- Open Access
Evidence for reduced lymphatic CSF absorption in the H-Tx rat hydrocephalus model
© Rammling et al; licensee BioMed Central Ltd. 2008
- Received: 05 July 2008
- Accepted: 16 October 2008
- Published: 16 October 2008
There is mounting evidence that spinal fluid absorption takes place not only at the arachnoid villi, but also at several extracranial sites, which might serve as a reserve mechanism for, or be primarily involved in the absorption of CSF in hydrocephalus.
We compared the nasal lymphatic pathway in congenital Hydrocephalus-Texas (H-Tx) rats in unaffected and affected hydrocephalic (HC) siblings with that of control Sprague Dawley (SD) rat pups. The animals were examined after immediate post mortem injection of Evan's blue dye into the cisterna magna at 6 and 10 days of age. The specimens were evaluated for amount of dye penetration into the nasal passages.
We found more dye visualization in the olfactory regions of control SD (14/16 at P6, 14/16 at P10) and unaffected H-Tx (13/17 at P6, 13/16 at P10) compared with HC animals (0/14 at P6, 3/15 at P10). This difference was more pronounced at 10 days of age. The dye was not visualized in the cervical lymph nodes or venous channels in these acute experiments.
The results of this study suggest that nasal lymphatic cerebrospinal fluid absorption is reduced in the H-Tx rat hydrocephalus model.
- Subarachnoid Space
- Sprague Dawley
- Nasal Passage
- Cribriform Plate
Hydrocephalus is a lifelong condition of cerebrospinal fluid (CSF) imbalance, leading to seizures, neurological and cognitive dysfunction, or death if left untreated. The condition is not a single pathologic entity, nor is it a simple, well-defined disease process; rather, it encompasses a diverse group of clinical situations sharing a common feature of increased intracranial pressure (ICP) resulting from an imbalance of CSF secretion and absorption. A better understanding of these as yet undiagnosed mechanisms may offer therapeutic options for rebalancing CSF dynamics before fluid accumulation occurs.
We must reconsider the conventional wisdom that primary CSF absorption occurs through the arachnoid granulations, since there is limited evidence concerning fibrosis or anatomic obstruction at these sites in hydrocephalus [1–4]. Yet there is increasing evidence for communication between the CSF pathways and the extracranial lymphatic system, mostly by the nasal lymphatics or the optic nerve sheath into the facial venous system, elegantly described by Johnston et al to be functional in most mammals, including humans [5–9]. This group found that approximately 50% of CSF is cleared from the cranial compartment by the nasal lymphatic vessels, which play a major role in bulk flow of spinal fluid into the venous system. Other studies confirm that CSF drains along cranial nerves eventually into the lymphatic channels [10–13]. Accumulation of excessive spinal fluid, especially under increased pressure, could implicate a problem in these mechanisms. [14–19].
We hypothesize that obstruction of CSF flow via the cribriform plate into the facial lymphatic pathways is related to hydrocephalus in the Hydrocephalus-Texas (H-Tx) rat model. We investigated nasal lymphatic pathways in hydrocephalus by injecting Evan's blue dye into the cisterna magna of Sprague Dawley (SD) rats, unaffected H-Tx rats, and their affected hydrocephalic (HC) siblings at post natal days P6 and P10, and studied the amount of dye penetration in the nasal regions.
The H-Tx rat was initially identified in 1981 by Kohn, et al. , and a colony from animals originally from the University of Florida is maintained at our institution by brother-sister mating. Although the genetic cause of the H-Tx mutation is unknown, it is a widely recognized animal model that mirrors the human condition. Hydrocephalus occurs in approximately 20–40% of each litter, with obstruction of the aqueduct on day E18 [21, 22]. The ventricular system dilates rapidly, as evidenced by an enlarged, domed dorsal cranium evident by 1–2 days of age . Most hydrocephalic rats die at 4–5 weeks of age if not treated by shunting procedures, which confer a normal life span [23, 24].
Evan's blue dye penetration into olfactory turbinates of control and hydrocephalic rats.
Magnetic resonance imaging
Tracer injection and visualization
In order to compare experiments using anesthetized animals with those after CO2 euthanasia, initial experiments were performed using 10-day old pups (n = 18) anesthetized using pentobarbital (20 mg/kg, i p). Evan's blue dye (50 μL, 2% in PBS) was injected into the cisterna magna subarachnoid space. The animals were sacrificed after 20 min by an additional injection of pentobarbital (50 mg/kg).
Ninety four animals (47 at P6 and 47 at P10) were sacrificed by CO2 inhalation and underwent immediate post mortem injection (30 μL at P6, and 50 μL at P10) of 2% Evan's blue dye in PBS into the cisterna magna subarachnoid space.
After dye injection, pups were kept in head-dependent supine position at -20°C for 24 h prior to sectioning. Sections 1 mm thick were made by hand in coronal or sagittal planes on dry ice, and images at 40× magnification were obtained under a dissecting microscope (Zeiss, STEMI SV 11, Germany), and captured by a digital camera. These images were used to examine for dye penetration from the cribriform plate into the olfactory turbinates and nasal pathways. Alpha Imager 2200 software was used to quantify the amount of dye visualized in the nasal regions between the 3 groups of animals (Alpha Innotech Corp. CA). We arbitrarily assigned the average value of HC animals as reference (baseline of 1), and compared the SD and H-Tx groups against this value for relative dye intensity.
Eighteen animals at P10 were initially utilized for live injection of Evan's blue dye under pentobarbital sedation prior to sacrifice. Adequate visualization of dye within the olfactory turbinates was seen in the six SD and six unaffected H-Tx pups, but no visible dye was noted in the six affected HC animals.
The larger series with 47 pups at P6 and 47 at P10 was performed using post mortem injection after CO2 euthanasia. Evan's blue dye was visible within the nasal passages of 14/16 pups at P6 and P10 in the SD animals. Similarly, in the unaffected H-Tx group, dye was visualized in 13/17 of pups at P6 and 13/16 at P10. However, there was no dye visible in the olfactory turbinates of 14 HC animals at P6 and only 3/15 had visible dye in the olfactory regions at P10 (Table 1, Figure 2). The dye was not visualized in the cervical lymph nodes or venous channels in these acute experiments.
Relative fold increase in Evan's blue dye concentration into the olfactory turbinates of control rats compared to hydrocephalic rats.
Initial concepts of hydrocephalus pathophysiology were based on a limited understanding of CSF dynamics, alternative flow pathways, and the compensatory mechanisms involved. While ongoing fundamental studies explore the complex mechanisms of normal brain development, those involved in the molecular basis of hydrocephalus remain unexplained. Thus, medical management of this lifelong condition remains elusive, with few research efforts in this direction.
Anatomical and tracer studies have identified CSF flow in the subarachnoid spaces surrounding the olfactory nerves into the cribriform plate into a network of lymphatic ducts in the olfactory turbinates [25–27]. The fluid is then conveyed into progressively larger lymph channels and ultimately deposited into the venous system in the cervical region [16, 17, 28]. In rodents, these associations are not observed until four days after birth, when CSF production significantly increases. Timing of this occurrence perhaps suggests a pressure-dependent mechanism to open and maintain these CSF outflow channels .
Recent studies by Nagra, et al. identified decreased flow in the nasal passages of rats with acquired hydrocephalus by kaolin injection, where intraventricular injection of Evan's blue dye did not penetrate the subarachnoid spaces and was not visualized in the nasal passages . Scarring or obliteration of the arachnoid spaces near the olfactory region may contribute to the diminished flow via these pathways in this induced hydrocephalus model. Evan's blue dye was used for its ease of handling, and the ability to assess the anatomic CSF localization in the post mortem animals . Evan's blue dye in PBS was found to be very effective in delineating the pathways and appears to be as effective as dye linked to protein (Johnston, M, personal communication).
In our animals, dye penetration was limited in the nasal passages, despite adequate representation of dye within the subarachnoid spaces in the basal cisterns and surrounding the cribriform plate (Figure 3). We therefore postulate that CSF in the hydrocephalic animals had access to the cribriform plate and the nasal passage for egress, suggesting a primary obstruction at these sites. Studies to identify further delineate the anatomic sites of blockage are necessary.
Although these nasal pathways for CSF absorption are known to exist in several species, this is the first study to document their connection with congenital hydrocephalus. Since hydrocephalus is a multifactorial condition, perhaps diminished nasal lymphatic outflow tracts increase the propensity to develop the condition. There might be a triggering factor which cannot be overcome in a certain number of animals leading to increased susceptibility to a stimulus such as infection or subarachnoid hemorrhage.
In animal experiments, obstruction of the cribriform plate reduces CSF clearance and leads to increased ICP, but it is unclear if it is involved in hydrocephalus [8, 15, 30]. Ludemann, et al. studied the ultra structure of CSF outflow along the optic nerve and identified pore-like openings in a thin neurothelial layer extending into the lymphatics, which might respond to elevated CSF pressure . Similar mechanisms might play a role in increased intracranial pressure in mammals.
In H-Tx animals the hydrocephalus is associated with aqueductal stenosis at E18, and the condition progressively worsens until death at 5–6 weeks of age . However, the nasal pathways for CSF absorption develop at post natal day 4 in rats, which calls into question the possibility of a causal relationship between CSF drainage pathways and hydrocephalus . It is plausible that the nasal lymphatic pathway is an outflow track dependent on pressure-driven mechanisms for proper development and function. This submucosal CSF egress might serve as a compensatory mechanism that fails when most needed. We studied the H-Tx animals at 6 days of age and later dates to assess the possibility of secondary, pressure-driven recruitment of these pathways. Dye penetration was more pronounced in normal animals at P10, and it was better defined in deeper ethmoid sinus regions of the older animals, suggesting some recruitment of these pathways over time. Evan's blue was not visualized in the cervical lymph nodes in these animals.
The nasal passages may constitute another route for CSF absorption that can be recruited either temporarily or permanently at times of increased intracranial pressure (such as hydrocephalus). Drugs administered intranasally may gain access to the brain via axonal transport along the olfactory receptor cells extending through the cribriform plate to the olfactory bulb . We hypothesize that pore-like openings responsible for extracranial olfactory CSF drainage are obstructed in the affected (hydrocephalic) H-Tx animal, and they may be reopened using newer therapeutic measures.
Our data suggest that the nasal lymphatic drainage pathway of CSF absorption is present in normal SD and unaffected H-Tx rat pups at 6 and 10 days of age and diminished or absent in hydrocephalic rat pups. The nasal lymphatic pathway is affected in rodents with congenital hydrocephalus, and may very well present a target for novel therapeutic agents in hydrocephalus. Future studies along these lines are warranted.
The authors thank Mr. Arnell Sevilla for MRI imaging, Dr. Miles Johnston for advice in sample processing, and Vijay Pattisapu for technical assistance. The H-Tx colony was initially obtained from Dr. Hazel Jones.
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