Blood collection from the tail of a rat

Techniques for blood collection from the rat include puncture of the heart, retro-orbital plexus, jugular vein, saphenous vein, tail blood vessels, carotid artery, abdominal aorta, and vena cava. Most techniques (except saphenous vein and tail blood vessel puncture) require anesthesia. The following discussion focuses on two methods of blood collection - ventral tail artery puncture and dorsal or lateral tail vein puncture.     

Simple method for locating a suitable venipuncture site on the tail of the Virginia opossum (Didelphis virginiana)

We identified a site suitable for venipuncture on the tail of the Virginia opossum (Didelphis virginiana) that is reliably and easily located. The prominent hemal arch associated with the ventral surface of caudal vertebra 5 serves as an easily palpated anatomical landmark for locating the ventral caudal vein for blood collection. Because this venipuncture site is only thinly covered by fur and visualization of the vein is not necessary for its location, site preparation and total animal handling time for routine venipuncture are minimal. Blood may be collected from immature and adult male and female animals, and the technique is easily taught to new technicians with minimal danger of injury to the animal.     

Long-Term Catheterization of the Intestinal Lymph Trunk and Collection of Lymph in Neonatal Pigs

Catheterization of the intestinal lymph trunk in neonatal pigs is a technique allowing for the long-term collection of large quantities of intestinal (central) efferent lymph. Importantly, the collection of central lymph from the intestine enables researchers to study both the mechanisms and lipid constitutes associated with lipid metabolism, intestinal inflammation and cancer metastasis, as well as cells involved in immune function and immunosurveillance. A ventral mid-line surgical approach permits excellent surgical exposure to the cranial abdomen and relatively easy access to the intestinal lymph trunk vessel that lies near the pancreas and the right ventral segment of the portal vein underneath the visceral aspect of the right liver lobe. The vessel is meticulously dissected and released from the surrounding fascia and then dilated with sutures allowing for insertion and subsequent securing of the catheter into the vessel. The catheter is exteriorized and approximately 1 L/24 hr of lymph is collected over a 7 day period. While this technique enables the collection of large quantities of central lymph over an extended period of time, the success depends on careful surgical dissection, tissue handling and close attention to proper surgical technique. This is particularly important with surgeries in young animals as the lymph vessels can easily tear, potentially leading to surgical and experimental failure. The video demonstrates an excellent surgical technique for the collection of intestinal lymph.     

一项小鼠采血新技术——颌下静脉丛采血法

目的介绍小鼠颌下静脉丛采血方法。方法选用2月龄昆明小鼠,固定小鼠后,将采血注射针头刺入颌下静脉丛血管取血。结果单人操作约1 min内可完成小鼠颌下静脉丛采血,采血量达到0.3-0.5 mL。结论此方法无需麻醉、创伤小、采血量大并可重复采血,是一种简便、安全、快速、采血量多的采血方法。     

一雄性灰鹤胃的血液供应

用血管铸型法对一只因伤致死的雄性灰鹤胃的血供进行铸型观察,结果显示,灰鹤的胃动脉均由腹腔动脉分出,腺胃由腺胃背侧动脉和腺胃腹侧动脉供应营养,肌胃由胃左动脉、胃右动脉和肌胃背侧动脉供应营养。腺胃的静脉有腺胃腹侧静脉、胃凹腹侧静脉和腺胃背侧静脉,分别经左（腺胃腹侧静脉和胃凹腹侧静脉）、右（腺胃背侧静脉）肝门静脉回流;肌胃的静脉有胃左静脉、胃右静脉和胃背侧静脉,分别经左（胃左静脉）、右（胃右静脉和肌胃背侧静脉）肝门静脉回流。此外本文将灰鹤胃的血供与其它动物的进行了比较。     

Skeletal age determination based on the os pubis: A comparison of the Acsádi-Nemeskéri and Suchey-Brooks methods

After reviewing various systems of age determination based on analysis of the pubic bone, the discussion concentrates on the collection and preparation of an extensive autopsy sample (n=1225) of pubic bones from modern individuals with legal documentation of age at death (death and/or birth certificates). TheSuchey-Brooks method derived from this sample is described. TheAcsádi-Nemeskéri system is evaluated in terms of the documented collection and it is seen that their five stage method focuses only on the early and late morphological changes. The intermediate stages, in which the ventral rampart is in process of completion, are not described. Their suggested age ranges do not correspond with the documented modern sample. Based on these limitations of theAcsádi-Nemeskéri method, applications of theSuchey-Brooks system are discussed.     

The effect of different sample collection methods on rabbit blood parameters

Nowadays great deal of research is physiological field is conducted on experimental animals and there is a lot of criticism from the wide public on methods used. Therefore, recently there is a lot of effort focused on the welfare of the animals. Main aim of this study is to determine the effect of experimental sample collection method on the selected parameters of stress. In the experiment two sample collections of rabbit blood from marginal ear vein were realized – first using standard method with one person fixing the animal and other collecting the blood using gently fixating the animal. In the second groups experimental method of inserting the experimental animal into a sack and further collection in dark was realized. During the experiment the levels of cortisol – main stress indicator in organism and other health parameters of animals including mineral profile and haematological parameters were observed. Our results show no significant changes in levels of cortisol but also a decreasing tendency in the sample from the second (dark) collection. Haematological parameters were generally in the reference values and any significant changes except levels of lymphocytes and percent of lymphocytes which shown significant increase in the second collection period were found. Also the levels of mean corpuscular haemoglobin and percent of neutrophils unveiled a significant decrease in values. Values of mineral profile parameters have indicated no significant changes except the levels of phosphorus. Based on the result we can state that the experimental sample collection has no effect on blood parameters of the animals but we spectated a statistically insignificant decrease in the levels of cortisol which can suggest that the dark collection is possibly less stressful to the animals.     

Blood collection from the facial (maxillary)/musculo-cutaneous vein in true frogs (family Ranidae)

Collection of blood from amphibians, as in other classes of vertebrate animals, is essential to evaluate parameters of health, diagnose hemoparasitism, identify viral and bacterial pathogens, and measure antibodies. Various methods of blood collection have been described for amphibians. Most can be cumbersome (venipucture of femoral vein, ventral abdominal vein or lingual venus plexus) or result in pain or deleterious health consequences (cardiac puncture and toe-clipping). We describe an easy and practical technique to collect blood from frogs and toads that can be used in multiple species and is minimally invasive. The technique consists of puncturing either the facial or, less commonly, the musculo-cutaneous vein and collecting the blood with a capillary tube. These veins run dorsal and parallel to the maxillary bone and can be accessed by quick insertion and withdrawal of a needle through the skin between the upper jawline and the rostral or caudal side of the tympanum. The needle should be of 27 or 30 gauge for anurans weighing more or less than 25 g, respectively. Although the technique has been used by some amphibian researchers for years, it is little known by others and has never been fully described in a peer-reviewed publication.     

Vascularization of the telencephalic choroid plexus of a ganoid fish [Acipenser ruthenus (L.)

The vascularization of the telencephalic choroid plexus of the sterlet Acipenser ruthenus, a ganoid fish, was examined by vascular corrosion casting and by light and transmission electron microscopy. The arterial supply is from the dorsal mesencephalic artery via: 1) the ventral choroidal arteries (left and right); 2) the dorsal choroidal arteries (left and right); 3) the caudal choroidal arteries (left and right); 4) the ventral arteries of the dorsal sac; and, from the olfactory arteries, via 5) the rostral choroidal arteries. The venous drainage is mainly through a single main choroidal vein that can take various courses either directly to the anterior cardinal vein or via the middle cerebral vein to the anterior cardinal vein. To a lesser extent, the plexus is drained via the lateral telencephalic veins and the ventral vein of the dorsal sac to the middle cerebral vein. By angioarchitecture and form, the plexus can be subdivided into five distinct parts: the surface network, the median folds, the large lateral folds, the small lateral folds, and the area common to the bottom of the dorsal sac and the telencephalic plexus. Diameters of terminal vessels as measured from vascular corrosion casts and from paraplast, semithin, and ultrathin sections were never less than 10 micron. It is suggested that the different areas in one plexus may have different functions with respect to secretion and absorption of cerebrospinal fluid.     

Acute effects of unilateral ovariectomy in the baboonPapio cynocephalus

The purpose of this study was to determine if steroids secreted by one ovary affected the steroid secretion of the other ovary by direct transportation of the steroids via uterine blood vessels. Either two or three baboons were scheduled for ovariectomy on the day of ovulation and on alternate days from 1–15 days before the expected day of ovulation. Two days before the scheduled ovariectomy, utero-ovarian vein blood from both sides was collected by the use of a laparoscope. Measurement of estradiol (E₂) was carried out in these samples. The ovary with a higher concentration of E₂ was designated the dominant side. At the time of ovariectomy utero-ovarian vein and uterine vein blood from the two sides was again collected. After removal of the dominant side ovary another sample of utero-ovarian and uterine vein blood was collected. The interval between removal of one ovary and blood collection from the contralateral side ranged from 2–15 min. Steroids E₂, progesterone (P), testosterone (T), and androstenedione (A) were measured in the blood plasma. Of the 21 baboons 12, 12, 11, and 10 baboons showed an increase in E₂, P, T, and A values, respectively, on the contralateral side after unilateral ovariectomy. The time elapsed between pre-ovariectomy blood collection and post-ovariectomy blood collection as well as the day of the follicular phase, when these samples were collected had no effect on the increases and decreases on the contralateral side. Statistical analysis, however, showed that the change in utero-ovarian vein or uterine vein hormone levels on the contralateral side after removal of one ovary was not significant for any of the four hormones E₂, P, T, and A. Thus there is no evidence to demonstrate cross circulation of steroids from one ovary to the other via direct vascular channels. This research was supported by NIH grant HD15300 toA. A. Shaikh.     

Intermittent sampling of portal venous blood and bile from guinea pigs

A technique is described for intermittent collection of portal venous blood from guinea pigs through a catheter advanced from an ileal tributary of the cranio-mesenteric vein into the portal vein and for the collection of bile from a catheter in the gallbladder after ligature obstruction of the common bile duct.     

The bronchial tree and blood vessels of the Japanese monkey lung

The author injected various colored celluloid solutions into the bronchial tree and blood vessels of the lungs of five adult Japanese monkeys (Macaca fuscata) in order to prepare cast specimens. These specimens were investigated from the comparative anatomical viewpoint to determine whether the bronchial ramification theory of the mammalian lung (Nakakuki, 1975, 1980) can be applied to the Japanese monkey lung or not. The bronchioles are arranged stereotaxically like those of other mammalian lungs. The four bronchiole systems, dorsal, ventral, medial, and lateral, arise from both bronchi, respectively, although some bronchioles are lacking. In the right lung, the bronchioles form the upper, middle, accessory, and lower lobes, while in the left lung, the upper and accessory lobes are lacking and bi-lobed middle and lower lobes are formed. In the right lung, the upper lobe is formed by the first branch of the dorsal bronchiole system. The middle lobe is the first branch of the lateral bronchiole system. The accessory lobe is the first branch of the ventral bronchiole system. The lower lobe is formed by the remaining bronchioles of the four bronchiole systems. In the left lung, the middle lobe is formed by the first branch of the lateral bronchiole system. The lower lobe is formed by the remaining bronchioles. Thus, the bronchial ramification theory of the mammalian lung applied well to the Japanese monkey lung. The right pulmonary artery runs across the ventral side of the right upper lobe bronchiole. It then runs along the dorso-lateral side of the right bronchus between the dorsal bronchiole system and the lateral bronchiole system. On its way, it gives off branches of the pulmonary artery which run along the dorsal or lateral side of each bronchiole except in the ventral bronchiole system. In the ventral bronchiole system, the branches run along the ventral side of the bronchioles. The distributions of the pulmonary artery in the left lung are the same as those in the right lung. The pulmonary veins do not always run along the bronchioles. Most of them run on the medial or ventral side of the bronchioles. Some of them run between the pulmonary segments. In the right lung, these pulmonary veins finally form the right upper lobe vein, right middle lobe vein and the right lower lobe pulmonary venous trunk before entering the left atrium. However, the right accessory lobe vein runs on the dorsal side of the bronchiole and pours into the right lower lobe pulmonary venous trunk. In four cases out of the five examples, part of the right lower lobe veins pour into the right middle lobe vein, while the others enter the right lower lobe pulmonary venous trunk. In the left lung, the branches of the pulmonary veins finally form the left middle lobe vein and the left lower lobe pulmonary venous trunk.     

Orbital venous anatomy of the rat

Ten rats were embalmed, the veins of the head latex-injected, and the heads were dissected. Five rats were used to prepare corrosion casts of the venous structures of the head. It was found that the rat has an orbital venous plexus rather than an orbital venous sinus as seen in the mouse and hamster. The orbital venous plexus was formed by the external dorsal ophthalmic vein, the external ventral ophthalmic vein and numerous anastomoses between these veins. Of major interest was a large anastomotic vein located in the caudaldorsal area of the orbit. The anastomotic vein joined the orbital venous plexus and the superficial temporal vein.     

A simple method for intravenous injection and blood collection in the chinchilla (Chinchilla laniger)

A simple method is outlined for intravenous injection and blood collection from a peripheral vein in the chinchilla. Seven peripheral vein sites were successfully venipunctured in unanaesthetized chinchillas: the femoral, cephalic, auricular, saphenous, dorsalis penis, lateral abdominal and tail veins. The femoral and cephalic veins were found to be the best sites for injection and blood collection.     

An Angiocardiographic Analysis of the Central Circulation in the Air Breathing Teleost Channa argus

The unique anatomy of the double ventral aorta outflow system in the air breathing teleost Channa argus (Ophiocephalus) showing an anterior and posterior ventral aorta is described. The marked trabeculation of the ventricle and bulbus arteriosus and the arrangement of central veins are used as a basis for the hypothesis that Channa may selectively channel the well oxygenated blood draining the air breathing organs via the anterior cardinal vein to the posterior ventral aorta, which forms the systemic arterial circulation. An angiocardiographic technique was used to test this hypothesis, as well as to delineate the functional role of the heart chambers in the cardiac cycle. No reflux of contrast to the sinus venosus during atrial filling and no ventricular filling before atrial contraction were apparent, which makes the atrium the main determinant of the ventricular end-diastolic volume. Ventricular contraction left a small or no residual volume. The ventricular ejectate was initially nearly completely absorbed by the very elastic bulbus arteriosus, acting as a pressure chamber (Windkessel) stabilizing and prolonging ventral aortic blood flow. Contrast medium was not selectively passed from the anterior cardinal vein to the posterior ventral aorta. However, the diameter of this vessel and its density of contrast were greater than in the anterior aorta, suggesting a preference for a greater blood flow from the air breathing organ through the heart to the posterior aorta.     

Impact of blood sampling technique on blood quality and animal welfare in haemophilic mice

Blood collection in mice can be a challenge, in particular for samples used for coagulation analysis as initiation of coagulation during the procedures can influence the results. Blood collection from the retrobulbar venous plexus is commonly used but the method remains controversial. Several alternatives exist but not all are applicable to mice with a compromised coagulation system because of subsequently excessive bleeding. We therefore wanted to explore whether blood collection by puncture of the submandibular vein could replace blood collected from the retrobulbar venous plexus during pharmacokinetic and pharmacodynamic studies in mice lacking coagulation factor VIII (FVIII). The plasma concentrations of recombinant activated factor VII were independent of the blood collection method in a pharmacokinetic study. The same applied to the thromboelastographic profile of mice with normal coagulation in a pharmacodynamic study. However, excessive haemorrhages were observed in all FVIII knockout mice after a single puncture of the submandibular vein and 60% of the mice were euthanized 2-4 h after the blood collection. In contrast, no or only slight haemorrhage was observed in animals subjected to blood collection from the retrobulbar venous plexus. No signs of distress determined by blood glucose level or clinical abnormalities of the eye were observed after puncture of the retrobulbar venous plexus. In conclusion, blood collected by puncture of the submandibular vein and retrobulbar venous plexus has a quality which allows it to be used in coagulation assays. However, because of excessive bleedings, puncture of the submandibular vein is not recommended in mice lacking FVIII.     

Distribution of the pulmonary artery and vein in the chimpanzee lung

Lungs of two chimpanzees (Pan troglodytes) were examined. The right pulmonary artery runs across the ventral side of the right upper lobe bronchiole and, then across the dorsal side of the right middle lobe bronchiole. Thereafter, it runs between the dorsal bronchiole system and the lateral bronchiole system, along the right bronchus. During its course, it gives off arterial branches which run along each bronchiole. The left pulmonary artery runs across the dorsal side of the left middle lobe bronchiole and then between the dorsal bronchiole system and the lateral bronchiole system. The branches of the pulmonary artery run mainly along the dorsal or lateral side of the bronchiole. The pulmonary veins run mainly along the ventral or medial side of the bronchioles, and between them. Finally, they enter the left atrium with four large veins, i.e. the common trunk of the right upper lobe vein and the right middle lobe vein, right lower lobe pulmonary venous trunk, left middle lobe vein, and left lower lobe pulmonary venous trunk.     

Interrelationships Between Arteries,Veins and Lymphatics in the Head Region of the Eel,Anguilla anguilla L.

Vascular casting and dissection of fresh specimens had been used to investigate the arrangement of vessels before and after the gills in the head region of the eel. Arterial and venous morphology was found to be as reported in previous works, but the presence in the eel of a venous system that does not confom to the generalised teleost plan necessitated the use of a non-standard nomenclature. The gills are the site of the connection of the arterial system with a second vascular system and it is suggested that this system should be termed the veno-lymphatic system. The veno-lymphatic system connects dorsally to the systemic lymphatic system and so to the internal jugular vein. Ventrally the veno-lymphatic vessels from the first three gill arches are collected into a connective tissue sheath around the ventral aorta. The sheath is connected to a veno-lymphatic sinus posterior to it which also collects the veno-lymphatic of the fourth gill arch. This sinus then drains into the external jugular vein which at this point is the fusion of the left and right branches. These later separate and each branch contains a valve preventing flow towards the ventral aortic sheath. It is proposed that because of the form of this ventral route for veno-lymphatic drainage, and the ease and completeness of filling of this route compared with the dorsal route, that the ventral veno-lymphatic system is probably the primary route of drainage of veno-lymphatic outflow from the gills.     

Development of the vasculature of the pectoral fin in the Australian lungfish, Neoceratodus forsteri

The development of the vasculature of the pectoral fin in the Australian lungfish, Neoceratodus forsteri, was studied by the dye-injection method. Only a single primitive subclavian artery appears from the dorsal aorta for the fin anlage, and it passes laterally through the postaxial region of the structure. The venous channel draining into the posterior cardinal vein is located in the preaxial region medially. As development proceeds, the arteriovenous arrangement in the pectoral fin anlage changes as follows: 1) one artery and one venous plexus, 2) two arteries and one vein, 3) three arteries and one vein, 4) four arteries and one vein, 5) three arteries and two veins, and 6) two arteries (radial and ulnar) and three veins (radial, ulnar, and ulnar marginal). The fin anlage through embryonic first rotation has gradually changed its postaxial margin to face dorsally and its preaxial margin to face ventrally. The second rotation causes the original preaxial margin to become dorsal and the original postaxial margin to become ventral. As a result, the radial and ulnar arteries are observed in the dorsal and ventral regions, respectively, in the medial side of the fin instead of in the lateral side as seen in the previous stage.     

环颈雉胃的血供

用血管铸型法和大体解剖学方法对环颈雉胃动脉的起源、分布及胃静脉的回流情况进行了解剖学研究。结果表明,环颈雉的胃动脉均由腹腔动脉分出;腺胃由腺胃背侧动脉和腺胃腹侧动脉营养,腺胃背侧动脉直接起自腹腔动态的左侧,腺胃腹侧动脉起自腹腔动脉左支。腺胃血液的静脉有腺胃前静脉和腺胃后静脉,分别汇入后腔静脉和左肝门静脉。肌胃由肌胃左动脉、肌胃右动脉和肌胃背侧动脉营养,肌胃左动脉起自腹腔动脉的左支;肌胃右动脉起自腹腔动脉的右支;肌胃背侧动脉从腺胃背动脉分支而来。回流肌胃血液的静脉有胃右静脉、胃左静脉和胃腹侧静脉;胃右静脉汇入右肝门静脉,胃左静脉和胃腹侧静脉汇入左肝门静脉。另外腺胃和肌胃的表面缺乏主干动脉间的吻合。