Pub Date : 2025-07-17DOI: 10.1007/s12565-025-00872-z
Sedat Alp Pinar, Joseph J Morrow, Chia Yew Kong
While laparoscopy has become the gold standard for many abdominal surgical procedures, it has a steeper learning curve compared to an open surgical approach. Body donor (cadaveric) models (BDM) present a high-fidelity model for laparoscopic surgical training. There are a variety of models available from fresh-frozen models to soft-embalmed models using multiple proprietary preparation solutions. There remains uncertainty surrounding the models' relative strengths and weaknesses. This study aims to evaluate the different body donor models used in postgraduate laparoscopic surgical training. A systematic search was conducted across Medline, Embase, ClinicalTrials.gov, and Cochrane to identify articles relevant to postgraduate laparoscopic training using HBD following the PRISMA guidelines. A narrative review themed on HBD feasibility, validity, and educational utility in laparoscopic surgical training. PROSPERO Registration: NIHR CRD42023437230. Fifty-five studies were included. BDM in general were perceived as authentic and of high educational value. Soft embalmed models (e.g., Thiel®, Genelyn®, modified Larssen®), were reported to be feasible and possess high face validity despite embalming and had advantages over fresh frozen body donors (FFBDs), including reusability, cost-effectiveness, and better odor satisfaction. Comparative studies reported a preference of human body donor models over other simulation methods due to its high fidelity. Body donor models including soft embalmed models provide high-fidelity laparoscopic training environments well perceived by trainees regardless of preservation or tissue fixation. Significant research gaps remain; head-to-head comparative studies between the different models remain sparse as well as data on non-educational aspects such as formal cost-utility analysis and ecological impact.
{"title":"A systematic review of the use of human body donor models for postgraduate laparoscopic surgical training.","authors":"Sedat Alp Pinar, Joseph J Morrow, Chia Yew Kong","doi":"10.1007/s12565-025-00872-z","DOIUrl":"10.1007/s12565-025-00872-z","url":null,"abstract":"<p><p>While laparoscopy has become the gold standard for many abdominal surgical procedures, it has a steeper learning curve compared to an open surgical approach. Body donor (cadaveric) models (BDM) present a high-fidelity model for laparoscopic surgical training. There are a variety of models available from fresh-frozen models to soft-embalmed models using multiple proprietary preparation solutions. There remains uncertainty surrounding the models' relative strengths and weaknesses. This study aims to evaluate the different body donor models used in postgraduate laparoscopic surgical training. A systematic search was conducted across Medline, Embase, ClinicalTrials.gov, and Cochrane to identify articles relevant to postgraduate laparoscopic training using HBD following the PRISMA guidelines. A narrative review themed on HBD feasibility, validity, and educational utility in laparoscopic surgical training. PROSPERO Registration: NIHR CRD42023437230. Fifty-five studies were included. BDM in general were perceived as authentic and of high educational value. Soft embalmed models (e.g., Thiel<sup>®</sup>, Genelyn<sup>®</sup>, modified Larssen<sup>®</sup>), were reported to be feasible and possess high face validity despite embalming and had advantages over fresh frozen body donors (FFBDs), including reusability, cost-effectiveness, and better odor satisfaction. Comparative studies reported a preference of human body donor models over other simulation methods due to its high fidelity. Body donor models including soft embalmed models provide high-fidelity laparoscopic training environments well perceived by trainees regardless of preservation or tissue fixation. Significant research gaps remain; head-to-head comparative studies between the different models remain sparse as well as data on non-educational aspects such as formal cost-utility analysis and ecological impact.</p>","PeriodicalId":7816,"journal":{"name":"Anatomical Science International","volume":" ","pages":""},"PeriodicalIF":1.7,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144658170","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-15DOI: 10.1007/s12565-025-00871-0
Denise Bonente, Tiziana Tamborrino, Niccolò Fagni, Sandra Bracco, Sara Leonini, Sara Ottolenghi, Virginia Barone, Eugenio Bertelli
The superior oblique muscle tendon is known to bend in the anterior orbit around a cartilaginous trochlea. The site where the tendon bends is frequently interested by the presence of a small depression, the trochlear fovea, and/or the trochlear spine. Exact topography, size and frequency of these items are still undetermined. For this purpose, we studied 120 orbits of individuals that underwent computed tomography for pathologies not involving the anterior orbit. We detected the presence of the trochlear spine in 10% of orbits and we determined its location and size. We also observed the presence of two tubercles (TT1 and TT2), with distinct positions relative to the tendon. TT1 was present in 5% of orbits and was located on the same spot of the spine differing from the latter only for its morphology. TT2 lied in a more advanced position and it was rarer (1,67% of orbits). The spine and the first type of tubercle were located above and behind the tendon reflection; the second tubercle lied below and ahead of the tendon reflection. A distinct trochlear fovea was detected in 25.83% of orbits and lied 3.42 ± 0.97 mm behind the orbital rim. Fovea diameters were 4.16 ± 1.08 mm × 3.84 ± 0.97 mm. In conclusion we demonstrate that in the anterior orbit a bony process is present in at least 15% or orbits. It is a note of interest for strabismus surgery when it is necessary to intervene on the superior oblique muscle or when it is needed access to the medial orbital wall.
已知上斜肌肌腱在软骨滑车周围的前眶内弯曲。肌腱弯曲的部位通常会出现小凹陷、滑车中央窝和/或滑车脊柱。这些项目的确切地形、大小和频率仍未确定。为此,我们研究了120例患者的眼眶,这些患者接受了不涉及前眼眶的病变的计算机断层扫描。我们在10%的眼眶中检测到滑车脊柱的存在并确定了它的位置和大小。我们还观察到两个结节(TT1和TT2)的存在,相对于肌腱有不同的位置。TT1出现在5%的眼眶中,位于脊柱的同一位置,与后者仅在形态上有所不同。TT2位于更靠前的位置,它是罕见的(1.67%的轨道)。脊柱和第一类结节位于肌腱反射的上方和后方;第二个结节位于肌腱反射的下方和前方。在25.83%的眶内发现明显的滑车中央窝,位于眶缘后3.42±0.97 mm。中心凹直径为4.16±1.08 mm × 3.84±0.97 mm。总之,我们证明在前眼眶中至少有15%的眼眶存在骨突。在斜视手术中,当需要介入上斜肌或需要进入眶内壁时,这是一个值得注意的问题。
{"title":"Radiological anatomy of the trochlear spine and associated bony structures around the superior oblique tendon: a CT-based study.","authors":"Denise Bonente, Tiziana Tamborrino, Niccolò Fagni, Sandra Bracco, Sara Leonini, Sara Ottolenghi, Virginia Barone, Eugenio Bertelli","doi":"10.1007/s12565-025-00871-0","DOIUrl":"https://doi.org/10.1007/s12565-025-00871-0","url":null,"abstract":"<p><p>The superior oblique muscle tendon is known to bend in the anterior orbit around a cartilaginous trochlea. The site where the tendon bends is frequently interested by the presence of a small depression, the trochlear fovea, and/or the trochlear spine. Exact topography, size and frequency of these items are still undetermined. For this purpose, we studied 120 orbits of individuals that underwent computed tomography for pathologies not involving the anterior orbit. We detected the presence of the trochlear spine in 10% of orbits and we determined its location and size. We also observed the presence of two tubercles (TT<sub>1</sub> and TT<sub>2</sub>), with distinct positions relative to the tendon. TT<sub>1</sub> was present in 5% of orbits and was located on the same spot of the spine differing from the latter only for its morphology. TT<sub>2</sub> lied in a more advanced position and it was rarer (1,67% of orbits). The spine and the first type of tubercle were located above and behind the tendon reflection; the second tubercle lied below and ahead of the tendon reflection. A distinct trochlear fovea was detected in 25.83% of orbits and lied 3.42 ± 0.97 mm behind the orbital rim. Fovea diameters were 4.16 ± 1.08 mm × 3.84 ± 0.97 mm. In conclusion we demonstrate that in the anterior orbit a bony process is present in at least 15% or orbits. It is a note of interest for strabismus surgery when it is necessary to intervene on the superior oblique muscle or when it is needed access to the medial orbital wall.</p>","PeriodicalId":7816,"journal":{"name":"Anatomical Science International","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144641579","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-15DOI: 10.1007/s12565-025-00870-1
Mugurel Constantin Rusu, Răzvan Costin Tudose
Different head and neck anatomical structures, such as the temporomandibular joint, carotid arteries and their branches, styloid process, hyoid and thyroid cartilage, are subjected to anatomical variations. A range of novel and rare anatomical variants were found during the anatomical exploration of a DICOM file. The archived angioCT file of a 63-year-old male was examined anatomically. There were no pathological processes or other artefacts to distort the anatomical patterns. The imprint of Farabeuf's knocker (posterior zygomatic tubercle) on the posterior side of the right mandibular condyle was found. This is an anatomical novelty. Rare neck variations were found: a right-tilted and collapsed hyoid bone over the thyroid cartilage and the agenesis of the left superior horn of this cartilage. Variations of the external carotid arteries' branches were observed. A right thyrolingual trunk gave off a superior thyroid artery that supplied both thyroid lobes with distinctive right and left branches, the opposite superior thyroid artery being absent. On both sides, the superficial temporal artery coursed over the temporomandibular joints. The right internal carotid artery coiled immediately beneath the skull base. It is recommended that CT scans be carefully explored, as various concomitant anatomical variations, including rare or previously unreported findings, may be encountered.
{"title":"A condylar imprint of Farabeuf's knocker and associated cervical variants.","authors":"Mugurel Constantin Rusu, Răzvan Costin Tudose","doi":"10.1007/s12565-025-00870-1","DOIUrl":"https://doi.org/10.1007/s12565-025-00870-1","url":null,"abstract":"<p><p>Different head and neck anatomical structures, such as the temporomandibular joint, carotid arteries and their branches, styloid process, hyoid and thyroid cartilage, are subjected to anatomical variations. A range of novel and rare anatomical variants were found during the anatomical exploration of a DICOM file. The archived angioCT file of a 63-year-old male was examined anatomically. There were no pathological processes or other artefacts to distort the anatomical patterns. The imprint of Farabeuf's knocker (posterior zygomatic tubercle) on the posterior side of the right mandibular condyle was found. This is an anatomical novelty. Rare neck variations were found: a right-tilted and collapsed hyoid bone over the thyroid cartilage and the agenesis of the left superior horn of this cartilage. Variations of the external carotid arteries' branches were observed. A right thyrolingual trunk gave off a superior thyroid artery that supplied both thyroid lobes with distinctive right and left branches, the opposite superior thyroid artery being absent. On both sides, the superficial temporal artery coursed over the temporomandibular joints. The right internal carotid artery coiled immediately beneath the skull base. It is recommended that CT scans be carefully explored, as various concomitant anatomical variations, including rare or previously unreported findings, may be encountered.</p>","PeriodicalId":7816,"journal":{"name":"Anatomical Science International","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144635935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-14DOI: 10.1007/s12565-025-00866-x
Motokazu Uchigashima, Takayasu Mikuni
High-precision mapping of endogenous proteins is essential for understanding the molecular mechanism underlying neuronal functions in the brain. The SLENDR (single-cell labeling of endogenous proteins by clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9-mediated homology-directed repair) technique provides single-cell endogenous protein labeling with genetically encoded tags within the mammalian brain through precise genome editing via homology-directed repair (HDR). This technique is based on the introduction of HDR-mediated genome editing into neuronal progenitors in embryonic brains by in utero electroporation. Subsequent histological analyses enable high-resolution interrogation of the subcellular distribution of endogenous proteins within a single neuron using conventional fluorescent microscopy. Here, we describe a step-by-step protocol for the SLENDR technique to label endogenous proteins with genetically encoded tags in single pyramidal cells of the mouse primary somatosensory cortex. This protocol would be helpful to visualize the molecular organization underlying biological processes at single-neuron levels in the brain, such as signal processing from synaptic inputs to neuronal outputs across different scales.
{"title":"Single-cell endogenous protein labeling via CRISPR-Cas9-mediated genome editing in the mouse brain","authors":"Motokazu Uchigashima, Takayasu Mikuni","doi":"10.1007/s12565-025-00866-x","DOIUrl":"10.1007/s12565-025-00866-x","url":null,"abstract":"<div><p>High-precision mapping of endogenous proteins is essential for understanding the molecular mechanism underlying neuronal functions in the brain. The SLENDR (single-cell labeling of endogenous proteins by clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9-mediated homology-directed repair) technique provides single-cell endogenous protein labeling with genetically encoded tags within the mammalian brain through precise genome editing via homology-directed repair (HDR). This technique is based on the introduction of HDR-mediated genome editing into neuronal progenitors in embryonic brains by in utero electroporation. Subsequent histological analyses enable high-resolution interrogation of the subcellular distribution of endogenous proteins within a single neuron using conventional fluorescent microscopy. Here, we describe a step-by-step protocol for the SLENDR technique to label endogenous proteins with genetically encoded tags in single pyramidal cells of the mouse primary somatosensory cortex. This protocol would be helpful to visualize the molecular organization underlying biological processes at single-neuron levels in the brain, such as signal processing from synaptic inputs to neuronal outputs across different scales.</p></div>","PeriodicalId":7816,"journal":{"name":"Anatomical Science International","volume":"100 :","pages":"579 - 590"},"PeriodicalIF":1.7,"publicationDate":"2025-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144625288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-09DOI: 10.1007/s12565-025-00868-9
Kazunori Toida, Keita Satoh, Haruyo Yamanishi, Yukari Minami-Ogawa, Simone N. T. Kurial, Emi Kiyokage
In this article, we will introduce the significance of correlative light and electron microscopy analyses, an integrated morphological analysis method that directly combines laser and electron microscopes. This protocol comprehensively instructs the appropriate methods for the visualization of genetically labeled neurons in mice using digitalized electron microscopes. We wish to consider with the readers the importance and functional potential of electron microscopic analysis for medical and biological applications, especially for neurobiological applications.
{"title":"Correlative light and electron microscopy analysis for neurobiological applications","authors":"Kazunori Toida, Keita Satoh, Haruyo Yamanishi, Yukari Minami-Ogawa, Simone N. T. Kurial, Emi Kiyokage","doi":"10.1007/s12565-025-00868-9","DOIUrl":"10.1007/s12565-025-00868-9","url":null,"abstract":"<div><p>In this article, we will introduce the significance of correlative light and electron microscopy analyses, an integrated morphological analysis method that directly combines laser and electron microscopes. This protocol comprehensively instructs the appropriate methods for the visualization of genetically labeled neurons in mice using digitalized electron microscopes. We wish to consider with the readers the importance and functional potential of electron microscopic analysis for medical and biological applications, especially for neurobiological applications.</p></div>","PeriodicalId":7816,"journal":{"name":"Anatomical Science International","volume":"100 :","pages":"455 - 464"},"PeriodicalIF":1.7,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144590290","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-09DOI: 10.1007/s12565-025-00869-8
Chitoshi Takayama, Tsukasa Yafuso
In the mature central nervous system (CNS), γ-aminobutyric acid (GABA) and glycine (Gly) are predominant inhibitory neurotransmitters that negatively regulate neural activities. In contrast, GABA mediates membrane potential depolarization during development, and GABA/Gly become excitatory after nerve injury because of the high intracellular Cl- concentration induced by low expression of K+, Cl- cotransporter 2 (KCC2), which transports Cl- out of neurons. Many studies have reported that during CNS development, GABAergic excitatory action might play crucial roles in neurogenesis through Ca2+ influx. Nevertheless, its involvement in neurogenesis has not been proven because the CNS can develop normally without GABAergic signals. Recently, two research groups demonstrated that low level of KCC2 (i.e., GABA/Gly excitation) after nerve injury is involved in axonal regeneration and in enhancement of functional recovery. In this manuscript, we review GABA/Gly excitation and introduce recent findings describing its involvement in axonal regeneration.
{"title":"Acceleration of axonal regeneration by GABA/Gly excitation.","authors":"Chitoshi Takayama, Tsukasa Yafuso","doi":"10.1007/s12565-025-00869-8","DOIUrl":"https://doi.org/10.1007/s12565-025-00869-8","url":null,"abstract":"<p><p>In the mature central nervous system (CNS), γ-aminobutyric acid (GABA) and glycine (Gly) are predominant inhibitory neurotransmitters that negatively regulate neural activities. In contrast, GABA mediates membrane potential depolarization during development, and GABA/Gly become excitatory after nerve injury because of the high intracellular Cl<sup>-</sup> concentration induced by low expression of K<sup>+</sup>, Cl<sup>-</sup> cotransporter 2 (KCC2), which transports Cl<sup>-</sup> out of neurons. Many studies have reported that during CNS development, GABAergic excitatory action might play crucial roles in neurogenesis through Ca<sup>2+</sup> influx. Nevertheless, its involvement in neurogenesis has not been proven because the CNS can develop normally without GABAergic signals. Recently, two research groups demonstrated that low level of KCC2 (i.e., GABA/Gly excitation) after nerve injury is involved in axonal regeneration and in enhancement of functional recovery. In this manuscript, we review GABA/Gly excitation and introduce recent findings describing its involvement in axonal regeneration.</p>","PeriodicalId":7816,"journal":{"name":"Anatomical Science International","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144590289","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-08DOI: 10.1007/s12565-025-00859-w
Sven Hildebrand, Johannes Franz, Shubharthi Sengupta, Anna Schueth, Andreas Herrler, Alard Roebroeck
The performance of many optical tissue clearing protocols has considerably improved in the last few years, so that now even notoriously difficult specimen such as highly myelinated human brain tissue can be rendered highly transparent. However, optical tissue clearing is still routinely performed on relatively small samples, especially in the case of the human brain. Recent advances in histological tissue processing now allow scaling up the clearing process considerably towards much larger samples. Yet so far, these methods can have considerable drawbacks in their feasibility to be implemented routinely, especially in smaller laboratories. Here, we present an updated version of our MASH protocol, which allows optical tissue clearing of very large human brain tissue samples and labelling of angio- and cytoarchitecture therein. This pipeline is cost-efficient and easy to implement, so that even smaller labs can apply it at scale. At the same time, the use of rapid prototyping using 3D printing to create custom clearing equipment is versatile enough to be adjusted to other optical tissue clearing methods than the one used in this study (e.g., aqueous methods such as CUBIC or other solvent-based methods of the DISCO family), sample sizes or tissue types. Our pipeline has, therefore, the potential to advance optical tissue clearing and labelling of large human tissue samples towards a more robust and routine implementation in the blooming field of 3D histology.