CHOLINE ACETYLTRANSFERASE AS A THERAPY FOR HYPERTENSION

Abstract

Compositions and methods are provided comprising choline acetyltransferase (ChAT) and PEGylated ChAT for treating hypertension.

Claims

1. A method of reducing systemic hypertension in a subject in need thereof comprising administering to the subject a choline acetyltransferase (ChAT) or a ChAT conjugated to polyethylene glycol (PEG) in an amount and manner effective to reduce systemic hypertension in a subject.

2. The method of claim 1, wherein ChAT is conjugated to polyethylene glycol (PEG).

3. The method of claim 2, wherein ChAT is conjugated to 2-24 PEG chains.

4. The method of claim 2, wherein ChAT is conjugated to 12 PEG chains.

5. The method of claim 2, wherein each PEG chain has a molecular weight of 200-2,000 daltons.

6. The method of claim 1, wherein the subject is an adult human 18 years or older who prior to administration of ChAT or PEGylated ChAT had a resting systolic blood pressure at or above 130 mmHg and/or a diastolic blood pressure at or above 80 mmHg.

7. The method of claim 1, wherein the subject is an adult human 18 years or older who prior to administration of ChAT or PEGylated ChAT had a resting systolic blood pressure at or above 140 mmHg and/or a diastolic blood pressure at or above 90 mmHg.

8. The method of claim 1, wherein the subject has primary hypertension.

9. The method of claim 1, wherein the subject has secondary hypertension.

10. The method of claim 9, wherein the subject has narrowing of the arteries and/or chronic kidney disease.

11. The method of claim 1, wherein ChAT or PEGylated ChAT is administered by intravenous or intraperitoneal injection or via a pump.

12. The method of claim 1, wherein ChAT or PEGylated ChAT is administered by injections or infusions spaced over an interval of one or more days.

13. The method of claim 1, wherein ChAT or PEGylated ChAT is chronically administered via a pump.

14. The method of claim 1, wherein administration of ChAT or PEGylated ChAT is effective to reduce systolic blood pressure by at least 10 mmHg.

15. The method of claim 1, wherein administration of ChAT or PEGylated ChAT is effective to reduce systolic blood pressure by at least 20 mmHg.

16. The method of claim 1, wherein administration of ChAT or PEGylated ChAT is effective to reduce systolic blood pressure by at least 30 mmHg.

17. The method of claim 1, wherein administration of ChAT or PEGylated ChAT is effective to reduce systolic blood pressure by 10-40 mmHg.

18. The method of claim 1, wherein ChAT or PEGylated ChAT is human recombinant ChAT.

19. The method of claim 1, wherein ChAT or PEGylated ChAT is ChAT isoform R.

20. The method of claim 1, wherein the subject does not have any one or more of an age-related cognitive disorder, Alzheimer's disease, a neurodegenerative disease, amyotrophic lateral sclerosis, senile dementia, multi-infarct dementia, familial disautonomia, Huntington's disease, mental retardation, memory loss, myasthenia gravis, a gastrointestinal tract disorder, a spinal cord disorder, a brainstem disorders, a hypothalamic disorder, a limbic system disorder and dementia.

21. A pharmacological composition comprising choline acetyltransferase (ChAT) conjugated to polyethylene glycol (PEG) and a pharmaceutically acceptable carrier.

22. The pharmacological composition of claim 21, wherein ChAT is conjugated to 2-24 PEG chains.

23. The pharmacological composition of claim 21, wherein ChAT is conjugated to 12 PEG chains.

24. The pharmacological composition of claim 21, wherein each PEG chain has a molecular weight of 200-2,000 daltons.

25. The pharmacological composition of claim 21, wherein the PEGylated ChAT is formulated in dosage form for administration to a subject for treatment of hypertension.

26. The pharmacological composition of claim 21, wherein ChAT is human recombinant ChAT.

27. The pharmacological composition of claim 21, wherein ChAT is ChAT isoform R.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0007] FIG. 1A-1B. Single injection of ChAT decreases systolic blood pressure (SBP) in hypertensive mice. A) Minimum SBP during 12 hour post-injection period. B) Area-under-curve (AUC) of hypertensive-normalized SBP during 12 hour post-injection period. Histograms from left to right in each time period: Vehicle, 0.01 mg/kg, 0.1 mg/kg, 1 m/kg. For 1 mg/kg ChAT group, n=5. For 0.1 mg/kg ChAT and 0.01 mg/kg ChAT groups, n=4. For vehicle group, n=11. ** p<0.01.

[0008] FIG. 2A-2B. Chronic administration of ChAT using an osmotic pump decreases peak systolic blood pressure (SBP) in hypertensive animals. N=5 both groups; 3 days each condition. A) Vehicle-treated animals; B) ChAT-treated animals. *p<0.05; **p<0.01; ***p<0.001; ****p<0.0001; ns, not significant.

[0009] FIG. 3. Chronic administration of ChAT using an osmotic pump decreases peak systolic blood pressure in hypertensive animals. N=5 both groups; 3 days each condition.

[0010] FIG. 4A-4B. Chronic administration of ChAT using an osmotic pump decreases average systolic blood pressure in hypertensive animals. N=5 both groups; 3 days each condition. A) Vehicle-treated animals; B) ChAT-treated animals. *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.

[0011] FIG. 5. Chronic administration of ChAT using an osmotic pump decreases average systolic blood pressure in hypertensive animals. N=5 both groups; 3 days each condition.

[0012] FIG. 6. PEG-ChAT retains activity after PEGylation. PEG-ChAT and rChAT exceed the specific activity of commercially available rChAT. ****p<0.0001.

[0013] FIG. 7A-7D. A single injection of PEG-ChAT decreases systolic blood pressure (SBP) in hypertensive mice. A) PEG-ChAT was injected IP at the indicated doses at the black vertical line (time 0). For PEG-ChAT 1 mg/kg and 0.1 mg/kg, n=7. For vehicle, n=5. Traces from top to bottom at 1 hour post injection: vehicle, 0.1 mg/kg, 1 mg/kg. B) Minimum SBP during 12 hour post-injection period. C) Normotensive-normalized SBP during 12 hour post-injection period. Traces from top to bottom at 1 hour post injection: vehicle, 0.1 mg/kg, 1 mg/kg. D) Area-under-curve of hypertensive-normalized SBP during 12 hour post-injection period. For 1 mg/kg PEG-ChAT group, n=7. For 0.1 mg/kg PEG-ChAT group, n=7. For vehicle group, n=11. ** p<0.01; *** p<0.001.

[0014] FIG. 8A-8B. Daily doses of PEG-ChAT reduce SBP in hypertensive mice. A) SBP averaged during the active cycle for nocturnal mice (SBP.sub.12H-Dark) while normotensive, hypertensive, or post-PEG-ChAT injection. N; normotensive. H; hypertensive. The first injection occurred on day 1, and injections are represented by vertical dotted lines. Injections occurred on days 1, 2, and 3. B) Hypertensive index of mice during and after PEG-ChAT injections. To calculate the hypertensive index, first SBP is normalized to normotensive SBP. The AUC of this hypertensive-normalized SBP for a single day is calculated from a baseline of 1 (“AUC24”). The AUC24 is divided by AUC24-Hypertensive to generate the hypertensive index. A hypertensive index of 1 is equivalent to typical angiotensin II-induced hypertension as recorded before injections. A hypertensive index of 0 is normotensive as recorded before angiotensin II osmotic pump implant. Daily doses of 0.1 mg/kg PEG-ChAT produced a persistently lowered hypertensive index. For PEG-ChAT 1 mg/kg group, n=7; for PEG-ChAT 0.1 mg/kg group, n=9; for PEG-ChAT 0.01 mg/kg group, n=6; for vehicle group, n=2. ** p<0.01; *** p<0.001; **** p<0.0001.

DETAILED DESCRIPTION OF THE INVENTION

[0015] The present invention provides a method of reducing systemic hypertension in a subject in need thereof comprising administering to the subject choline acetyltransferase (ChAT) or ChAT conjugated to polyethylene glycol (PEG) in an amount and manner effective to reduce hypertension in a subject.

[0016] Preferably, the ChAT is human ChAT. The ChAT can be a recombinant ChAT. In one embodiment, the ChAT is ChAT isoform R.

[0017] The ChAT can be conjugated to polyethylene glycol (PEG). For example, ChAT can be conjugated to 2-24 PEG chains. In one embodiment, ChAT is conjugated to 12 PEG chains. Each PEG chain can have a molecular weight of, for example, 200-2,000 daltons. In one embodiment, PEG-ChAT has a molecular weight about 20,000 daltons greater than ChAT. Conjugation of PEG to ChAT can be effective to increase the solubility and/or half-life of ChAT.

[0018] The subject can be any mammal and is preferably a human. In one embodiment, the subject is an adult human 18 years or older who prior to administration of ChAT or PEGylated ChAT had a resting systolic blood pressure at or above 130 mmHg and/or a diastolic blood pressure at or above 80 mmHg. In one embodiment, the subject is an adult human 18 years or older who prior to administration of ChAT or PEGylated ChAT had a resting systolic blood pressure at or above 140 mmHg and/or a diastolic blood pressure at or above 90 mmHg. In one embodiment, the subject has primary hypertension. In one embodiment, the subject has secondary hypertension. In one embodiment, the subject has narrowing of the arteries and/or chronic kidney disease.

[0019] In one embodiment, the subject does not have any one or more of an age-related cognitive disorder, Alzheimer's disease, a neurodegenerative disease, amyotrophic lateral sclerosis, senile dementia, multi-infarct dementia, familial disautonomia, Huntington's disease, mental retardation, memory loss, myasthenia gravis, a gastrointestinal tract disorder, a spinal cord disorder, a brainstem disorders, a hypothalamic disorder, a limbic system disorder and dementia.

[0020] ChAT or PEGylated ChAT can be administered by any route known to those skilled in the art. In different embodiments, ChAT or PEGylated ChAT is administered by intravenous or intraperitoneal injection or infusion via a device such as an osmotic pump. In one embodiment, ChAT or PEGylated ChAT is administered by injections or infusions spaced over an interval of one or more days.

[0021] Preferably, administration of ChAT or PEGylated ChAT is effective to reduce systolic blood pressure by at least 10 mmHg, more preferably by at least 20 mmHg, and most preferably by at least 30 mmHg. In one embodiment, administration of ChAT or PEGylated ChAT is effective to reduce systolic blood pressure by 10-40 mmHg.

[0022] Also provided is a pharmacological composition comprising choline acetyltransferase (ChAT) conjugated to polyethylene glycol (PEG) and a pharmaceutically acceptable carrier. For example, ChAT can be conjugated to 2-24 PEG chains. In one embodiment, ChAT is conjugated to 12 PEG chains. Each PEG chain can have a molecular weight of, for example, 200-2,000 daltons. In one embodiment, PEG-ChAT has a molecular weight about 20,000 daltons greater than ChAT. The PEGylated ChAT can be formulated in dosage form for administration to a subject for treatment of hypertension.

[0023] Examples of acceptable pharmaceutical carriers include, but are not limited to, additive solution-3 (AS-3), saline, phosphate buffered saline, Ringer's solution, lactated Ringer's solution, Locke-Ringer's solution, Krebs Ringer's solution, Hartmann's balanced saline solution, and heparinized sodium citrate acid dextrose solution.

[0024] In an embodiment, human choline acetyltransferase has the following amino acid sequence (GenBank: AAA14245.1; SEQ ID NO:1):

TABLE-US-00001   1 mglrtakkrg lggggkwkre egggtrgrre vrpacflqsg grgdpgdvgg pagnpgcsph  61 praatrpppl pahtpahtpe wcgaasaeaa eprragphlc ipapgltktp ilekvprkma 121 aktpsseesg lpklpvpplq qtlatylqcm rhlvseeqfr ksqaivqqfg apgglgetlq 181 qkllerqekt anwvseywln dmylnnrlal pvnsspavif arqhfpgtdd qlrfaaslis 241 gvlsykalld shsiptdcak pelsgqplcm kqyyglfssy rlpghtqdtl vaqnssimpe 301 pehvivaccn qffvldvvin frrlsegdlf tqlrkivkma snederlppi glltsdgrse 361 waeartvlvk dstnrdsldm ierciclvcl dgpggvelsd thralqllhg ggysknganr 421 wydkslqfvv grdatcgvvc ehspfdgivl vqctehllkh mtqssrklir adsvselpap 481 rrlrwkcspe iqghlassae klqrivknld fivykfdnyg ktfikkqkcs pdafiqvalq 541 lafyrlhrrl vptyesasir rfqegrvdni rsatpealaf vravtdhkaa vpasekllll 601 kdairaqtay tvmaitgmai dnhllalrel aramckelpe mfmdetylms nrfvlstsqv 661 ptttemfccy gpvvpngyga cynpqpetil fcissfhsck etssskfaka veeslidmrd 721 lcsllpptes kplatkekat rpsqghqp.

[0025] In an embodiment, human choline acetyltransferase isoform R has the following amino acid sequence (GenBank: AAK08955.1; SEQ ID NO:2):

TABLE-US-00002   1 maaktpssee sglpklpvpp lqqtlatylq cmrhlvseeq frksqaivqq fgapgglget  61 lqqkllerqe ktanwvseyw lndmylnnrl alpvnsspav ifarqhfpgt ddqlrfaasl 121 isgvlsykal ldshsiptdc akgqlsgqpl cmkqyyglfs syrlpghtqd tlvaqnssim 181 pepehvivac cnqffvldvv infrrlsegd lftqlrkivk masnederlp piglltsdgr 241 sewaeartvl vkdstnrdsl dmierciclv cldapggvel sdthralqll hgggysknga 301 nrwydkslqf vvgrdgtcgv vcehspfdgi vlvqctehll khmtqssrkl iradsvselp 361 aprrlrwkcs peiqghlass aeklqrivkn ldfivykfdn ygktfikkqk cspdafiqva 421 lqlafyrlhr rlvptyesas irrfqegrvd nirsatpeal afvravtdhk aavpasekll 481 llkdairaqt aytvmaitgm aidnhllalr elaramckel pemfmdetyl msnrfvlsts 541 qvptttemfc cygpvvpngy gacynpqpet ilfcissfhs cketssskfa kaveeslidm 601 rdlcsllppt eskplatkek atrpsqghqp.

[0026] “And/or” as used herein, for example, with option A and/or option B, encompasses the separate embodiments of (i) option A, (ii) option B, and (iii) option A plus option B.

[0027] Where a numerical range is provided herein, it is understood that all numerical subsets of that range, and all the individual integers contained therein, are provided as part of the invention.

[0028] All combinations of the various elements described herein, including all subsets, are within the scope of the invention unless otherwise indicated herein or otherwise clearly contradicted by context.

[0029] This invention will be better understood from the Experimental Details, which follow. However, one skilled in the art will readily appreciate that the specific methods and results discussed are merely illustrative of the invention as described more fully in the claims that follow thereafter.

EXPERIMENTAL DETAILS

Methods and Materials

[0030] Animals. Male C57BL/6 mice were obtained from Jackson Laboratories (Bar Harbor, Me.) at 12 weeks of age. All mice were maintained in temperature-controlled rooms on a 12 h light-dark cycle with access to food and water ad libitum. Mice were singly housed after implanting blood pressure telemeters. All experimental protocols were approved by the Institutional Animal Care and Use Committee (IACUC) at the Feinstein Institutes for Medical Research (FIMR), Northwell Health, which follows the NIH guidelines for ethical treatment of animals.

[0031] Blood pressure measurements. Mice were induced under 2.5% isoflurane and implanted with HD-X10 blood pressure telemeters (DSI, New Brighton Minn.). A catheter was placed in the left carotid artery and advanced to the aortic arch. The telemeter body was placed in a subcutaneous pocket on the animal's flank, and blood pressure measurements were taken after an intervening period of 7 days.

[0032] Angiotensin II administration. Angiotensin II human (ThermoFisher) was purchased. Osmotic pumps (Alzet model 1004, Cupertino Calif., 95014) were loaded with angiotensin II in solution in varying concentrations to produce the desired flow rate (700-1500 ng/kg/min) and incubated in sterile saline at 37° C. for 48 hours before implantation. Mice were induced under 2.5% isoflurane anesthesia and a 1 cm mid-scapular incision was made. The pump was inserted and closed with a wound clip or sutures.

[0033] Production of recombinant ChAT protein. Recombinant human ChAT corresponding to residue 119-748 of respective protein (EC2.3.1.6) with a N-histidine tag was expressed in E. coli BL21 (Gold) DE3 cells. When bacteria were cultured to an A600 of 0.9, IPTG (isopropyl-1-thio-beta-D-galactopyranoside) was added to a final concentration of 3 mM to induce recombinant ChAT production. Bacteria were harvested and re-suspended in cold binding buffer and sonicated at 4° C. Cells debris was removed by centrifugation and the supernatant was applied onto a high affinity Ni-charged column pre-equilibrated with binding buffer. Following sequential washings the recombinant histidine-tagged ChAT protein was eluted with 0.5 M imidazole, 10% glycerol, 20% 1×DPBS. The recombinant ChAT was further purified by dialysis at 4° C. and extensive Triton X-114 extraction to remove contaminating endotoxins.

[0034] To increase the solubility and half-life of recombinant ChAT, unbranched amine-reactive MS(PEG)12 reagent (#22685, Thermo Scientific) was used to achieve the ChAT PEGylation. The reaction was performed in a buffer containing 10% glycerol, 20% DPBS 1×, 0.5 mM TCEP at a molar ratio of ChAT protein to MS(PEG)12 of 1 to 200-fold molar excess for 20 h at 4° C. Following PEGylation, the PEGylated protein was then dialyzed in buffer and further extracted with Triton X-114 to remove contaminating endotoxins.

[0035] ChAT activity assay. Activity of recombinant and PEGylated recombinant ChAT were analyzed using a colorimetric assay. ChAT and its substrates choline and acetyl-coenzyme A are incubated at 37° C. for 15 minutes. After incubation, a cocktail containing choline oxidase, 4-aminoantipyrine, phenol, and HRP is added. A red color develops in proportion to the choline remaining in the reaction mixture. By subtracting the remaining choline in wells containing ChAT from the choline remaining in a well without any enzyme, the reaction rate can be calculated.

[0036] Data Analysis. Data were analyzed using Graphpad Prism 7.0, Microsoft Excel, DSI Ponemah 6.4, and the R package “tidyverse”. Statistical significance was calculated using one-way ANOVA with Tukey's correction for multiple comparisons (e.g., FIG. 1A, FIG. 6, FIG. 7B) or with paired t-tests (e.g., FIG. 8A, FIG. 8B). In all figures, * p<0.05; ** p<0.01; *** p<0.001; **** p<0.0001.

Results

[0037] Administration of ChAT protein decreases blood pressure. An E. coli expression system was used to produce recombinant ChAT protein. Isoform R of ChAT was selected. The purified protein has a molecular weight of approximately 72 kDa. A colorimetric assay was used to determine the enzymatic activity of the recombinant protein. This ChAT protein has greater than 2-fold higher specific activity than commercially available ChAT (MyBioSource MBS653740) (FIG. 6). To examine the effects of ChAT administration in a murine model of hypertension, radiotelemetry was used to accurately monitor blood pressure (BP) in awake, free-moving mice. To induce hypertension, mice were implanted with osmotic pumps delivering a constant infusion of angiotensin II (700 ng/kg/min). After inducing hypertension, mice were injected intraperitoneally (i.p.) with ChAT and blood pressure was recorded. A single injection of ChAT decreased systolic blood pressure (SBP) (FIG. 1A). The minimum SBP after ChAT injection was significantly lower than injection of vehicle control. To calculate the duration of the effect, SBP was normalized to pre-injection SBP and area-under-the-curve (AUC) was calculated. SBP was decreased for 9 hours (FIG. 1B). For 1 mg/kg ChAT group, n=5. For 0.1 mg/kg ChAT and 0.01 mg/kg ChAT groups, n=4. For vehicle group, n=11.

[0038] Chronic administration of ChAT using an osmotic pump decreases peak, average and hourly systolic blood pressure in hypertensive animals. Animals were implanted with angiotensin-II osmotic pumps to induce hypertension after collecting 3 days of baseline BP data. After implanting angiotensin-II osmotic pumps, the animals recovered for 10 days before collecting hypertensive BP data. Twenty-five days after hypertensive BP data collection, the angiotensin-II pumps were replaced with new angiotensin-II pumps. During the angiotensin-II pump replacement surgery, animals also received an additional osmotic pump containing either saline (0.9%) or ChAT solution (3.4 mg/mL, 220 ng/kg/min), n=5 both groups. After 5 days of recovery, BP data were recorded for 3 days.

[0039] Peak systolic blood pressure (SBP) data were recorded for 3 days in the baseline, hypertensive and treated recording period. The average data are shown in FIG. 2A-2B. Treatment with the vehicle-dispensing pump does not decrease hypertensive peak SBP (FIG. 2A). Treatment with the ChAT-dispensing pump significantly decreases hypertensive peak SBP, returning it to baseline levels (FIG. 2B). The comparison between vehicle and pump treated groups is shown in FIG. 3. During the baseline and hypertensive recording sessions, there was no difference in peak SBP between groups. During the treatment recording session, ChAT-dispensing pump treatment significantly decreased peak SBP compared to vehicle treatment. Data were analyzed using 2-way ANOVA with multiple comparisons, corrected using Tukey's test.

[0040] Chronic administration of ChAT using an osmotic pump decreases average SBP in hypertensive animals (FIG. 4A-4B). SBP was averaged over the 72 hours during each recording session. Treatment with the vehicle-dispensing pump does not decrease hypertensive average SBP (FIG. 4A). Treatment with the ChAT-dispensing pump significantly decreases hypertensive average SBP, returning it to baseline levels (FIG. 4B). The comparison between vehicle and pump treated groups is shown in FIG. 5. During the baseline and hypertensive recording sessions, there was no difference in average SBP between groups. During the treatment recording session, ChAT-dispensing pump treatment significantly decreases average SBP compared to vehicle treatment. Data were analyzed using 2-way ANOVA with multiple comparisons, corrected using Tukey's test. Chronic administration of ChAT using an osmotic pump also decreases hourly systolic BP.

[0041] PEGylated ChAT leads to greater reductions in blood pressure than rChAT. To increase the duration of the effect of recombinant ChAT administration, ChAT was PEGylated to create PEGylated recombinant ChAT (PEG-ChAT). PEGylation increases hydrodynamic radius and immunogenicity, leading to more durable biologic molecules with longer lasting biological effects. The molecular weight of PEG-ChAT was approximately 95 kDa, a ˜20 kD increase compared to rChAT. PEG-ChAT has comparable specific activity to rChAT, which is significantly higher than commercially available rChAT (FIG. 6). After inducing hypertension, mice were injected i.p. with PEG-ChAT. A single injection of PEG-ChAT produces decreases in blood pressure in a dose-dependent manner (FIG. 7A-7B). A single PEG-ChAT injection was able to decrease SBP to normotensive levels despite the animals being hypertensive before injection (FIG. 7C), and area-under-the-curve analysis again normalized to hypertensive SBP showed a duration of effect of 12 hours (FIG. 7D). For 1 mg/kg PEG-ChAT group, n=7. For 0.1 mg/kg PEG-ChAT group, n=7. For vehicle group, n=11.

[0042] Repeated doses of PEGylated ChAT lead to long-lasting effects. Since a single dose of PEG-ChAT produced larger decreases in blood pressure than rChAT, the duration of this effect was increased by injecting PEG-ChAT once per day for multiple consecutive days utilizing the same hypertension model. Normotensive and hypertensive SBP were measured for all animals before injections. SBP was averaged during the period when room lights are off (SBP.sub.12H-Dark), as that is the active cycle for nocturnal mice. Multiple injections of PEG-ChAT significantly decreased SBP SBP.sub.12H-Dark for a week post-injection (FIG. 8A). SBP was normalized to normotensive SBP and averaged hourly, showing that injections of 0.1 mg/kg could decrease SBP close to normotensive levels. To further characterize the decrease in blood pressure, a “hypertensive index” was developed for the murine hypertension model. To calculate the hypertensive index, first systolic blood pressure (SBP), recorded after angiotensin II pump implant but before injections, was normalized to normotensive SBP. The area under the curve (AUC) of this normotensive-normalized SBP for a single day was calculated from a baseline of 1 (“AUC24-Hypertensive”). This AUC24-Hypertensive value is an indication of the severity of hypertension and is dependent on the response to angiotensin II infusion. Calculating this value allows for the elimination of differential responses to angiotensin II between experimental groups. SBP recorded during and after injections is also normalized to normotensive SBP. The AUC of this normotensive-normalized SBP for a single day is calculated from a baseline of 1 (“AUC24”). The AUC24 is divided by AUC24-Hypertensive to generate the hypertensive index. A hypertensive index of 1 is equivalent to typical angiotensin II-induced hypertension as recorded before injections. A hypertensive index of 0 is normotensive as recorded before angiotensin II osmotic pump implant. Daily doses of 0.01 and 0.1 mg/kg PEG-ChAT produced a persistently lowered hypertensive index, with 0.1 mg/kg PEG-ChAT doses having a greater effect (FIG. 8B). For 1 mg/kg PEG-ChAT group, n=7. For 0.1 mg/kg PEG-ChAT group, n=9. For 0.01 mg/kg PEG-ChAT group, n=5. For vehicle group, n=2.

REFERENCES

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