Abstract:Structure and length of transitional zone in the dog's external carotid artery was documented. Six normal adult male dogs were studied. The specimens were processed in the routine way by light and electron microscopy. It was established that the transitional zone with 17-mm length contains parallel and fenestrated elastic fibres. In the transitional zone, the elastic fibres in the extracellular space were greater in number than collagen fibres. However, in the non-transitional zone, the rows of smooth muscle c… Show more
“…In addition to elastic arteries being closer to the heart and muscular arteries being further away, there are known transition points along a given arterial pathway where there is a substantial increase in wave speed and distinct change in morphological features from one artery to the next; this indicates a transition from predominantly elastic to more muscular arteries. These points are at the distal ends of the axillary artery for the upper limbs (Bjarnegård & Länne, 2010) and the abdominal aorta for the lower limbs (Latham et al., 1985), and 1 cm from the origin of the external carotid artery for the head and neck region (Nowrozani & Zareiyan, 2011) [we here assume the same distance for the internal carotid artery, consistent with its classification as a muscular artery (Rees, 1968)]. Using this, we propose a ‘transition distance index’ (TDI) of an artery as a surrogate marker for its degree of elasticity/muscularity.…”
“…In addition to elastic arteries being closer to the heart and muscular arteries being further away, there are known transition points along a given arterial pathway where there is a substantial increase in wave speed and distinct change in morphological features from one artery to the next; this indicates a transition from predominantly elastic to more muscular arteries. These points are at the distal ends of the axillary artery for the upper limbs (Bjarnegård & Länne, 2010) and the abdominal aorta for the lower limbs (Latham et al., 1985), and 1 cm from the origin of the external carotid artery for the head and neck region (Nowrozani & Zareiyan, 2011) [we here assume the same distance for the internal carotid artery, consistent with its classification as a muscular artery (Rees, 1968)]. Using this, we propose a ‘transition distance index’ (TDI) of an artery as a surrogate marker for its degree of elasticity/muscularity.…”
“…Moving along the length of each artery from the heart (caudal region) toward the head (cranial region) there is an arterial narrowing and a distinct transitional zone in which the elastic wall is replaced by a muscular type [ 25 ], resulting in the caudal region of the artery having a larger elastin content and the cranial region a more collagenous structure. Collagen and elastin are the main components responsible for the mechanical behavior of the arterial wall [ 26 , 27 ] and alterations in the collagen to elastin ratio help maintain blood pressure and regulate blood flow across changes in artery diameter [ 25 , 28 ]. An imaging technique that quantitatively assess the anatomical differences in the collagen and elastin content of native artery would provide direct biochemical information and also infer differences in the functional properties of the tissue.…”
Novel diagnostic tools with the ability to monitor variations in biochemical composition and provide benchmark indicators of vascular tissue maturation are needed to create functional tissue replacements. We investigated the ability of fiber-based, label-free multispectral fluorescent lifetime imaging (FLIm) to quantify the anatomical variations in biochemical composition of native carotid arteries and validated these results against biochemical assays. FLIm-derived parameters in spectral band 415–455 nm correlated with tissue collagen content (R2 = 0.64) and cell number (R2 = 0.61) and in spectral band 465–553 nm strongly correlated with elastin content (R2 = 0.89). These results suggest that FLIm holds great potential for assessing vascular tissue maturation and functional properties based on tissue autofluorescence.
“…28,36,37 However, reports on enzootic calcinosis in muscular arteries are uncommon. 46 In muscular arteries, such as the external carotid artery, 30 mineralization is not observed in the intima; it is seen only in the media. In sheep poisoned by Nierembergia veitchii , the intima of external carotid arteries showed hyperplasia without mineralization, and the media was mineralized with large areas of osteochondroid metaplasia in the advanced stages of the disease.…”
Vascular mineralization is a hallmark of enzootic calcinosis. Histopathological, ultrastructural, and immunohistochemical investigations were performed on the external carotid arteries of seven sheep naturally poisoned by Nierembergia veitchii. Histologically, moderate to marked hyperplasia of the tunica intima was observed without mineralization. The tunica media exhibited mild to severe mineralization and osteochondroid metaplasia. Sheep with enzootic calcinosis showed arterial overexpression of osteopontin and tissue-nonspecific alkaline phosphatase and immunolabeling for osteonectin and osteocalcin in both intima and media layers of the tested arteries. The main ultrastructural finding in the tunica media was a marked phenotypic change of vascular smooth muscle cells from a contractile phenotype (VSMC-C) into a synthetic phenotype (VSMC-S). In the tunica media, VSMC-S produced matrix and extracellular vesicles, forming mineralizable granules associated with arterial mineralization. VSMC-S were also present in the tunica intima, but matrix and extracellular vesicles and mineralization were not observed. The absence of matrix and extracellular vesicles in the intimal hyperplasia, even in the presence of noncollagenous bone proteins, tissue-nonspecific alkaline phosphatase, and vitamin D receptors, reinforces the hypothesis that the presence of matrix and extracellular vesicles are crucial for the development of vascular mineralization in enzootic calcinosis. It is proposed that the two different VSMC-S phenotypes in calcinosis are due to the expression of at least two genetically different types of these cells induced by the action of 1,25(OH)2D3.
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