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Acta Pharmacologica Sinica logoLink to Acta Pharmacologica Sinica
. 2011 Jun 3;32(6):845–852. doi: 10.1038/aps.2011.43

Enhanced salt sensitivity following shRNA silencing of neuronal TRPV1 in rat spinal cord

Shuang-quan Yu 1, Donna H Wang 1,2,*
PMCID: PMC4009958  PMID: 21642952

Abstract

Aim:

To investigate the effects of selective knockdown of TRPV1 channels in the lower thoracic and upper lumbar segments of spinal cord, dorsal root ganglia (DRG) and mesenteric arteries on rat blood pressure responses to high salt intake.

Methods:

TRPV1 short-hairpin RNA (shRNA) was delivered using intrathecal injection (6 μg·kg−1·d−1, for 3 d). Levels of TRPV1 and tyrosine hydroxylase expression were determined by Western blot analysis. Systolic blood pressure and mean arterial pressure (MAP) were examined using tail-cuff and direct arterial measurement, respectively.

Results:

In rats injected with control shRNA, high-salt diet (HS) caused higher systolic blood pressure compared with normal-salt diet (NS) (HS:149±4 mmHg; NS:126±2 mmHg, P<0.05). Intrathecal injection of TRPV1 shRNA significantly increased the systolic blood pressure in both HS rats and NS rats (HS:169±3 mmHg; NS:139±2 mmHg). The increases was greater in HS rats than in NS rats (HS: 13.9%±1.8%; NS: 9.8±0.7, P<0.05). After TRPV1 shRNA treatment, TRPV1 expression in the dorsal horn and DRG of T8-L3 segments and in mesenteric arteries was knocked down to a greater extent in HS rats compared with NS rats. Blockade of α1-adrenoceptors abolished the TRPV1 shRNA-induced pressor effects. In rats injected with TRPV1 shRNA, level of tyrosine hydroxylase in mesenteric arteries was increased to a greater extent in HS rats compared with NS rats.

Conclusion:

Selective knockdown of TRPV1 expression in the lower thoracic and upper lumbar segments of spinal cord, DRG, and mesenteric arteries enhanced the prohypertensive effects of high salt intake, suggesting that TRPV1 channels in these sites protect against increased salt sensitivity, possibly via suppression of sympatho-excitatory responses.

Keywords: blood pressure, high salt intake, intrathecal injection, short-hairpin RNA, sympathetic nerve, TRPV1

Introduction

Accumulating evidence indicates that sensory nerves play a key role in regulating blood pressure1, 2, 3. The transient receptor potential vanilloid type 1 (TRPV1) channel is abundantly expressed in sensory nerves4, 5 and conveys the intricate task of modulating the function of these nerves. Thus, defining the role of TRPV1-positive sensory nerves in the regulation of blood pressure and salt sensitivity will be useful. We have shown previously that the degeneration of TRPV1-expressing sensory nerves throughout the neonatal body by subcutaneous injection of capsaicin, a selective TRPV1 agonist, leads to increased salt sensitivity of arterial pressure, indicating that TRPV1-positive sensory nerves play a counter-regulatory role against salt-induced increases in blood pressure6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20. The underlying mechanism of anti-hypertensive effects of TRPV1 may involve its counter-balancing role against the activation of the renin-angiotensin-aldosterone system7, 8, 9, sympathetic nervous system10, endothelin system11, 12, superoxide generation system13, 14, and epithelial sodium transporters15. Our previous approach using systemic sensory denervation does, however, have two major limitations. First, systemic sensory denervation obliterates not only TRPV1 but also other components that colocalize with TRPV1 in the same neuron, which may regulate blood pressure independently of TRPV121, 22. Second, systemic sensory denervation prevents elucidation of the role of specific organ(s) or tissue(s) in regulating blood pressure.

To bypass these limitations, we developed a new model with improved approaches and validation. We applied TRPV1 shRNA to selectively knock down TRPV1 expression without affecting other components that colocalize with TRPV1 in the same neuron. The strategy of using shRNA to selectively silence TRPV channels in vivo has been successfully used in our previous study to effectively knock down the expression and function of TRPV4 channels23. In the present study, we used an intrathecal injection technique to target the T8-L3 segments of the dorsal root ganglia (DRG) and their central (dorsal horn) and peripheral (mesenteric arteries and kidneys) terminals without affecting other regions. The T8-L3 segments were chosen as targets because they innervate mesenteric resistance arteries and the kidneys, which are known for their involvement in blood pressure regulation24, 25, 26, 27, 28, 29.

Using this strategy, we sought to determine whether selective knockdown of TRPV1 expressed in DRG of lower thoracic and upper lumbar segments (T8-L3) and their central and periphery projections enhances the prohypertensive effects induced by salt loading. Furthermore, to assess whether the sympathetic nervous system is involved in TRPV1 shRNA-induced blood pressure regulation, the content of tyrosine hydroxylase (TH), a marker of sympathetic nerves, and blood pressure responses to prazosin, a blocker of α1-adrenoceptors, were examined.

Materials and methods

Animals

Male Wistar rats (201−225 g, Charles River Laboratory, Wilmington, Massachusetts, USA) were housed in a standard facility. Rats received either a normal-salt (NS) diet (1% NaCl by weight, Harlan Teklad, Madison, Wisconsin, USA) or a high-salt (HS) diet (8% NaCl by weight, Harlan Teklad, Madison, Wisconsin, USA). One week after dietary treatment, rats underwent surgery for intrathecal catheter implantation and removal of the right kidney. One week after surgery, rats began receiving intrathecal injections of either TRPV1 shRNA or control shRNA once per day for 3 d and were randomly divided into 4 groups: NS diet+control shRNA, NS diet+TRPV1 shRNA, HS diet+control shRNA, or HS diet+TRPV1 shRNA. Measurement of systolic blood pressure, mean arterial pressure, water intake, and urine excretion and tissue sample collection for immunohistochemistry and Western blot analysis were performed on d 3 after the beginning of shRNA treatment. All experiments were performed in accordance with the protocols approved by the Institutional Animal Care and Use Committee of Michigan State University.

Surgery for intrathecal catheter implantation and uninephrectomy

Under anesthetization with ketamine/xylazine (85/5 mg/kg, ip), the nape skin was cut open and a small incision was made in the atlanto-occipital membrane. The muscles were separated, and a PE-10 catheter was inserted into the subarachnoid space as far as the T8 segment of the spinal cord (the length of the catheter from the inside end to the atlanto-occipital membrane was about 7.5 cm) and sutured in place, and the incision was closed. About 5 cm of the catheter remained external for injection of shRNA and was sealed with parafilm to stop the outflow of cerebrospinal fluid when not used for injection. Uninephrectomy was performed by making a right flank incision and then removing the right kidney.

Preparation of TRPV1 shRNA or control shRNA and intrathecal injection

TRPV1 shRNA or control shRNA (KR42959N, SABiosciences, Frederick, Maryland, USA) were mixed with i-Fect™ (NI35150, Neuromics, Edina, Minnesota, USA) in a 1:5 ratio (w/v) for intrathecal injection. Rats received 6 μg/kg in a 10-μL volume of either TRPV1 shRNA or control shRNA once daily for three consecutive days. The catheter was immediately flushed with 10 μL of saline following every injection to ensure that all drugs reached the subarachnoid space.

Measurements of systolic blood pressure, water intake, and urine excretion

Systolic blood pressure of conscious rats was measured by the indirect tail-cuff method with a sphygmomanometer (Hatteras Instruments, Cary, North Carolina, USA). Rats were accustomed to the testing environment for 3 d prior to the measurement, and the blood pressure value for each rat was calculated as the average of nine separate measurements. Twenty-four-hour water intake and urine excretion were determined by the use of metabolic cages one day before and three days after intrathecal injection.

Measurement of mean arterial pressure (MAP) and its response to intravenous injection of capsaicin

The jugular vein and carotid artery of pentobarbital (50 mg/kg, ip) anesthetized rats were cannulated for administration of capsaicin (30 μg/kg, Sigma, M2028, dissolved in saline with 0.1% ethanol) and for monitoring of MAP (Gould Instruments, Valley View, Ohio, USA), respectively. MAP was recorded 30 min after the cannulation and recorded every 3 s. The MAP value for each rat was calculated as the average of 10 min of continuous measurements.

Blockade of α1-adrenoceptor by prazosin

Prazosin (P7791, Sigma-Aldrich, St Louis, Missouri, USA, dissolved in saline), an α1-adrenoceptor blocker, was intragastrically administered via gavage, at a dose of 0.5 mg/kg of each administration dose, twice per day for 7 d starting 3 d before shRNA injection.

Immunohistochemistry

For TRPV1 staining, samples of the spinal cord and DRG of T8-L3 segments, mesenteric arteries, and kidneys were fixed in 4% paraformaldehyde dissolved in phosphate-buffered saline and then cut into 20-μm sections using a cryostat (Leica CM 1850, Leica Biosystems Nussloch GmbH, Nussloch, Germany). The sections were incubated with guinea pig anti-TRPV1 polyclonal antibody (1:500, AB5566, Millipore, Billerica, Massachusetts, USA) for 1 h at room temperature, and then they were incubated with rhodamine redTM-X donkey anti-guinea pig IgG (1:100, 711-295-152, Jackson ImmunoResearch Laboratories, West Grove, Pennsylvania, USA) for 1 h at room temperature. Pictures were taken with a fluorescent microscope (Olympus BX41 model, Olympus Optical Co, Ltd, Tokyo, Japan; Olympus MicroSuiteTM-Basic software, Olympus Soft Imaging Solutions GmbH, Münster, Germany).

For tyrosine hydroxylase staining, whole-mount mesenteric second-order arteries were fixed in 70% acetone (in saline) for 3 h. The primary antibody was mouse anti-TH monoclonal antibody (1:1000, Calbiochem 657010, EMD Chemicals, Gibbstown, New Jersey, USA, 1:1000, 1 h at room temperature), and the secondary antibody was rhodamine redTM-X donkey anti-mouse IgG (1:100, 715-295-151, Jackson ImmunoResearch Laboratories, West Grove, Pennsylvania, USA, 1 h at room temperature).

Western blot analysis

Samples were homogenized in 10 mmol/L Tris buffer (pH 7.6) that included protein inhibitors. After centrifugation at 500×g for 5 min, the supernatant was added to 20 μL of 0.5 mol/L EDTA and centrifuged at 50 000×g for 1 h. The pellet was resuspended with lysis buffer on ice for 45 min and centrifuged at 14 000× g for 20 min. After denaturation for 10 min at 100 °C, 30 μg protein of each supernatant was electrophoresed on a 10% SDS-PAGE gel and transferred to a PVDF membrane (162-0180, Bio-Rad Laboratories, Hercules, California, USA). Membranes were incubated with rabbit anti-TRPV1 (1:1000, PA1-29421, Affinity BioReagents, Golden, Colorado, USA) or mouse anti-TH (1:1000, 657010, Calbiochem, EMD Chemicals Inc, Gibbstown, New Jersey, USA) at 4 °C overnight, followed by incubation with HRP-donkey anti-rabbit IgG (1:10 000, 711-035-152, Jackson ImmunoResearch Laboratories, West Grove, Pennsylvania) or HRP-donkey anti-mouse IgG (1:10 000, 711-035-151, Jackson ImmunoResearch Laboratories, West Grove, Pennsylvania, USA) for 2 h at room temperature. The intensity of the bands was determined using ImageJ software (NIH, Bethesda, Maryland, USA). Protein loading on the membrane was normalized to β-actin (mouse anti-β-actin monoclonal antibody, 1:1000, sc-69879, Santa Cruz Biotechnology, Santa Cruz, California, USA).

Statistical analysis

Data are expressed as mean±SEM. Differences between paired groups were analyzed using an unpaired Student's t-test. Differences among groups were analyzed using a one-way ANOVA followed by a Bonferroni adjustment for multiple comparisons. Differences were considered statistically significant at P<0.05.

Results

Body weight in all groups increased with age. No difference in body weight was found between NS and HS diet-treated rats administered control or TRPV1 shRNA before dietary treatment, at the day of intrathecal injection, or 3 d after intrathecal injection (data not shown), which indicates that the general growth and condition of the rats were not affected by dietary or intrathecal treatment.

TRPV1 shRNA treatment resulted in a greater pressor effect in HS rats compared with NS rats

HS diet intake for 2 weeks, without shRNA treatment, increased systolic blood pressure when compared with NS-treated rats (Figure 1A). Systolic blood pressure was elevated 3 d after intrathecal injection of TRPV1 shRNA in both NS- and HS-treated rats (in NS rats, control shRNA: 126±2 vs TRPV1 shRNA: 139±2 mmHg, P<0.05; in HS rats, control shRNA: 149±4 vs TRPV1 shRNA: 169±3 mmHg, P<0.05, Figure 1A). Moreover, the increases in systolic blood pressure after TRPV1 shRNA treatment were greater in HS- than in NS-treated rats (NS: 9.8%±0.7% vs HS: 13.9%±1.8%, P<0.05, Figure 1B).

Figure 1.

Figure 1

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Effects of intrathecal injection of TRPV1 shRNA on systolic blood pressure in rats fed a normal-sodium (NS) or high-sodium (HS) diet. (A) The systolic blood pressure at d 3 after control or TRPV1 shRNA treatment. (B) The percentage change in systolic blood pressure of TRPV1 shRNA compared to that of corresponding control shRNA. Values are expressed as mean±SEM (n=11 to 14). bP<0.05 compared with the corresponding control shRNA-treated group; eP<0.05 compared with the corresponding NS diet group.

TRPV1 shRNA treatment led to greater TRPV1 downregulation in targeted tissues in HS rats compared with NS rats

Immunohistochemistry studies revealed that TRPV1 expression in the dorsal horn of the spinal cord (T8-L3 segments), DRG (T8-L3 segments), and mesenteric arteries was attenuated in TRPV1 shRNA-treated rats fed either an NS or a HS diet compared with corresponding control shRNA-treated rats (Figure 2). Consistently, quantitative measurement of TRPV1 content by Western blot analysis revealed that TRPV1 expression was knocked down by TRPV1 shRNA treatment in both NS rats and HS rats in the dorsal horn of the spinal cord (T8-L3 segments), DRG (T8-L3 segments), and mesenteric arteries (Figure 3). Western blot analysis revealed that TRPV1 expression was also knocked down by TRPV1 shRNA in the kidney (NS, control shRNA: 0.37±0.02 vs TRPV1 shRNA: 0.29±0.01, P<0.05; HS, control shRNA: 0.50±0.03 vs TRPV1 shRNA: 0.29±0.02, P<0.05). In contrast, no significant change was found in TRPV1 levels in the cervical spinal cord in NS or HS rats after TRPV1 shRNA treatment (NS, control shRNA: 0.35±0.02 vs TRPV1 shRNA: 0.32±0.03, P>0.05; HS, control shRNA: 0.45±0.01 vs TRPV1 shRNA: 0.44±0.02, P>0.05), indicating that shRNA suppression occurred only in the targeted segments/tissues. Moreover, TRPV1 expression in the dorsal horn, DRG, and mesenteric arteries was higher in HS rats administered control shRNA compared with NS rats given control shRNA, and the magnitude of TRPV1 down-regulation by TRPV1 shRNA treatment was greater in HS than in NS rats (dorsal horn, NS: -32%±3% vs HS: -48%±6%, P<0.05; DRG, NS: -28%±3% vs HS: -44%±5%, P<0.05; mesenteric arteries, NS: -28%±4% vs HS: -50%±5%, P<0.05).

Figure 2.

Figure 2

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Immunohistochemistry staining showing TRPV1 expression in the dorsal horn of the spinal cord (T8-L3), dorsal root ganglia (DRG) (T8-L3) and mesenteric arteries (MA) of rats fed a NS or HS diet 3 d after control or TRPV1 shRNA treatment. Scale bars, 100 μm.

Figure 3.

Figure 3

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Western blot analysis showing TRPV1 expression in the dorsal horn of the spinal cord (T8-L3), DRG (T8-L3), and mesenteric arteries of rats fed a NS or HS diet 3 d after control or TRPV1 shRNA treatment. The left, middle, and right panels indicate representative Western blots, quantification results (β-actin arbitrary units), and the percentage change of TRPV1 expression of TRPV1 shRNA from that of corresponding control shRNA, respectively. Values are expressed as mean±SEM (n=5). bP<0.05 compared with the corresponding control shRNA-treated group; eP<0.05 compared with the corresponding NS diet group.

TRPV1 shRNA treatment resulted in a greater degree of inhibition of capsaicin-induced depressor effects in HS rats compared with NS rats

To further confirm TRPV1 suppression induced by TRPV1 shRNA, we examined blood pressure responses to iv injection of capsaicin, a selective TRPV1 agonist. The magnitude of the prolonged depression phase of MAP in response to capsaicin was attenuated in both NS and HS rats (Figure 4A) that received TRPV1 shRNA compared with rats that received control shRNA. The magnitude of inhibition of capsaicin-induced depressor effects by TRPV1 shRNA treatment was greater in HS rats than in NS rats (NS: -34%±3% vs HS: -50%±3%, P<0.05) (Figure 4B).

Figure 4.

Figure 4

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The response of mean arterial pressure (MAP) at 36 s to a bolus injection of capsaicin (30 μg/kg, iv) in NS rats and HS rats 3 d after administration of control or TRPV1 shRNA (A) and the percentage change of MAP in response to capsaicin following TRPV1 shRNA compared with corresponding control shRNA (B). Values are expressed as mean±SEM (n=6 to 7). bP<0.05 compared with the corresponding control shRNA-treated group; eP<0.05 compared with the corresponding NS diet group.

TRPV1 shRNA treatment had no effect on urinary excretion in HS- or NS-treated rats

HS intake increased urine excretion, water intake, and the ratio of urine/water intake compared with NS-treated rats both before shRNA treatment and 3 d after. However, no significant differences were found between control shRNA and TRPV1 shRNA-treated rats fed a NS or HS diet in 24-h urine excretion (NS rats, control shRNA: 30±1 vs TRPV1 shRNA: 27±2 mL, P>0.05; HS rats, control shRNA: 106±7 vs TRPV1 shRNA: 106±9 mL, P>0.05), 24-h water intake (NS rats, control shRNA: 53±2 vs TRPV1 shRNA: 50±4, P>0.05; HS rats, control shRNA: 135±9 vs TRPV1 shRNA: 131±10, P>0.05), or the ratio of 24-h urine/water intake (NS rats, control shRNA: 0.58±0.02 vs TRPV1 shRNA: 0.54±0.02, P>0.05; HS rats, control shRNA: 0.79±0.01 vs TRPV1 shRNA: 0.80±0.02, P>0.05).

Depressor effects induced by blockade of α1-adrenoceptors following treatment with TRPV1 shRNA were greater in HS rats compared with NS rats

In both NS and HS rats, blockade of the α1-adrenoceptor by prazosin pretreatment prevented TRPV1 shRNA-induced elevation of blood pressure (Figure 5A). Moreover, prazosin played a greater depressor role in HS-treated rats given TRPV1 shRNA compared with NS-treated rats given TRPV1 shRNA (NS: -7%±1% vs HS: -12%±1%, P<0.05, Figure 5B).

Figure 5.

Figure 5

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Pretreatment with prazosin prevented TRPV1 shRNA-induced elevation of blood pressure in rats fed NS or HS diets (A) and the percentage change of systolic blood pressure induced by prazosin compared with controls that did not receive prazosin (B). Values are expressed as mean±SEM (n=6 to 7). bP<0.05 compared with the corresponding control shRNA-treated group; eP<0.05 compared with the corresponding NS diet group; hP<0.05 compared with the corresponding “without prazosin group.”

TRPV1 shRNA treatment led to enhanced upregulation of mesenteric tyrosine hydroxylase in HS rats compared with NS rats

Immunohistochemistry staining (Figure 6A) and Western blot analysis (Figure 6B) revealed that TH levels in mesenteric arteries were enhanced in both NS and HS rats administered TRPV1 shRNA treatment compared with corresponding control shRNA-treated rats. In control shRNA-treated rats, HS intake increased TH expression in mesenteric arteries compared with the NS diet. TRPV1 shRNA treatment produced a greater increase in TH in HS rats than in NS rats (NS: 46%±9% vs HS: 77%±6%, P<0.05) (Figure 6B). In contrast, no significant differences were found in TH levels in the kidney in NS or HS rats administered TRPV1 shRNA compared with rats receiving the control shRNA (NS, control shRNA: 0.22±0.01 vs TRPV1 shRNA: 0.24±0.01, P>0.05; HS, control shRNA: 0.25±0.02 vs TRPV1 shRNA: 0.30±0.02, P>0.05).

Figure 6.

Figure 6

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Immunohistochemistry staining (A) and Western blot analysis (B) showing tyrosine hydroxylase expression in mesenteric arteries of rats fed a NS or HS diet 3 d after either control or TRPV1 shRNA treatment. The left, middle, and right panels in (B) indicate representative Western blots, quantification results (% β-actin arbitrary units), and the percentage change of TH expression in rats receiving TRPV1 shRNA compared with control shRNA, respectively. Values are expressed as mean±SEM (n=5). bP<0.05 compared with the corresponding control shRNA-treated group; eP<0.05 compared with the corresponding NS diet group. Scale bars, 100 μm.

Discussion

The goal of this study was to determine whether selective knockdown of TRPV1 expressed in the DRG of lower thoracic and upper lumbar segments (T8-L3) and their central and periphery projections enhances prohypertensive effects induced by salt loading. We observed that (1) TRPV1 shRNA treatment increased blood pressure to a greater extent in HS rats compared with NS rats; (2) HS diet enhanced TRPV1 expression in the dorsal horn, DRG, mesenteric arteries, and kidneys, which was suppressed by TRPV1 shRNA treatment; (3) TRPV1 shRNA treatment attenuated the depressor action of capsaicin with a greater effect in HS rats compared with NS rats; (4) TRPV1 shRNA treatment had no effect on urinary excretion, water intake, or the ratio of urine/water intake in rats fed a NS or HS diet; (5) blockade of α1-adrenoceptors led to a greater depressor effect in HS rats compared with NS rats treated with TRPV1 shRNA; and (6) TRPV1 shRNA treatment produced a greater increase in TH in mesenteric arteries, but not kidneys, in HS rats compared with NS rats. These data show that selective knockdown of neuronal TRPV1 enhances prohypertensive effects induced by salt loading and that pressor effects of TRPV1 shRNA may be mediated, at least in part, by enhancement of the sympatho-excitatory response.

We have previously shown that neonatal degeneration of TRPV1-expressing sensory nerves increased salt sensitivity of arterial pressure as these rats grew into adulthood6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20. However, the systemic sensory denervation used in these previous studies precluded us from making conclusions about whether the observed effect was due to the removal of TRPV1 or other proteins co-expressed in the same nerves innervating any specific organs or tissues21, 22. In the present study, we anatomically limited the TRPV1 affected by intrathecally injecting TRPV1 shRNA to selectively knockdown TRPV1 in an attempt to answer the question of whether impairment of TRPV1 in selective tissues is sufficient to enhance salt sensitivity of blood pressure. shRNA knocks down the expression of a specific gene by RNA interference, and its transfection efficacy can be further enhanced by the use of the transfection reagent iFect™, which is particularly designed for facilitating effective transfection for neuronal cells. We did not observe any neuron damage or other side effects following intrathecal injection of shRNA (data not shown), which is consistent with observations made by other laboratories30. Our results show that knocking down TRPV1 expression in T8-L3 DRG and their central and periphery projections, without affecting other segments such as the cervical spinal cord, significantly modulated the development of hypertension, especially during salt loading. These results indicate that intrathecal injection with shRNA is a viable strategy of conditional knockdown, which can be used to study the role of a given gene or protein.

Although TRPV1 expression in the kidney was suppressed, no changes occurred for 24-h urine excretion, water intake, or the ratio of urine/water intake after TRPV1 shRNA treatment. Although unexpected, these results suggest that mechanisms other than altered renal function are responsible for the prohypertensive effect of TRPV1 shRNA. Given that the peripheral projections of T8-L3 DRGs innervate mesenteric arteries, we examined mesenteric TRPV1 levels. Indeed, TRPV1 levels in mesenteric resistant arteries were suppressed by TRPV1 shRNA treatment. Interestingly, levels of tyrosine hydroxylase, a sympathetic nerve marker, were markedly upregulated after TRPV1 shRNA treatment in mesenteric resistant arteries but not kidneys. Furthermore, blockade of α1-adrenoceptors completely abolished TRPV1 shRNA-induced prohypertensive effects. These data suggest that heightened sympathetic nerve activity occurred, which contributed to TRPV1 shRNA-induced hypertension. The pressor effect of TRPV1 shRNA may be mediated by enhanced vasoconstriction of mesenteric resistant arteries via at least two potential mechanisms. First, knockdown of TRPV1 in the dorsal horn would decrease signal input from periphery organs to the central nervous system via afferent primary neurons and, as a result, diminish the inhibitory effect of afferent nerves on sympathetic nerve activity in mesenteric resistant arteries31, 32, 33, 34. Second, knockdown of TRPV1 expressed in mesenteric resistant arteries would reduce the release of vasodilator neuropeptides such as CGRP and, as a result, diminish the counter-regulatory role of afferent nerves against vasoconstriction24, 35, 36.

Our data show that HS intake led to compensatory increases in mesenteric TRPV1 levels, which is consistent with previous reports36, 37, 38. Moreover, the depressor effect of TRPV1 activation after capsaicin administration was much greater in HS rats compared with NS rats, supporting the notion that TRPV1 plays a counter-regulatory role against salt-induced increases in blood pressure. The counter-regulatory effect of TRPV1 has been shown to involve enhanced CGRP release from sensory nerves that cause vasodilation, sodium and water excretion, and decreases in blood pressure39, 40, 41, 42, 43. TRPV1 shRNA treatment resulted in enhanced suppression of mesenteric TRPV1 levels but enhanced up-regulation of mesenteric tyrosine hydroxylase contents. The combination of these effects would lead to a more pronounced pressor action in HS rats. Indeed, as shown in the present study, HS rats displayed a greater degree of pressor effects after TRPV1 shRNA treatment when compared with NS rats receiving the same treatment.

In conclusion, the present study shows that intrathecal injection of TRPV1 shRNA selectively knocks down TRPV1 expression in the DRG of T8-L3 segments and their central and periphery projections in rats, which enhances the prohypertensive effects induced by salt loading. The pressor effect of TRPV1 shRNA may be mediated, at least in part, by enhancement of the sympatho-excitatory response.

Author contribution

Donna H WANG designed research, secured funding, and interpreted the data; Shuang-quan YU performed the experiments and analyzed the data; Donna H WANG and Shuang-quan YU wrote the paper.

Acknowledgments

This work was supported in part by the NIH (grants HL-57853, HL-73287, and DK67620).

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