅ΡΡΡ Π·Π°ΠΌΠ΅ΡΠ΅Π½ΠΈΠ΅ Π·ΠΎΠ½Ρ Π½Π΅ΠΊΡΠΎΠ·Π° ΡΠΎΠ΅Π΄ΠΈΠ½ΠΈΡΠ΅Π»ΡΠ½ΠΎΠΉ ΡΠΊΠ°Π½ΡΡ Π½Π° ΡΠΎΠ½Π΅ ΠΈΠ½ΡΠ΅Π½ΡΠΈΠ²Π½ΠΎΠ³ΠΎ Π½ΠΎΠ²ΠΎΠΎΠ±ΡΠ°Π·ΠΎΠ²Π°Π½ΠΈΡ ΠΊΠ°ΠΏΠΈΠ»Π»ΡΡΠΎΠ², ΡΡΠΎ Ρ
Π°ΡΠ°ΠΊΡΠ΅ΡΠΈΠ·ΡΠ΅ΡΡΡ ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΠ΅ΠΌ ΠΏΠ»ΠΎΡΠ½ΠΎΡΡΠΈ ΡΠΎΡΡΠ΄ΠΎΠ² ΠΌΠΈΠΊΡΠΎΡΠΈΡΠΊΡΠ»ΡΡΠΎΡΠ½ΠΎΠ³ΠΎ ΡΡΡΠ»Π°. ΠΠΎΡΡΠΎΠΌΠ΅ΡΡΠΈΡΠ΅ΡΠΊΠΎΠ΅ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΠ΅ ΠΏΠΎΠΊΠ°Π·Π°Π»ΠΎ Π΄ΠΈΠ½Π°ΠΌΠΈΡΠ΅ΡΠΊΠΈΠ΅ ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΡ ΠΊΠΎΠ»ΠΈΡΠ΅ΡΡΠ²Π° ΡΠΎΡΡΠ΄ΠΈΡΡΡΡ
ΡΠ΅ΡΠ΅Π½ΠΈΠΉ Ρ 69,31Β±4,76/ΠΌΠΌ2 (2 Π½Π΅Π΄Π΅Π»ΠΈ) Π΄ΠΎ 47,38Β±4,12/ΠΌΠΌ2 (6 Π½Π΅Π΄Π΅Π»Ρ) ΠΏΡΠΈ 49,2Β±3,47/ΠΌΠΌ2 Π² ΠΈΠ½ΡΠ°ΠΊΡΠ½ΠΎΠΉ Π³ΡΡΠΏΠΏΠ΅. ΠΠ»ΠΎΡΠ½ΠΎΡΡΡ ΠΎΠ΄ΠΎΠ½ΡΠΎΠ±Π»Π°ΡΡΠΎΠ² ΠΈΠ·ΠΌΠ΅Π½ΠΈΠ»Π°ΡΡ
Ρ 3,92Β±1,03Γ103/ΠΌΠΌ2 (2 Π½Π΅Π΄Π΅Π»ΠΈ) Π΄ΠΎ 7,49Β±1,51Γ103/ΠΌΠΌ2 (6 Π½Π΅Π΄Π΅Π»Ρ) ΠΏΡΠΈ 8,3Β±1,02Γ103/ΠΌΠΌ2 ΠΊΠ»Π΅ΡΠΎΡΠ½ΠΎΠΉ ΠΏΠ»ΠΎΡΠ½ΠΎΡΡΠΈ Π² ΠΈΠ½ΡΠ°ΠΊΡΠ½ΠΎΠΉ Π³ΡΡΠΏΠΏΠ΅. Π’Π°ΠΊΠΈΠΌ ΠΎΠ±ΡΠ°Π·ΠΎΠΌ, ΡΠ»Π΅Π΄ΡΠ΅Ρ ΠΏΡΠ΅Π΄ΠΏΠΎΠ»ΠΎΠΆΠΈΡΡ, ΡΡΠΎ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΠ΅ ΡΡΠΈΠΊΠ°Π»ΡΡΠΈΠΉΡΠΈΠ»ΠΈΠΊΠ°ΡΠ° Π² ΠΊΠ°ΡΠ΅ΡΡΠ²Π΅ ΠΌΠ°ΡΠ΅ΡΠΈΠ°Π»Π° Π΄Π»Ρ ΠΏΡΡΠΌΠΎΠ³ΠΎ ΠΏΠΎΠΊΡΡΡΠΈΡ ΠΏΡΠ»ΡΠΏΡ ΡΠΏΠΎΡΠΎΠ±ΡΡΠ²ΡΠ΅Ρ Π±ΠΎΠ»Π΅Π΅ Π°ΠΊΡΠΈΠ²Π½ΡΠΌ ΠΏΡΠΎΡΠ΅ΡΡΠ°ΠΌ ΡΠ΅Π³Π΅Π½Π΅ΡΠ°ΡΠΈΠΈ
Implementation and analysis of Babesia immunoassay testing
Lifelong withdrawal from the donor population of those who have been diagnosed with babesiosis must be used for transmission prevention. The aim of the study was a detection of Babesia antibodies level with the usage of experimental Babesia divergens whole-cell slide antigen and commercial B. microti immunofluorescence assay substrate slide (Fuller Laboratories, USA). Methods. Experimental B. divergens whole-cell slide antigen in addition to commercial B. microti IFA substrate slide was used to create a diagnostic kit for serum Babesia antibodies level detecting, as well as for a babesiosis serodiagnosis clinical trial of different origins blood samples (patients with Lyme disease, rheumatoid arthritis and toxoplasmosis; human blood donors; cattle).
Results. Antibodies to B. divergens (5.4%) and B. microti (2.3%) were detected with higher (p <0.05) frequency at Lyme disease patients (16.7%) than at blood donors (1.7%). Diagnostically significant IgG titres (= 1:128) were found in 13.3% of blood samples from Lyme disease patients and 1.7% from blood donors. Specific IgM were also found in 13.3% blood samples from Lyme disease patients. Among blood samples from Lyme disease patients, in which diagnostically significant titres of Babesia antibodies were detected (16.7%), 60% of them were represented by IgG and IgM (rA= 0.63), and in 40% only
one of them reached diagnostically significant titre. Conclusions. Advantages of babesiosis IFA diagnostics are combined with its significant disadvantages (principle of evaluation, low sensitivity in the initial period of the disease, probability of false positives, absence of validated test systems and research protocols for B. divergens and B. divergens-like species)
Anaplasmosis: experimental immunodeficient state mod
The recently described anaplasmosis infection is widespread but concerns to the insufficiently known group of diseases. The aim of our research is the development of uniform biological model for reproducing of artificial immunodeficient state by experimental anaplasmosis. Materials and methods: Algorithm of experimental anaplasmosis reproducing, consisted of such consecutive stages: 1) artificial forming of the immunodeficient state at nonlinear white mise (Mus musculus L.); 2) preparation of the tested biological material samples; 3) inoculation by prepared samples of the laboratory animals with the artificially formed immunodeficient state; 4) sampling from the dead or slaughtered (by the method of chloroformed anesthesia) experimental animals of sectional material (organs and targets tissues); 5) verification of aetiology by express detection of causative agents by the method of PCR in the selected samples of sectional material. Results: Biological model of experimental anaplasmosis have been created suitable for realization of both diagnostic and epidemiological, epizootic, ecobiological and other researches of different origin biological material samples, including samples of solid and liquid consistency material. Formed model realised in premature death of experimental animals in 17.4 % cases; resulted in an onset of disease clinical signs without death during the term of supervision in 43.8 % cases; coursed in the absence of the expressed symptoms of infection in 31.3 % cases. Conclusions: Developed biological model of experimental anaplasmosis consists in that as laboratory animals with the increased sensitiveness to the infection and accumulation of causative agent are used white nonlinear mice with the artificially formed immunodeficient state
Cytological transformation of the cervix in immunodeficiency aggravated by alcoholism
Comorbid pathology, high mortality and disability remain an urgent problem for people with the development of an immunodeficiency state, including women of reproductive age
Seroprevalence of babesiosis in immunocompetent and immunocompromised individuals
Interest in Babesia species is gaining an increasing attention as an
emerging tick-borne pathogen. Infection is primarily transmitted through
Ixodes ticks, and alternatively by blood transfusions from asymptomatic
donors.
The aim of the study was detection of Babesia seroprevalence in
different groups of population with the usage of experimental B. divergens
whole-cell slide antigen and commercial B. microti immunofluorescence
assay substrate slide.
Materials and methods. Indirect immunofluorescence assay trial was
performed by testing of 145 blood samples of different origins: healthy
individuals (60 β blood donors), risk groups (30 β HIV-infected
individuals, 30 β Lyme disease patients) and false-positive IFA controls
(10 β seropositive rheumatoid arthritis patients, 15 β patients with
toxoplasmosis).
Results. The study revealed Babesia antibodies to B. divergens (6.9%)
and B. microti (3.4%) that were detected with higher (p <0.05) frequency
in HIV-infected individuals (26.7%) and in Lyme disease patients
(16.7%) than at blood donors (1.7%). Diagnostically significant IgG
titres were detected at 23.3% HIV-infected individuals, 13.3% Lyme
disease patients and by 1.7% of blood donors and patients with
seropositive latent toxoplasmosis. Specific IgM were detected at 20.0%
HIV-infected individuals and 13.3% Lyme disease patients. 57.1% of
diagnostically significant titres in HIV-infected and Lyme disease
patients were represented by IgG and IgM.
Conclusion. Immunofluorescence assay has a limited use in
babesiosis: in acute form with negative microscopy or PCR; in chronic,
asymptomatic and subclinical form with low level of parasitemia; and
in retrospective and epidemiological studies of the population immune
structure. Clinicians need to have increased awareness of babesiosis,
and further studies are needed to clarify the optimal management of
this infection in risk groups (including HIV-infected patients and blood
donors)
The influence of immunodeficiency on the level of CD34-positive cells in the cervix
There are many studies on changes in cervix,
however, there are no data about property of cervical tissue to keep
potential for regeneration under influence of immunodeficiency,
which is very important since it allows escaping severe
irreversible changes in tissue. CD34 stem cells are one of
significant indicator for property of tissual regeneration. So, the
purpose of our study was to identify amount of CD34 stem cells
in the cervix under influence of immunodeficiency of infectious
and non-infectious origin.
Materials and methods. Sectional material of reproductive
women was studied. All subjects were divided into 3 groups:
women who were diagnosed with HIV infection; women
who have identified anamnestic and postmortem signs of
alcohol abuse; group of comparison. After routine testing and
immunohistochemical (IHC) staining to CD34, morphometric
measure was performed. We evaluate presence activities of
stromal cells for detection of connection and relationship
between expression of CD34 and the thickness of the cervical
epithelium, relative volumes of condyloma, cervical dysplasia
severity, degree of infiltration of the mucosal lamina propria
by immunocompetent cells. The obtained digital data were
statistically processed.
Results. Morphological investigation revealed changes of
thickness of the cervical stratified squamous nonkeratinized
epithelium up to 714.23Β±59.21 x 10-6 m in group of HIVinfected women. Relative volumes of condylomas were increased in both investigated groups with presence of pointed,
flat and inverted types. Both low- and high-grade squamous
intraepithelial lesions were detected more often in investigated
goups. Assessment of the degree of infiltration of the mucosal
lamina propria by immunocompetent cells was changed
unevenly with reducing in HIV-group and increasing in alcohol
group. Results of ICH reaction CD34 realized in cytoplasmic
staining with membranous accentuation in all cases of control
group with strong, but reduced level in investigated groups.
Most close connection was observed for cervical dysplasia
severity and CD34 expression.
Conclusions.HIV infection and alcohol abuse have pronounced
pathological effects with cervical changes. The expression of
CD34 is present in 96% of women with immunodeficiency
mainly with strong reaction. It is statistically likely that it does
not depend on such morphological indicators as thickness of the
cervical epithelium, relative volumes of condyloma, degree of
infiltration of the mucosal lamina propria by immunocompetent
cells. The expression of CD34 has statistically close negative
connection with cervical dysplasia severity (r=-0,81) and can be
used for detection of early potential of tissual transformation in
women with immunodeficiency