The review presents the latest literature describing the Central nucleus of the Amygdala complex of the brain (CE), which is an important link in the Central autonomic nervous network. It appears in the early stages of the evolution of the telencephalon. This determines its solid phylogenetic age and explains the heteromorphy, which is manifested by the presence of a number of subnucleus: medial, intermediate, lateral and latero-capsular. The article provides information about the features of cytoarchitectonics, neural organization of subnucleus and neuropeptides. Among the latter, special attention is paid to vasopressin and oxytocin in connection with the identified new way of innervation of the amygdala complex, which has at least two origins: 1. arising from a small population of neurons localized in the intra-amygdalar portion of the bed nucleus of the stria terminalis, and 2.originating from hypothalamic neurosecretory nuclei. Afferent and efferent connections of CE are characterized. A large number of studies define the medial subnucleus as the center of integration of incoming information to the CE and the main channel for its exit from CE. At the same time, the main point where efferent connections of CE follow is the centers of the brain stem that control cardiovascular, respiratory, metabolic and motor functions. Information is provided about the main functions, including the regulation of various forms of social behavior, eating behavior, and involvement in functional reinforcement systems. The results of genetic studies indicate that CE is a derivative of the striatal division of the lateral ganglionic eminence, in the formation of which the expression of the Dlx5 and Lmo4 genes.
本文综述了近年来有关大脑杏仁核复合体中央核(Central nucleus of Amygdala complex of brain, CE)的研究进展，它是中枢自主神经网络中的一个重要环节。它出现在端脑进化的早期阶段。这决定了它的系统发育年龄，并解释了异型性，这种异型性表现为许多亚核的存在:内侧、中间、外侧和后囊。本文介绍了细胞结构、亚核神经组织和神经肽的特点。其中，抗利尿激素和催产素与杏仁核复合体神经支配的新方式有关，其至少有两个起源:1。1 .起源于终末纹床核杏仁核内的一小群神经元;起源于下丘脑的神经分泌核。表征了CE的传入和传出连接。大量研究将内侧亚核定义为输入信息整合到CE的中心，以及信息从CE输出的主要通道。同时，CE的传出连接主要遵循控制心血管、呼吸、代谢和运动功能的脑干中枢。提供了关于主要功能的信息，包括调节各种形式的社会行为、饮食行为和参与功能强化系统。遗传学研究结果表明，CE是侧神经节隆起纹状体分裂的衍生物，其形成过程中表达了Dlx5和Lmo4基因。
{"title":"Structure, function and genoarchitectonics of the Central nucleus of the Brain’s Amygdala","authors":"A. Akhmadeev","doi":"10.17816/morph.110830","DOIUrl":"https://doi.org/10.17816/morph.110830","url":null,"abstract":"The review presents the latest literature describing the Central nucleus of the Amygdala complex of the brain (CE), which is an important link in the Central autonomic nervous network. It appears in the early stages of the evolution of the telencephalon. This determines its solid phylogenetic age and explains the heteromorphy, which is manifested by the presence of a number of subnucleus: medial, intermediate, lateral and latero-capsular. The article provides information about the features of cytoarchitectonics, neural organization of subnucleus and neuropeptides. Among the latter, special attention is paid to vasopressin and oxytocin in connection with the identified new way of innervation of the amygdala complex, which has at least two origins: 1. arising from a small population of neurons localized in the intra-amygdalar portion of the bed nucleus of the stria terminalis, and 2.originating from hypothalamic neurosecretory nuclei. Afferent and efferent connections of CE are characterized. A large number of studies define the medial subnucleus as the center of integration of incoming information to the CE and the main channel for its exit from CE. At the same time, the main point where efferent connections of CE follow is the centers of the brain stem that control cardiovascular, respiratory, metabolic and motor functions. Information is provided about the main functions, including the regulation of various forms of social behavior, eating behavior, and involvement in functional reinforcement systems. The results of genetic studies indicate that CE is a derivative of the striatal division of the lateral ganglionic eminence, in the formation of which the expression of the Dlx5 and Lmo4 genes.","PeriodicalId":74228,"journal":{"name":"Morphology (Dordrecht, Netherlands)","volume":"57 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85844998","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The aim of the study was to identify the localization, percentage and morphometric characteristics of neuronal NO synthase (nNOS)-immunoreactive (IR) neurons in the intramural ganglia of the myenteric (MP) and submucous plexus (SP) of the large intestine of rats of different age groups. Material and methods. The work was performed on Wistar rats aged 1, 10, 20, 30, 60 days and 2 years using immunohistochemical methods. Results. nNOS-IR neurons were found in the large intestine from the moment of birth and during the remaining age periods. In the intramural ganglia of the MP, the largest percentage of nNOS-IR neurons was detected in the newborn rat and decreased in ontogenesis up to 60 days of life, then did not change until senescence. In the SP, nNOS-IR neurons were also detected in the greatest number in newborns, in the next 20 days the percentage decreased significantly, nNOS-IR neurons were not detected in 30-day and two-month-old animals, but again appeared in large numbers in aged rats. The average cross-sectional area of nNOS-IR neurons increased in the MP from birth during the first two months of life. In the SP, the average size of nNOS-IR cells increased in the first 30 days of life and was significantly larger in aged rats compared with other ages. Conclusions. In early postnatal ontogenesis, there is a decrease in the expression of nNOS in neurons of the large intestine and a subsequent increase in aged rats.
{"title":"Age-related changes of neurons from the large intestine containing neuronal nitric oxide synthase","authors":"P. Masliukov, Дарья Аряева, Антонина Будник","doi":"10.17816/morph.110832","DOIUrl":"https://doi.org/10.17816/morph.110832","url":null,"abstract":"The aim of the study was to identify the localization, percentage and morphometric characteristics of neuronal NO synthase (nNOS)-immunoreactive (IR) neurons in the intramural ganglia of the myenteric (MP) and submucous plexus (SP) of the large intestine of rats of different age groups. \u0000Material and methods. The work was performed on Wistar rats aged 1, 10, 20, 30, 60 days and 2 years using immunohistochemical methods. \u0000Results. nNOS-IR neurons were found in the large intestine from the moment of birth and during the remaining age periods. In the intramural ganglia of the MP, the largest percentage of nNOS-IR neurons was detected in the newborn rat and decreased in ontogenesis up to 60 days of life, then did not change until senescence. In the SP, nNOS-IR neurons were also detected in the greatest number in newborns, in the next 20 days the percentage decreased significantly, nNOS-IR neurons were not detected in 30-day and two-month-old animals, but again appeared in large numbers in aged rats. The average cross-sectional area of nNOS-IR neurons increased in the MP from birth during the first two months of life. In the SP, the average size of nNOS-IR cells increased in the first 30 days of life and was significantly larger in aged rats compared with other ages. \u0000Conclusions. In early postnatal ontogenesis, there is a decrease in the expression of nNOS in neurons of the large intestine and a subsequent increase in aged rats.","PeriodicalId":74228,"journal":{"name":"Morphology (Dordrecht, Netherlands)","volume":"239 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76893670","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background. Literature data on the effect of methionine on functional activity and, especially, on morphological changes in the thyroid gland are sporadic. This may be due to a number of reasons, such as: different ages of experimental animals; different dosage of methionine; different seasonality and duration of experiments. Aims: To investigate the morphological changes in the thyroid gland of rats of different ages after methionine administration. Material and methods. The experiments were performed on 48 Wistar male rats of 3 and 15 months of age. Experimental animals received methionine daily for 21 days at a dose of 250 mg / kg of body weight in addition to the standard diet. Histological preparations were made from the thyroid tissue according to the standard method. The gland morphometry was performed on digital images using the computer program Image J. Results. It was found that 21-day administration of methionine to rats of both 3 and 15 months of age led to a decrease in the cross-sectional area of the follicles and colloid, the accumulation index of colloid and the relative area of the conective tissue in the thyroid gland. But the follicular-colloid index, the number of resorption vacuoles in the colloid, and the number of interfollicular islets were increased. Morphological changes in the thyroid gland of 15-month-old experimental rats were manifested to a greater extent than in young animals. Conclusions. Thus, the influence of methionine increases the histomorphological signs of the synthetic activity of the thyroid gland in rats of different ages.
{"title":"Morphological changes in the thyroid gland of rats of different age after administration of methionine","authors":"R. Yanko, М Левашов","doi":"10.17816/morph.110838","DOIUrl":"https://doi.org/10.17816/morph.110838","url":null,"abstract":"Background. Literature data on the effect of methionine on functional activity and, especially, on morphological changes in the thyroid gland are sporadic. This may be due to a number of reasons, such as: different ages of experimental animals; different dosage of methionine; different seasonality and duration of experiments. \u0000Aims: To investigate the morphological changes in the thyroid gland of rats of different ages after methionine administration. \u0000Material and methods. The experiments were performed on 48 Wistar male rats of 3 and 15 months of age. Experimental animals received methionine daily for 21 days at a dose of 250 mg / kg of body weight in addition to the standard diet. Histological preparations were made from the thyroid tissue according to the standard method. The gland morphometry was performed on digital images using the computer program Image J. \u0000Results. It was found that 21-day administration of methionine to rats of both 3 and 15 months of age led to a decrease in the cross-sectional area of the follicles and colloid, the accumulation index of colloid and the relative area of the conective tissue in the thyroid gland. But the follicular-colloid index, the number of resorption vacuoles in the colloid, and the number of interfollicular islets were increased. Morphological changes in the thyroid gland of 15-month-old experimental rats were manifested to a greater extent than in young animals. \u0000Conclusions. Thus, the influence of methionine increases the histomorphological signs of the synthetic activity of the thyroid gland in rats of different ages.","PeriodicalId":74228,"journal":{"name":"Morphology (Dordrecht, Netherlands)","volume":"28 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84284945","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose the study of the ultrastructure of the cerebral cortex of rats in normal and experimental poisoning with dioxin. Materials and methods. We studied the ultrastructure of the cells of the pyramidal layer of the cerebral cortex of rats of the control and experimental groups that were chronic poisoned with small doses of dioxin (2,3,7,8-tetrachlorodibenzo-para-dioxin or TCDD). Morphometric analysis was carried out to determine the length of synaptic clefts, the number of synapses per unit area, the thickness of the myelin layer of the processes and the number of wrappers of myelin sheaths. Results. The pathology of neurons has been observed both at the optical and ultrastructural levels. It is characterized by a decrease in nuclei, cell death, thinning of myelin sheaths and demyelination. The dose of poisoning correlates with the degree of destruction of neurons: with an increase in the dose of dioxin, changes become more significant. The number of synaptic contacts decreases but there is a significant increase in their average length. Conclusions. The processes of demyelination, impaired cellular respiration and destruction of synaptic contacts indicate the ability of dioxin to indirectly cause accelerated aging of neurons and their death (apoptosis).
{"title":"Ultrastructure of rat cerebral cortex cells in normal and experimental dioxin poisoning","authors":"M. Salnikova, V. Саитов, А. Яковлева, А. Голубев","doi":"10.17816/morph.110834","DOIUrl":"https://doi.org/10.17816/morph.110834","url":null,"abstract":"Purpose the study of the ultrastructure of the cerebral cortex of rats in normal and experimental poisoning with dioxin. \u0000Materials and methods. We studied the ultrastructure of the cells of the pyramidal layer of the cerebral cortex of rats of the control and experimental groups that were chronic poisoned with small doses of dioxin (2,3,7,8-tetrachlorodibenzo-para-dioxin or TCDD). Morphometric analysis was carried out to determine the length of synaptic clefts, the number of synapses per unit area, the thickness of the myelin layer of the processes and the number of wrappers of myelin sheaths. \u0000Results. The pathology of neurons has been observed both at the optical and ultrastructural levels. It is characterized by a decrease in nuclei, cell death, thinning of myelin sheaths and demyelination. The dose of poisoning correlates with the degree of destruction of neurons: with an increase in the dose of dioxin, changes become more significant. The number of synaptic contacts decreases but there is a significant increase in their average length. \u0000Conclusions. The processes of demyelination, impaired cellular respiration and destruction of synaptic contacts indicate the ability of dioxin to indirectly cause accelerated aging of neurons and their death (apoptosis).","PeriodicalId":74228,"journal":{"name":"Morphology (Dordrecht, Netherlands)","volume":"20 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73910148","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective to study the valves of the deep dorsal vein of the human penis. Material and methods. The study of deep dorsal vein valves in 150 men was carried out using macroscopic and microscopic methods. The work was performed on autopsy material. 47 trunks of the deep dorsal vein isolated using magnifying optics х3,5 from the coronal sulcus to the prostatic venous plexus and 103 fragments of the vein in cross section directly distal to the supporting ligament were studied. We used histological painting coloring with hematoxylin-eosin, funcionam with fuchsin and Mallory. The obtained images of valves in longitudinal and cross sections were subjected to photoregistration and archiving for further detailed study and analysis. Results. As a rule, the studied vein has one trunk, but in 7,3% of cases it is represented by 2 trunks. Most often there is a division of the main trunk of the vein. Valves of the deep dorsal vein in the longitudinal section are detected in 89% of observations. On the cross-section, the valve in 36% of cases is detected near the supporting ligament. Valves are represented most often by 2 flaps, at the base of which there is a roller associated with the middle shell of the vein wall. The valves of the deep dorsal vein of the penis have the typical appearance of "pocket" type valves and do not prevent the outflow of venous blood from the cavernous bodies, blocking retrograde blood flow. Conclusions. Valves are a constant component of the deep dorsal vein of the human penis. The structure of the valves indicates that they prevent retrograde blood flow to the cavernous bodies, both at rest and during erection.
{"title":"Macro-microscopic examination of the valves of the deep dorsal vein of the human penis","authors":"A. N. Strelkov, А. Астраханцев, С. С.","doi":"10.17816/morph.110839","DOIUrl":"https://doi.org/10.17816/morph.110839","url":null,"abstract":"Objective to study the valves of the deep dorsal vein of the human penis. \u0000Material and methods. The study of deep dorsal vein valves in 150 men was carried out using macroscopic and microscopic methods. The work was performed on autopsy material. 47 trunks of the deep dorsal vein isolated using magnifying optics х3,5 from the coronal sulcus to the prostatic venous plexus and 103 fragments of the vein in cross section directly distal to the supporting ligament were studied. We used histological painting coloring with hematoxylin-eosin, funcionam with fuchsin and Mallory. The obtained images of valves in longitudinal and cross sections were subjected to photoregistration and archiving for further detailed study and analysis. \u0000Results. As a rule, the studied vein has one trunk, but in 7,3% of cases it is represented by 2 trunks. Most often there is a division of the main trunk of the vein. Valves of the deep dorsal vein in the longitudinal section are detected in 89% of observations. On the cross-section, the valve in 36% of cases is detected near the supporting ligament. Valves are represented most often by 2 flaps, at the base of which there is a roller associated with the middle shell of the vein wall. The valves of the deep dorsal vein of the penis have the typical appearance of \"pocket\" type valves and do not prevent the outflow of venous blood from the cavernous bodies, blocking retrograde blood flow. \u0000Conclusions. Valves are a constant component of the deep dorsal vein of the human penis. The structure of the valves indicates that they prevent retrograde blood flow to the cavernous bodies, both at rest and during erection.","PeriodicalId":74228,"journal":{"name":"Morphology (Dordrecht, Netherlands)","volume":"153 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88164688","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective - study of morphological rearrangements of the bladder and its vascular system in elderly and senile people.Material and methods. Autopsy material in the form of pieces of the bladder wall from 25 men aged 60-80 years was studied using a number of histological, morphometric and statistical techniques. As a control, we used material from 10 persons aged 20-30 years who died as a result of injuries.Results. It was shown that in men in the process of aging in the extraorganic arteries, atherosclerotic changes are revealed, leading to a narrowing of the lumen. In the intraorgan arteries, thickening of the media, hyperelastosis and hyalinosis are observed, which also lead to a reduction in blood flow and are markers of arterial hypertension. A reflection of the adaptation to hemodynamic disorders is the formation of the so-called "closing arteries" with a powerful intimate layer. Over time, in the media of the arteries, as well as in the intima of the "closing vessels", sclerosis grows. The veins of the bladder lose a powerful smooth muscle layer in the wall, undergo sclerosis, which leads to difficulty in blood outflow, aggravating chronic hypoxia. Remodeling of the vascular bed of the bladder leads to detrusor atrophy and degenerative-dysregenerative changes in the urothelium.Conclusion. In the vascular bed of the urinary bladder in elderly and senile men, atherosclerotic and angiotonic changes characteristic of arterial hypertension progress, followed by the development of detrusor atrophy and impaired urothelium regeneration.
{"title":"Morphological reconstruction of the urinary bladder in the process of age involution","authors":"S. Kulikov, И. Ш., А. С.","doi":"10.17816/morph.110831","DOIUrl":"https://doi.org/10.17816/morph.110831","url":null,"abstract":"Objective - study of morphological rearrangements of the bladder and its vascular system in elderly and senile people.Material and methods. Autopsy material in the form of pieces of the bladder wall from 25 men aged 60-80 years was studied using a number of histological, morphometric and statistical techniques. As a control, we used material from 10 persons aged 20-30 years who died as a result of injuries.Results. It was shown that in men in the process of aging in the extraorganic arteries, atherosclerotic changes are revealed, leading to a narrowing of the lumen. In the intraorgan arteries, thickening of the media, hyperelastosis and hyalinosis are observed, which also lead to a reduction in blood flow and are markers of arterial hypertension. A reflection of the adaptation to hemodynamic disorders is the formation of the so-called \"closing arteries\" with a powerful intimate layer. Over time, in the media of the arteries, as well as in the intima of the \"closing vessels\", sclerosis grows. The veins of the bladder lose a powerful smooth muscle layer in the wall, undergo sclerosis, which leads to difficulty in blood outflow, aggravating chronic hypoxia. Remodeling of the vascular bed of the bladder leads to detrusor atrophy and degenerative-dysregenerative changes in the urothelium.Conclusion. In the vascular bed of the urinary bladder in elderly and senile men, atherosclerotic and angiotonic changes characteristic of arterial hypertension progress, followed by the development of detrusor atrophy and impaired urothelium regeneration.","PeriodicalId":74228,"journal":{"name":"Morphology (Dordrecht, Netherlands)","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83444808","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Stem cell (SC) therapy is one of the most perspective methods of clinical medicine; SC containing products are actively investigated in clinical trials, while some of them are already officially approved for treatment in many countries worldwide. So quickly developing direction of modern medicine should be properly reflected in educational programs of medical universities, providing basic understanding of SC subtypes, their properties and potential risks. The purpose of this review is to perform comparative analysis of SC types, methods of their procurement and perspectives of their employment. SCs could be divided into groups according to the age of the donor organism. Embryonic SCs are isolated from blastocyst, obtained as a result of extracorporeal fertilization, cloning, semicloning or parthenogenesis (androgenetic and gynogenetic SCs). Fetal SCs could be isolated from embryonic and fetal tissues before the birth or from miscarriages and abortion material (including ectopic pregnancy). Among fetal there is and especial group of perinatal extraembryonic SCs which are obtained from extraembryonic organs (umbilical cord, amnion, placenta) after the birth; among them hematopoietic, mesenchymal, epithelial and decidual cells are distinguished. Adult (somatic, tissue specific) SCs could be isolated from different tissues and organs of adult organism throughout the life; their properties depend on the place of their localization and age of the donor. Additionally, SCs could be created artificially from mature cells by modification of gene expression; they are united in the group of induced pluripotent SCs. Every group of SCs is not homogenous and has its advances and drawbacks, analyzed in this review. Also, application of exosomes produced by stem cells as an alternative of cellular therapy is considered.
{"title":"Comparative characteristics of human stem cells","authors":"O. Pototskaya, K. Shevchenko","doi":"10.17816/morph.110833","DOIUrl":"https://doi.org/10.17816/morph.110833","url":null,"abstract":"Stem cell (SC) therapy is one of the most perspective methods of clinical medicine; SC containing products are actively investigated in clinical trials, while some of them are already officially approved for treatment in many countries worldwide. So quickly developing direction of modern medicine should be properly reflected in educational programs of medical universities, providing basic understanding of SC subtypes, their properties and potential risks. The purpose of this review is to perform comparative analysis of SC types, methods of their procurement and perspectives of their employment. SCs could be divided into groups according to the age of the donor organism. Embryonic SCs are isolated from blastocyst, obtained as a result of extracorporeal fertilization, cloning, semicloning or parthenogenesis (androgenetic and gynogenetic SCs). Fetal SCs could be isolated from embryonic and fetal tissues before the birth or from miscarriages and abortion material (including ectopic pregnancy). Among fetal there is and especial group of perinatal extraembryonic SCs which are obtained from extraembryonic organs (umbilical cord, amnion, placenta) after the birth; among them hematopoietic, mesenchymal, epithelial and decidual cells are distinguished. Adult (somatic, tissue specific) SCs could be isolated from different tissues and organs of adult organism throughout the life; their properties depend on the place of their localization and age of the donor. Additionally, SCs could be created artificially from mature cells by modification of gene expression; they are united in the group of induced pluripotent SCs. Every group of SCs is not homogenous and has its advances and drawbacks, analyzed in this review. Also, application of exosomes produced by stem cells as an alternative of cellular therapy is considered.","PeriodicalId":74228,"journal":{"name":"Morphology (Dordrecht, Netherlands)","volume":"50 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90655699","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-08-18DOI: 10.1007/s11525-022-09398-w
Irene Lami, Joost van de Weijer
{"title":"Compound-internal anaphora: evidence from acceptability judgements on Italian argumental compounds","authors":"Irene Lami, Joost van de Weijer","doi":"10.1007/s11525-022-09398-w","DOIUrl":"https://doi.org/10.1007/s11525-022-09398-w","url":null,"abstract":"","PeriodicalId":74228,"journal":{"name":"Morphology (Dordrecht, Netherlands)","volume":"13 1","pages":"359 - 388"},"PeriodicalIF":0.0,"publicationDate":"2022-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86633640","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-08-01DOI: 10.17816/1026-3543-2021-159-2-63-70
O. Zlobina, A. N. Ivanov, T. V. Milashevskaya, Valeria Yu. Seryogina, I. Bugaeva
AIM: To compare morphological changes that occur in renal tissue, as a result of exposure to various models of light desynchronosis. MATERIAL AND METHODS: This study was conducted on 48 white rats. Three experimental groups were exposed to light for 21 days. The LL (0:24) model was studied in the first group, while the LD 18:6 and 12:10 models were studied in the second and third groups, respectively. The control group was kept in natural conditions all through the experiment. The animals were placed under anesthesia with a combination of Telazol (ZoetisInc, USA) and Xylanit (Nita-farm, Russia). Afterward, their right kidney was removed. The samples obtained were prepared according to the standard method. Statistical processing was performed using the package of applied statistical programs "STATISTICA 10" (StatSoft , USA). RESULTS: Morphological disorders of the renal tissue were observed in the three experimental groups. In the first experimental group, there was a significant segmentation of the glomeruli, accompanied by dystrophic changes in the renal tubules. In the second experimental group, glomerular segmentation was more pronounced. In the renal tissue of animals of the third experimental group, the disorders were highly observable, and the sclerotized segment is noted. Changes in morphometric indicators were significant across all experimental groups. CONCLUSION: Desynchronosis harms the renal tissue by causing changes in its morphology. The most significant disorders characterized by sclerosis were observed in the kidneys of animals in the third experimental group.
{"title":"Comparative analysis of morphological changes in renal tissue under the influence of light desynchronosis","authors":"O. Zlobina, A. N. Ivanov, T. V. Milashevskaya, Valeria Yu. Seryogina, I. Bugaeva","doi":"10.17816/1026-3543-2021-159-2-63-70","DOIUrl":"https://doi.org/10.17816/1026-3543-2021-159-2-63-70","url":null,"abstract":"AIM: To compare morphological changes that occur in renal tissue, as a result of exposure to various models of light desynchronosis. \u0000MATERIAL AND METHODS: This study was conducted on 48 white rats. Three experimental groups were exposed to light for 21 days. The LL (0:24) model was studied in the first group, while the LD 18:6 and 12:10 models were studied in the second and third groups, respectively. The control group was kept in natural conditions all through the experiment. \u0000The animals were placed under anesthesia with a combination of Telazol (ZoetisInc, USA) and Xylanit (Nita-farm, Russia). Afterward, their right kidney was removed. The samples obtained were prepared according to the standard method. Statistical processing was performed using the package of applied statistical programs \"STATISTICA 10\" (StatSoft , USA). \u0000RESULTS: Morphological disorders of the renal tissue were observed in the three experimental groups. In the first experimental group, there was a significant segmentation of the glomeruli, accompanied by dystrophic changes in the renal tubules. In the second experimental group, glomerular segmentation was more pronounced. In the renal tissue of animals of the third experimental group, the disorders were highly observable, and the sclerotized segment is noted. Changes in morphometric indicators were significant across all experimental groups. \u0000CONCLUSION: Desynchronosis harms the renal tissue by causing changes in its morphology. The most significant disorders characterized by sclerosis were observed in the kidneys of animals in the third experimental group.","PeriodicalId":74228,"journal":{"name":"Morphology (Dordrecht, Netherlands)","volume":"67 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76292708","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-08-01DOI: 10.17816/1026-3543-2021-159-2-37-46
R. Mustafin, E. Khusnutdinova
Recently, a lot of data has been gathered which demonstrates neurogenesis in the brain of adult humans. In genetics, findings have been obtained that not only prove, but also elucidate the molecular mechanisms of neurogenesis. In some publications, however, morphology disputes neuronal renewal in adulthood. Therefore, this review presents the modern achievements of epigenetics, morphology, and physiology, which confirm and characterize postnatal neurogenesis in detail. We suggest that the introduction of molecular genetic technologies into morphological studies will be the starting point for the integration of these areas, complementing each other for the introduction of targeted therapy in clinical practice. Numerous evidence has been obtained of the presence of postnatal neurogenesis in adult humans in studies using bromodeoxyuridine, a carbon isotope of 14C, and 3H-thymidine, in comparative analyses of experimental data from animals. Neuronal stem cells, represented by radial glia present in the subventricular and subgranular zones of the human brain, are morphologically similar to neuroepithelial cells. They express marker proteins for astrocytes, which suggests that the proliferation of neuroglia found in adults can also indicate the regeneration of neurons. To prove this, further studies are required, with the exact identification of newly-formed cells, using specific molecular markers, and data from modern epigenetics. The integration of molecular genetic methods into morphology will facilitate not only the accurate determination of the classification of cells to a specific subpopulation but also to study the effects of various agents on the proliferation of neurons in the adult brain.
{"title":"Postnatal neurogenesis in the human brain","authors":"R. Mustafin, E. Khusnutdinova","doi":"10.17816/1026-3543-2021-159-2-37-46","DOIUrl":"https://doi.org/10.17816/1026-3543-2021-159-2-37-46","url":null,"abstract":"Recently, a lot of data has been gathered which demonstrates neurogenesis in the brain of adult humans. In genetics, findings have been obtained that not only prove, but also elucidate the molecular mechanisms of neurogenesis. In some publications, however, morphology disputes neuronal renewal in adulthood. Therefore, this review presents the modern achievements of epigenetics, morphology, and physiology, which confirm and characterize postnatal neurogenesis in detail. We suggest that the introduction of molecular genetic technologies into morphological studies will be the starting point for the integration of these areas, complementing each other for the introduction of targeted therapy in clinical practice. Numerous evidence has been obtained of the presence of postnatal neurogenesis in adult humans in studies using bromodeoxyuridine, a carbon isotope of 14C, and 3H-thymidine, in comparative analyses of experimental data from animals. Neuronal stem cells, represented by radial glia present in the subventricular and subgranular zones of the human brain, are morphologically similar to neuroepithelial cells. They express marker proteins for astrocytes, which suggests that the proliferation of neuroglia found in adults can also indicate the regeneration of neurons. To prove this, further studies are required, with the exact identification of newly-formed cells, using specific molecular markers, and data from modern epigenetics. The integration of molecular genetic methods into morphology will facilitate not only the accurate determination of the classification of cells to a specific subpopulation but also to study the effects of various agents on the proliferation of neurons in the adult brain.","PeriodicalId":74228,"journal":{"name":"Morphology (Dordrecht, Netherlands)","volume":"206 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73623221","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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