Background
The formation of CSF has been studied extensively [
1] and the physical location at which it is formed within the ventricular system (the choroid plexus) has been well established. In contrast, while CSF absorption parameters have been investigated in many species, the mechanism and location of the transport sites is far from clear. It is assumed that projections of the arachnoid membrane into the cranial venous sinuses facilitate CSF removal however, there is very little convincing quantitative evidence to support a role for arachnoid villi and granulations in this process. Recent experiments suggest that the movement of CSF directly into the cranial venous system may only occur at high pressures suggesting that the arachnoid projections may have an accessory function rather than representing the primary locations at which CSF is absorbed [
2,
3].
The experimental evidence would seem to favour the view that a significant portion of CSF is removed from the subarachnoid space by nasal lymphatic vessels. This conclusion is based on experiments that span over 100 years of investigation [reviewed in [
4]] with the most extensive analysis of CSF transport having been carried out more recently in sheep [
2,
3,
5‐
17]. CSF convects through the cribriform plate into lymphatic vessels located in the submucosa associated with the olfactory and respiratory epithelium. The lymph within the ethmoidal lymphatics appears to be continuous with CSF in the perineurial spaces associated with the olfactory nerves. Multiple lymphatic ducts form a collar around the emerging nerve roots, which facilitates direct connection between CSF and lymph in the olfactory submucosa [
18]. An extensive complex of lymphatic vessels in the ethmoid turbinal system conveys CSF through a variety of lymph nodes in the head and neck region to the cervical lymphatics that in turn, convey the CSF to the venous system [
3].
There is also substantial data with various tracers and dyes that this lymphatic CSF transport pathway is a characteristic feature of many mammals [
4]. However, there is still some uncertainty regarding the applicability of animal concepts to CSF transport in man. It has been argued that the larger brain, lack of sophisticated olfactory mechanisms and bipedal versus quadrapedal location make CSF transport in humans fundamentally different than that in animals.
There is no easy way to address the issue of lymphatic CSF transport in humans but recent experience visualizing CSF-lymph connections with Microfil, suggested that it may be possible to examine lymphatic CSF transport pathways in any species
post-mortem. Microfil is a coloured, liquid silicone rubber compound which, when combined with a catalytic curing agent, polymerizes within 20 minutes. This agent facilitates the generation of 3 dimensional images of the spaces into which it has been injected. In a previous report, we infused Microfil into the subarachnoid compartment of sheep and noted that it was carried through the cribriform plate into an extensive network of lymphatic vessels in the nasal submucosa of this species [
2,
3,
17,
18]. Drawing on this experience, the main objective of the studies reported here was to examine potential CSF-nasal lymph pathways in a variety of species including human and non-human primates. The results of this investigation support the view that lymphatics play an important role in CSF transport in all mammalian species.
Methods
Animals
All animal experiments were approved by the ethics committee at Sunnybrook and Women's College Health Sciences Centre and conformed to the guidelines set by the Canadian Council on Animal Care and the Animals for Research Act of Ontario. Studies in the sheep, mouse, rat, rabbit and pig were performed at Sunnybrook and Women's College Health Sciences Centre. Studies on the Barbados green monkey were performed at the Barbados Primate Research Centre and Wildlife Reserve. Investigation of human specimens was approved by the Chief Coroner and the General Inspector of Anatomy for Ontario. These studies were conducted at the University of Toronto, Department of Surgery, Division of Anatomy.
Experimental Objectives
The objective of these studies was to infuse a CSF tracer, Microfil (Flowtech, Mass), into the cranial subarachnoid space post-mortem to outline the pathways of CSF outflow. To accomplish this, the specimen was placed in sternal recumbancy with the head fixed in position. A laminectomy was performed on the upper regions of the spinal cord (generally between C1-C2) and the cisterna magna was cannulated with an angiocatheter or a silastic tube of appropriate size. A ligature was placed around the spinal cord and tightened to compress the spinal cord and meninges [
13]. This ligature served two purposes. First, as we were interested in cranial absorption pathways, the amount of Microfil infused was less since this agent was prevented from passing into the spinal subarachnoid compartment during injection. Second, our experience suggested that infusion pressures effective in filling the pathways of interest were more easily achieved with the spinal CSF space negated.
With the exception of studies in the mice, all experiments were performed by infusing Microfil manually using a syringe. We did not routinely monitor infusion pressures post-mortem. However, in several of our initial studies in sheep, we measured infusion pressures between 200 and 300 cm H2O. Mice on the other hand appeared to be very fragile and injection by hand was problematic. In this species, we found that Microfil filling was more successful if this agent was introduced into the CSF compartment using a free-flow pressure system and reservoir as described below.
The best results were obtained using a Microfil preparation that was more dilute than that recommended in the product literature. To achieve this, 3 ml of diluent was used for every 1 ml of yellow Microfil® (MV-122) and the material catalyzed with 10% (of total volume) of MV Curing Agent. In several sheep, blue Microfil (prepared as recommended in the instruction manual) was introduced into the vasculature at the same time that yellow Microfil was injected into the CSF compartment. The carotid arteries were catheterized and 20 ml of blue Microfil® (MV-120) was infused into both arteries simultaneously. More specific details pertaining to each species is outlined below.
Mice
Randomly bred, wild-type C57/Bl mice (n = 21, 16–19 gm; ~4–5 weeks old) were used for this investigation. They were fed lab rat chow (LabDiet 5001) until sacrifice. At the start of the preparation, the mice were euthanized. A laminectomy was performed at the C7 cervical-thoracic level of the vertebral column. Microfil was infused into the cranial subarachnoid space by one of two methods. In some preparations, Microfil was infused into the cranial subarachnoid space over a 5–10 minute interval through manual injection into an angiocatheter. In other experiments, the Microfil was administered using a free-flow pressure system with a reservoir filled with saline regulating the rate of flow into the cisterna magna. To achieve this, the three ports of a 3-way stopcock were attached to (a) a syringe containing Microfil, (b) a cannula attached to an angiocatheter inserted into the subarachnoid space, and (c) a cannula filled with saline hung vertically from a pole. The reservoir height was adjusted such that the saline solution exerted a pressure of approximately 100 cm H20. Microfil was injected via the syringe until the agent reached the hub of the angiocatheter. At this point, the stopcock was adjusted to allow the column of PBS to exert a pressure on the Microfil, which pushed the contrast agent into the subarachnoid space.
Rats
Randomly bred, Fischer 344 rats (n = 6, ~300 gm; 11–15 weeks old) were used for this investigation. They were fed lab rat chow (LabDiet 5001) until sacrifice. The rats were anaesthetized initially by placement in an induction chamber in which 5% halothane was administered for 2 minutes. Immediately after anesthesia, the rats were euthanized. A laminectomy was performed at the C7 cervical-thoracic level of the vertebral column. Microfil was infused into the cranial subarachnoid space over 5–10 minutes.
Rabbits
Randomly bred, New Zealand white rabbits (n = 2, 3 and 4 kg; ~18 weeks old) were used for this investigation. They were fed rabbit chow (LabDiet 5321) until sacrifice. The rabbits were initially anesthetized with an intramuscular injection of Ketamine (50 mg/kg) and Rompun (5 mg/kg). Prior to surgery, the rabbits were euthanized. A laminectomy was performed at the C7 cervical-thoracic level of the vertebral column. Microfil was infused into the cranial subarachnoid space over a 5–10 minute period.
Sheep
Randomly bred sheep (n = 29; 2.6–35 kg) including newborns (2–7 days old) and adult animals (6–8 months old) were used for this investigation. The neonatal lambs were bottle-fed formula (Lamb Replacement, Grober Inc. Cambridge, Ontario) until surgery. The lambs were anaesthetized initially by mask administration of incremental concentrations of halothane from 0.5 to 3%. The adult sheep were anesthetized initially by intravenous infusion of 2.5% sodium Pentothal solution. Subsequently, 1–3% halothane was delivered through an endotracheal tube via an A.D.S.1000 or Narkomed 2 respirator for surgical maintenance. In this species, a laminectomy was performed at the C1-C2 level under anesthesia followed by sacrifice. Microfil was infused into the cranial subarachnoid space over 10–15 minutes. In some animals, blue Microfil (prepared as recommended in the instruction manual) was introduced into the vasculature at the same time that yellow Microfil was injected into the CSF compartment. The carotid arteries were catheterized and 20 ml of blue Microfil® (MV-120) was infused into both arteries simultaneously.
Pigs
Randomly bred, Yorkshire pigs (n = 5, 20–25 kg; 8–9 weeks old) were used for this investigation. They were fed pellets (LabDiet Laboratory Animal Diet) until sacrifice. The pigs were anesthetized initially with an intramuscular injection of Ketamine (30 mg/kg) and Atropine (0.04 mg/kg). Surgical anesthesia was induced and maintained by 2–5% halothane delivered through an endotracheal tube via a Narkomed 2 respirator. Prior to surgery, the pigs were euthanized. A laminectomy was performed at the C1-C2 level and Microfil was infused into the cranial subarachnoid space over a 10–15 minute period.
Monkeys
Randomly bred, Barbados green monkeys (Cercopithecus aethiops sabeus) (n = 6, 4.0–5.6 kg; ~6 years old) were used for this investigation. They were fed twice daily various natural foods until sacrifice. At the start of the preparation, the monkeys were anaesthetized with Xylazine/Ketamine (100 mg/kg) injection. Subsequently, the monkeys were euthanized. A laminectomy between C7 and T1 was performed and Microfil was infused into the cranial subarachnoid space over a 5–10 minute period.
Humans
Three recently deceased cadaveric preparations were examined (3 females, 77, 80 and 90 yrs old). Access to the cadaveric material was permitted between 6 and 7 hours post mortem. A laminectomy between C7 and T1 was performed and Microfil was infused into the cranial subarachnoid space.
Analysis of tissues
Following injection with Microfil, the heads of mice, rats, rabbits, sheep and pigs were stored at 4°C overnight. The next day, the heads were skinned, sectioned in a sagittal orientation and fixed in 10% formalin. In the monkey studies, the Microfil was allowed to set for 2 hours after injection followed by sectioning and fixation with formalin (2–3 weeks) and 70% alcohol (immediately before shipment to Canada). After Microfil infusion in humans, the heads were placed in a freezer for several days (-18°C) after which they were sectioned and fixed with Kaiserling's solution for at least 5 days before dissection.
Sectioning of the fixed tissues was made in several orientations including coronal cuts anterior and posterior to the cribriform plate and/or sagittal sections. The various tissues were dissected as appropriate under a dissecting microscope (Leica M651, Wild Leizt; EMZ-TR, Meiji Techno; Fisher Stereomaster) and images were captured on a Nikon digital camera (Coolpix 995). All images presented in this report are in the midsagittal plane from the cut surfaces of the heads.
Discussion
Nasal lymphatic vessels have been implicated in CSF transport for many years. However, the concept has not received mainstream acceptance for several reasons.
First, the data supporting lymphatic function has been based entirely on animal studies especially the sheep. However, histological and radiological evidence indicate that CSF-lymph connections exist in other species including rats [
8,
19‐
24], mice [
25], rabbits [
26‐
28], cats [
20,
29,
30], dogs [
20,
30], guinea pigs [
31], and non-human primates [
30,
32]. In the latter case, injection of radioactive albumin into the CSF compartment of monkeys led to elevated concentrations of tracer in the cervical lymph nodes [
32].
Circumstantial evidence also suggests that similar CSF-lymphatic connections exist in humans as well [
22,
33‐
36]. For example, Indian ink administered into the CSF in human autopsy material [
35] was observed to fill the perineurial spaces around the olfactory nerve branches and was found in the nasal submucosal tissue. Similarly, in an individual with subarachnoid hemorrhage, red blood cells were observed around the olfactory nerves and within the nasal mucosa. However, until now, direct evidence that the CSF and lymph compartments were linked in human and non-human primates was lacking.
The Microfil images presented in this report demonstrate that the passage of CSF along the olfactory nerves into lymphatics is a characteristic feature of several mammalian species. The Microfil distribution patterns from the mouse to the human were remarkably similar. It must be acknowledged that we had limited access to human material and that studies with the cadaveric material are ongoing. However, the fact that Microfil was observed external to the cranium in the nasal submucosa adjacent to the cribriform plate in both human and Barbados green monkey specimens supports the view that CSF absorption in primates is not significantly different (at least qualitatively) from that in other mammalian species.
In a previous study, we injected yellow Microfil into the subarachnoid space and blue Microfil into the carotid arteries [
18]. This protocol permitted the separation of the blood vessels from lymphatics without the use of promiscuous molecular markers. Indeed, the larger Microfil-filled lymphatic vessels demonstrated the classical 'lymphangion' structure with constrictions of the vessels where the valves were positioned (example in Fig
5C). The vessels could be traced in some instances to prenodal ducts that converged on various lymph nodes [
18]. In the study reported here, we have included examples of this in sheep and mice (Figure
5C,5D).
Studies with Microfil provide valuable information on 'potential' CSF transport routes but one must be cautious in applying post-mortem observations to physiological processes. However, in sheep there is considerable quantitative data that supports the concept that the cribriform-olfactory nerve-lymphatic pathway contributes significantly to volumetric CSF absorption [
2,
3,
5‐
9,
11,
13‐
16]. Given that the Microfil distribution patterns in sheep, pigs, rabbits, rats, mice, Barbados green monkeys and humans appear remarkably similar, it would seem likely that this pathway is important for CSF clearance in each of these species.
Another reason for the skepticism regarding the role of lymphatics in CSF transport is the generally held view that arachnoid projections function in this role. However, the quantitative evidence supporting a role for arachnoid projections is very limited and unconvincing [
37‐
39]. It must be acknowledged that we observed Microfil within a variety of veins external to the cranium and in the dural sinuses. With regards to the former, Microfil entry was due (at least in part) to passage of the contrast agent through the dura at the base of the brain into the cavernous sinus. The Microfil appeared to push into this venous system and fill several veins. Whether this observation has any physiological relevance is unknown.
The route by which Microfil gains entry into the dural venous sinuses is unknown but is currently under investigation. However, the concept of direct CSF transport into the superior sagittal sinus continues to be problematic. We used several experimental approaches to assess this issue in previous studies in sheep. The most informative technique was to employ the classical approach of Mann to look for enrichment of a radioactive CSF tracer in the superior sagittal sinus compared to a peripheral vein [
40]. The Mann group observed that the concentration of soluble and particulate tracer was considerably greater in the sinus blood than in the peripheral circulation (inulin concentrations were up to 30 times greater). However, the peak CSF pressures achieved during bolus infusions were greater than 80 cm H
2O, a level of pressure that is clearly pathological. Other groups have failed to observe enrichment of a CSF tracer in the superior sagittal sinus of the rabbit, cat and monkey when the intracranial pressures achieved in the experiments simulated physiological conditions more realistically [
32,
41,
42].
In our investigations in adult sheep, at a CSF-superior sagittal sinus pressure gradient of around 10 cm H
2O (normal gradient ~5 cm H
2O) no enrichment was observed. When the gradient favouring absorption was greater than 20 cm H
2O, a modest enrichment of tracer was noted [
3].
A similar result was obtained with tracer enrichment experiments in newborn lambs. The latter result was surprising. Adult sheep have abundant arachnoid projections in the superior sagittal sinus which are visible when stained with Evans blue dye but, in the neonatal lamb, arachnoid projections are few or absent [
2]. Therefore, tracer transport into the superior sagittal sinus could not be correlated with the presence or absence of arachnoid projections although some transport directly into the cranial venous system seemed to occur.
In our studies the maximum enrichment of CSF tracer in the superior sagittal sinus was observed only within the first few minutes after increasing intracranial pressure [
3]. Within a short time, the tracer concentrations in the sagittal sinus and peripheral venous blood were equal. This suggested the possibility that the tracer enrichment method outlined above has the potential to underestimate the role of arachnoid projections since vigorous tracer transport to peripheral veins by some other mechanism could cancel out any perceived tracer enrichment in the cranial venous sinuses. Projections of the arachnoid membrane into the veins at the base of the brain have been described but at this time, there is no evidence that these structures play a role in CSF transport. The most obvious contributor to the peripheral venous tracer would be the lymphatic circulation.
To determine if the lack of CSF tracer enrichment in the superior sagittal sinus was due to lymphatic transport into peripheral veins, we created what we thought would be the conditions most favourable to measure clearance via the arachnoid granulations. We sealed the cribriform plate and prevented CSF transport into the spinal subarachnoid compartment thus negating much of the lymphatic transport capacity. Nonetheless, even under these conditions when the CSF-superior sagittal sinus pressure gradient was raised to 20 cm H2O (~4 fold higher than normal), no enrichment was observed. At pressure gradients greater than this level, the concentration of the tracer was significantly higher than in the peripheral circulation. Therefore, the lack of enrichment of the CSF tracer in the superior sagittal sinus at normal physiological intracranial pressures does not appear to be due to downstream lymphatic transport of the CSF tracer. Contrary to the 'classical' view, direct transport of CSF into cranial veins (whether this occurs through arachnoid projections we cannot determine unequivocally) may represent an auxiliary system that is recruited when intracranial pressures are high or when other transport pathways are compromised.
In summary, we have never been able to obtain persuasive evidence that direct CSF transport into the venous system is a physiological reality. In contrast, the qualitative and quantitative support for nasal lymphatic role in CSF absorption is gaining momentum.
Author's Contributions
MJ: conceived of the study, and participated in its design and coordination.
AZ: developed the application of the Microfil method to the analysis of CSF transport pathways, participated in all experiments, created an image catalogue and helped in the preparation of the manuscript.
CP: aided in the experiments in human, sheep, rats and mice and helped in the preparation of the manuscript
GS: performed the studies in rats and mice
DA: in conjunction with AZ performed the studies in humans and monkeys and assisted in all experiments.
All authors read and approved the final manuscript.
Competing Interests
The author(s) declare that they have no competing interests.