Abstract:The tongue of an adult degu was examined by light and scanning electron microscopy. It consists of an apex, corpus, and radix and contains a lingual prominence. The aim of this study was to describe the course of muscle fascicles of the proper lingual muscle, the presence and nature of the lingual salivary glands, and particularly the appearance and distribution of the lingual papillae. Three major types of papillae have been observed: filiform, conical, and vallate. The dorsal surface of the lingual apex exte… Show more
“…The number of vallate papillae in rodents has been found to range from one to four. The lesser bamboo rat had two vallate papillae, similar to those in its spalacid relatives (Kilinc et al, ; Wannaprasert, ), caviids (Ciena et al, ; Emura et al, ; Santos et al, ; Watanabe et al, ) and degu (Cizek, Hamouzova, Jekl, Kvapil, & Tichy, ). Only a single papilla is observed in the mouse (Kobayashi et al, ), bank vole (Jackowiak & Godynicki, ) and lab rat (Reginato et al, ).…”
Section: Discussionmentioning
confidence: 76%
“…Weber's glands, posteriorly adjacent to Ebner's gland, deliver their products onto the surface of the lingual radix. These glands in the lesser bamboo rat were of the pure mucous type, like in the American beaver (Shindo et al, ) and large bamboo rat (Wannaprasert, ), but in contrast to the seromucous type found in the rat (Nagato, Ren, Toh, & Tandler, ), degu (Cizek et al, ) and Persian squirrel (Sadeghinezhad et al, ). Mucus is a viscous, slippery substance so it can facilitate deglutition of hard and dry food, prevent damage to the lingual epithelium and lubricate tongue movement through the intraoral structures.…”
Section: Discussionmentioning
confidence: 96%
“…These morphologies of the vallate papillae and their surroundings in the lesser bamboo rat are similar to those observed in its close relative, the large bamboo rat (Wannaprasert, ). It is noteworthy that in many rodents, such as the Patagonian cavy (Emura et al, ), agouti (Ciena et al, ), degu (Cizek et al, ) and guinea pig (Ciena et al, ), grooves bordering the vallate papillae are interrupted, forming separate parallel grooves. From an anatomical point of view, because vallate taste buds are normally buried in the papillary sidewall and their taste pores open into the trench, the vallate papilla with a complete moat perhaps provides a larger occupied area of taste buds than that of a comparable size with an incomplete moat.…”
The first detailed morphological description of the tongue and lingual papillae of the lesser bamboo rat, a fossorial rodent distributed in Indochina, is presented. Twelve tongues were examined by light, stereo-and scanning electron microscopy. The elongated tongue possessed an intermolar prominence and terminated in a rounded apex with a median sulcus. The dorsal surface of the tongue bores three types of papillae: filiform, fungiform and vallate, the first two of which were also observed on the ventral lingual surface. The filiform papillae varied in form and arrangement depending on the tongue region, although the majority of them were multifurcate, fork-like papillae. The fungiform papillae were randomly scattered among the filiform papillae, with the highest density and number of taste pores (up to 12) at the ventral lingual apex. On the posterior tongue, two oval vallate papillae with numerous taste buds on their lateral epithelium were surrounded by a circumferential trench into which the serous von Ebner's glands' ducts opened. The mucosal surface of the lingual radix was uneven without papillae, but contained mucous openings of Weber's glands. The tongue and lingual papillae of the lesser bamboo rat are similar to those of the large bamboo rat and show structural adaptations to the diet and food manipulation.
“…The number of vallate papillae in rodents has been found to range from one to four. The lesser bamboo rat had two vallate papillae, similar to those in its spalacid relatives (Kilinc et al, ; Wannaprasert, ), caviids (Ciena et al, ; Emura et al, ; Santos et al, ; Watanabe et al, ) and degu (Cizek, Hamouzova, Jekl, Kvapil, & Tichy, ). Only a single papilla is observed in the mouse (Kobayashi et al, ), bank vole (Jackowiak & Godynicki, ) and lab rat (Reginato et al, ).…”
Section: Discussionmentioning
confidence: 76%
“…Weber's glands, posteriorly adjacent to Ebner's gland, deliver their products onto the surface of the lingual radix. These glands in the lesser bamboo rat were of the pure mucous type, like in the American beaver (Shindo et al, ) and large bamboo rat (Wannaprasert, ), but in contrast to the seromucous type found in the rat (Nagato, Ren, Toh, & Tandler, ), degu (Cizek et al, ) and Persian squirrel (Sadeghinezhad et al, ). Mucus is a viscous, slippery substance so it can facilitate deglutition of hard and dry food, prevent damage to the lingual epithelium and lubricate tongue movement through the intraoral structures.…”
Section: Discussionmentioning
confidence: 96%
“…These morphologies of the vallate papillae and their surroundings in the lesser bamboo rat are similar to those observed in its close relative, the large bamboo rat (Wannaprasert, ). It is noteworthy that in many rodents, such as the Patagonian cavy (Emura et al, ), agouti (Ciena et al, ), degu (Cizek et al, ) and guinea pig (Ciena et al, ), grooves bordering the vallate papillae are interrupted, forming separate parallel grooves. From an anatomical point of view, because vallate taste buds are normally buried in the papillary sidewall and their taste pores open into the trench, the vallate papilla with a complete moat perhaps provides a larger occupied area of taste buds than that of a comparable size with an incomplete moat.…”
The first detailed morphological description of the tongue and lingual papillae of the lesser bamboo rat, a fossorial rodent distributed in Indochina, is presented. Twelve tongues were examined by light, stereo-and scanning electron microscopy. The elongated tongue possessed an intermolar prominence and terminated in a rounded apex with a median sulcus. The dorsal surface of the tongue bores three types of papillae: filiform, fungiform and vallate, the first two of which were also observed on the ventral lingual surface. The filiform papillae varied in form and arrangement depending on the tongue region, although the majority of them were multifurcate, fork-like papillae. The fungiform papillae were randomly scattered among the filiform papillae, with the highest density and number of taste pores (up to 12) at the ventral lingual apex. On the posterior tongue, two oval vallate papillae with numerous taste buds on their lateral epithelium were surrounded by a circumferential trench into which the serous von Ebner's glands' ducts opened. The mucosal surface of the lingual radix was uneven without papillae, but contained mucous openings of Weber's glands. The tongue and lingual papillae of the lesser bamboo rat are similar to those of the large bamboo rat and show structural adaptations to the diet and food manipulation.
“…The median groove in the WWCPS was approximately 1 cm long and was found only in the apex. A similar well demarcated median groove in the region of the apex was found in rodents such as the bank vole (Jackowiak and Godynicki 2005 ), porcupine (Karan et al 2011 ), the squirrel (Ünsaldi 2010 ), agouti (Ciena et al 2013 ), hazel dormouse (Wołczuk 2014 ), the Persian squirrel (Sadeghinezhad et al 2018 ), the large bamboo rat (Wannaprasert 2018 ) and at the apex and body of the tongue in the degu (Cizek et al 2016 ). In contrast to wild rats, the median groove was absent in the guinea pig (Kobayashi 1990 ), Patagonian cavy (Emura et al 2011 ) and capybara (Watanabe et al 2013 ).…”
Section: Discussionmentioning
confidence: 99%
“…However, the majority of those studies did not assess gender differences, and differences between wild and laboratory rats. Numerous histological and histochemical studies, as well as scanning electron microscopy (SEM) and TEM, have enabled the identification of significant differences in the microstructure of the lingual surface in other selected rodents of the Rodentia order (Kobayashi 1990 ; Kobayashi et al 1992 ; Grandi et al 1994 ; Stangl and Pfau 1994 ; Whitehead and Kachele 1994 ; Watanabe et al 1997 , 2013 ; Emura et al 1999a , b , 2001 , 2011 ; Jackowiak and Godynicki 2005 ; Ünsaldi 2010 ; Shindo et al 2006 ; Kulawik and Godynicki 2007 ; Toprak and Yilmaz 2007 ; Nonaka et al 2008 ; Cheng et al 2009 ; Kilinc et al 2010 ; Alvarez et al 2011 ; Atalar and Karan 2011 ; Karan et al 2011 ; Abumandour and El-Bakary 2013 ; Ciena et al 2013 , 2017 ; Sakr et al 2013 ; Wołczuk 2014 ; Cizek et al 2016 ; Sadeghinezhad et al 2018 ; Wannaprasert 2018 ).…”
The aim of this study was to characterise the tongue in wild-type rats using several microscopic techniques. Warsaw Wild Captive Pisula Stryjek (WWCPS) rats belong to a lineage of wild-caught rats. The study was carried out on tongues of 15 male and 15 female WWCPS rats. Histological, histochemical and ultrastructural studies were carried out. There were no significant differences between the male and female WWCPS rat tongues. There was a median groove approximately 1 cm long in the apex of the tongue that faded caudally. The intermolar prominence was clearly marked in the distal part of the lingual body. Lingual mechanical papillae located on the surface of the tongue formed four subtypes based on their shape: small filiform papillae, giant filiform papillae, thin elongated filiform papillae and wide filiform papillae. Gustatory papillae formed the second group of papillae and were divided into bud-shaped fungiform papillae, a single vallate papilla surrounded by an incomplete papillary groove and foliate papillae, which were a well-formed and composed of several pairs of folds divided by longitudinal grooves. In the posterior lingual glands (mucoserous and serous), acidic sulphated mucin-secreting cells gave a strong AB pH 2.5 positive reaction, and a positive reaction with the AB pH 1.0 stain for acidic carboxylated mucin. Double AB/PAS staining showed the presence of the majority of mucous cells with predominant of acidic mucins. Positive PAS staining showed the presence of neutral mucin. HDI staining demonstrated a weak positive reaction within Weber’s glands of the WWCPS rat tongue.
The current study aimed to describe the anatomical features of the tongues of two micro‐mammals common in the Egyptian fauna; the Nile grass rat (Arvicathis niloticus), and the Egyptian long‐eared hedgehog (Hemiechinus auritus). The tongues of five adult individuals of each species were excised and processed histologically, histochemically, and morphometrically. Statistical analysis comparing the relative tongue length in both species showed that there was a significant difference, which may correlate with the difference in feeding preferences. Grossly, the Nile grass rat has a dorsal lingual prominence with bifurcated apex while, the long‐eared hedgehog has a median slight elevation with rounded apex. Numerous forms of mechanical and gustatory papillae are scattered along the lingual dorsal epithelium. The histochemical detection of keratin by Holland's trichrome stain showed an intense expression in the case of A. niloticus and mild expression in H. auritus. The framework of the tongue (entoglossum) is supported by either a core of cartilage in H. auritus or bone in A. niloticus which incorporated in the lingual root. The lingual glands also showed marked variation, the Nile grass rat exhibit dense populations of mucous‐secreting glands and lesser populations of serous‐secreting glands, the contrary is true in H. auritus. In conclusion, the micro and macro‐anatomical features of the tongues of both species showed adaptive changes to accommodate the feeding lifestyle. Such type of studies using mammals from different phylogenetic traits and almost have different feeding preferences provide answers to many research questions related to tongue evolution among mammalian vertebrates.
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